Genetics Learning Material (Midterm)
Genetics Learning Material (Midterm)
The content of this handout is based from the books of the following authors who are
being acknowledged:
Alberts B., Bray D., Hopkin K., Johnson A., Lewis J., Raff M., Roberts K., Walter
P. 2013. Essential Cell Biology, 4th Edition. London: Garland Science.
Clark, M., Choi, J., Douglas, M., 2018. Biology 2e. 2nd edition. OpenStax. Houston
Texas 7705. Rice University.
Griffiths AJ., Miller JH., Suzuki DT., Lewontin RC., Gelbart, eds. 2000. An
Introduction to Genetic Analysis. 7th ed. New York: W. H. Freeman.
King RC., Mulligan PK., Stansfield WD. 2013. A Dictionary of Genetics. 8th ed.
New York: Oxford University Press.
Smith, J. 2012. General, organic, and biological chemistry (2nd ed.). Boston:
McGraw-Hill Companies.
Urry, LA., Cain, ML., Wasserman, SA., Minorsky, PV., Reece, JB. 2017.
Campbell Biology. 11th edition. United States of America. Pearson
Higher Education.
This material is intended for instructional purposes only. It is not intended for sale.
Should it be distributed to persons other those enrolled in this subject or be dispended for
commercial purposes, the university and the faculty member will not be responsible for any
claims of the original authors.
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Preface
With the present COVID crisis, achieving the goal to deliver the lessons effectively is
even a greater challenge. In this online learning scheme, this instructional material was made
simplified but comprehensive for students’ use. This is a student-centered instructional
material which aims to promote an independent learning approach to develop students’ critical
thinking, hone their skills in decision-making and solving problems, and instill to them the
positive attitudes and values.
---oOo---
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OVERVIEW
iv
Educ Sci 323A Genetics is a 4-unit course which is divided into two parts: (I)
Genetics (Lecture), a 3-unit course; and (II) Genetics (Laboratory), a 1-unit course.
Course Description
This course deals with the principles of heredity and variation; its application in
plant and animal breeding, and problems involved in it. It also includes biometrical
treatment of qualitative and quantitative characters of both plants and animals.
Course Outline
Midterm Coverage:
Unit 1: Introduction to Genetics
Unit 2: Meiosis and Sexual Life Cycles
Unit 3: Mendelian Genetics
Final Coverage
Unit 4: Extending Mendelian Genetics
Unit 6: Gene Function
Unit 7: Genetic Engineering and Biotechnology
Each unit has subtopics. For more details, please see Contents.
Course Outcomes
Time Frame
The suggested allotted time to finish all the lessons is 54 hours (12 weeks)—that
includes the readings and answering of all the activities and assessments. There are 6
units for the subject: three (3) units for the mid-term and three (3) units for the final
term. The first three units (for midterm) has a suggested time allotment of 6 weeks.
The next three (3) units (Final term) has a time allotment of 6 weeks. Each unit (e.g.,
Unit 1) is expected to be finished within 2 weeks. Please see the number of hours
allotted per lesson in the Contents. These are just suggested time frames. You are free
to use on what day you are going to answer all activities.
NOTE: If you use your time wisely, it is possible for you to finish all the lessons within
the suggested time allotment.
vi
Course Policies
1. Take care of the hand outs for the interests of the next users.
2. Return handouts during or after midterm examination.
3. Do not write on the handouts. Use the separate sheets for all exercises. Consider
further instructions from each from each of your professors/instructors from each of
your professor/instructors as to how will you accomplish the exercises whether
printed or be sent online.
4. Read and/or refer to other sources or references on related topics for additional
learning contents.
5. Optimize your time and effort to complete this hand out to achieve desired learning
outcomes for the semester.
6. Arrange with your course professor/instructor the schedule of submission of
exercises and/or requirements.
7. For this semester, there are only three face-to-face sessions. All students must attend
the schedules of Onboarding or Orientation day, Midterm Examination day and
Final Examination day. Further information will be given as to the dates and venues
of these face-to-face sessions.
8. All exercises in the handout will also serve as your attendance. Hence, schedule of
submissions must be agreed upon between the professor/instructor and students to
secure attendance.
9. For smooth and fast communication, maintain your active contact number. Do not
be changing your mobile numbers if not necessary.
10. Username of your social media accounts like Facebook and Messenger must be
your real complete name. No pseudonyms, no aliases, no codenames.
11. Secure contact details of all your course professors. Feel free to contact or confer
with your course instructor/professor for any concern, clarification about the
handout content.
12. Above all, your safety and health are our concern. Always maintain a minimum
health guideline provided by DOH and IATF. Wear facemask, bring your own
sanitizers, and maintain a 2-meter physical distancing.
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CONTENTS
Title Page Time
Frame
UNIT 1. INTRODUCTION TO GENETICS
2 weeks
Lesson 1.1 The History and Development of Genetics................... 1 1 week.
Lesson 1.2 Genes, DNA, and Chromosomes: An Intro to 24 1 week
Heredity.........................................................................
viii
RUBRIC FOR CHECKING ESSAY TYPE OF QUIZ IN SCIENCE
Weig Poi
3-
5-STELLAR 4-WELL 2-LIMITED 1-I NEED hted nts
CRITERIA MODERATE
(wow!) DONE (aaah.) (huh?) HELP! (huhu!) Value Ear
(hmm.)
ned
IDEAS The essay is The essay is The essay is The essay is The essay shows
-Controlling idea fully focused consistently sufficiently minimally little or no focus
-Supporting ideas and contains a focused and focused and focused. The and the ideas are
-Use of details wealth of ideas contains ample contains some provided unclear,
-Awareness of and examples. ideas and ideas and examples are irrelevant, or
purpose The writer uses examples. The examples. The vague or general repetitive. The X2
-Sense of scientific writer may use response is and the response response is
completeness reasoning to scientific generally demonstrates incomplete or too
addresses ideas reasoning to appropriate to minimal brief.
and arguments. addresses ideas the purpose. awareness.
and arguments.
ORGANIZATION The organization The organization The The organization The essay shows
-Introduction/body/ of ideas supports is appropriate organization is is formulaic or little evidence of
conclusion the writer’s and the generally inappropriate. organization or
-Sequence of ideas focus. Ideas are sequencing of appropriate and The response sequencing.
-Grouping of ideas grouped in a ideas is logical. the ideas are may lack a clear Transitions are
-Effective transitions logical manner. Varied clearly introduction or not used. The X1
-Awareness of purpose Effective and transitions are sequenced, but conclusion. response is
varied used. may be Transitions are incomplete or too
transitions are repetitive. rare. brief.
used. Transitions are
used
ix ix
STYLE The writer The language The language The language The language and
-Sentence variety utilizes carefully and tone of the and tone are and tone are tone are
-Word choice crafted phrases essay enhance appropriate. uneven. Word inappropriate.
-Audience to create a the persuasive Word choice is choice is simple, Word choice is
awareness sustained tone purpose. Word adequate, but ordinary, or incorrect or
-Personal voice and an choice is may be simple repetitive. confusing. The X1
authoritative appropriate. or ordinary. There is response is
voice. Word Sentences are Some sentence minimal incomplete or too
choice reflects varied. variety is variation in brief.
an advanced evident. sentence length
vocabulary. and structure.
CONVENTIONS The writer The writer The writer The writer The writer lacks
-Sentence formation demonstrates demonstrates demonstrates demonstrates understanding of
-Subject-verb full command of knowledge of sufficient minimal control the conventions
agreement the conventions the conventions control of the of the of written
-Standard word of written of written conventions of conventions of English. Errors
forms English English. Errors written written English. are pervasive. X1
-Punctuation, language. No are minor and do English. Errors Errors are The response is
spelling, and errors are not interfere may interfere frequent and incomplete or too
capitalization evident. with meaning. with meaning, interfere with brief.
but are not meaning.
distracting.
TOTAL 25
x
EducSci 323A Genetics
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Educ Sci 323A Genetics (Laboratory) is divided into two parts: The
first part is a laboratory activity on DNA. This is the coverage for midterm.
The second part is a laboratory activity on the Mendelian Genetics on fruit
flies. This is the coverage for the final term.
Course Description
This 1-unit course deals with wet laboratory activities on the nature of
genetic materials, and variation and pattern of inheritance using model
oraganisms.
Course Outline
Activity
No. Title of the Page
Experivment Number
Midterm
(Part I) The DNA
1 DNA Extraction on Fruits
Finals
(Part II) Mendelian Genetics in Fruitflies
2 Culturing D. melanogaster
3 Setting Up the Cross for D.
melanogaster
4 Genetic Crosses in D.
melanogaster
Course Requirement
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NOT FOR SALE.
EducSci 323A Genetics
Let’s start! 😊
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EducSci 323A Genetics
Unit 1
INTRODUCTION TO
GENETICS
2 WEEKS
Lesson 1.1
(1 week)
Lesson 1.2
(1 week)
1. Name global and local scientists who have great achievements in Genetics.
2. Sequence some major events in the past and present of Genetics.
3. Conclude the present and future impacts of a significant event in Genetics to
the scientific community and the society.
4. Create an essay as a response to the selected scientist (or group of
scientists).
Introduction
In Modern Genetics, one
important breakthrough is the
development of DNA sequencing.
With this, several molecular
genetic researches were published.
Some of its applications include
gene therapy, plant and animal
breeding, and the diagnosis of
infectious diseases.
Gregor Mendel
(The Father of Genetics)
LESSON PRE-TEST
What Do You Already Know?
1. 2. 3.
7.
6.
8. 9. 10.
GenBank database
Human DNA sequncing begins First animal gene cloned formed
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Check the correct answers found at the last page of the lesson.
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Self-Rating Journal
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LESSON PROPER
Let’s start our lesson. You have a suggested time allotment of 3 hours to
finish all the readings, activities, and assessments. That is only a
suggested time frame. You may answer all the activities at your most
convenient time. Do not forget to read all instructions. Happy reading! 😊
T
[Optional: To read more about the news, you A research group in China has
Y may check the URL link given in E-visit corner sequenced the genome of the COVID-
below (Science News). 19 virus and reported that the virus
most likely originated from bats.
Optional: To read the research article, you
may check the URL link given in E-visit corner Source: Asian Scientist Newsroom
(Research Article)]
Title of the Headline: Chinese Scientists Title of the Research article: Identification of a
Sequence Genome of COVID-19 novel coronavirus causing severe pneumonia in
GO TO: human: a descriptive study
https://www.asianscientist.com/2020/02/topn GO TO:
ews/china-coronavirus-covid-19-study/ https://journals.lww.com/cmj/FullText/2020/05050/Ide
ntification_of_a_novel_coronavirus_causing.3.aspx
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After reading the Science news, please answer the following questions:
A
N
A 2. Who are the group of scientists who sequenced the genome of the COVID-
L 19?
Y
S
I
S
3. What do you think are the roles of the past events or history of Genetics to the
recent achievement on the sequencing of the COVID-19 corona virus
genome?
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4. What do you think are the present impacts of the said achievement or
discovery to the Scientific community and the society? How about the future
impacts?
A
N
A
L
Y
S
I
S
Getting There...
The Science of Genetics has developed overtime—from the discovery of
genes and DNA to a more advanced sequencing of DNA. Major events from the
past such as the discovery of genes, DNA, and chromosomes had opened to a
flourishing advancement and promises of genetic engineering and DNA
sequencing.
Scientific discoveries and breakthroughs are influenced by the demand of
the society. An expamle is DNA sequencing. Then and now, many genomes of
important unicellular and multicelluar organisms were sequenced such as
humans, pathogenic bacteria like E. coli, and model organsims like fruit flies
and rats. These breakthroughs have helped the advancement in Medicine,
agriculture, environment, and other global demands.
The promise of DNA sequencing fed the society’s demand during the
COVID-19 pandemic. One of which is when the genome of the COVID-19
coronavirus was sequenced. This paves the way to undertanding the identity of
the virus and its source. In turn, this may serve as a baseline information to
studying its characteristics, diagnosis of the disease, and even the discovery of
vaccine and treatment.
Behind all achievements of Genetics are the great scientists of the past
and today. In this lesson, let us know some of these important people and their
achievements.
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After Mendel. ..
A fter Mendel
and after the first
isolation of DNA,
many great
achievements in Walther Flemming
Wilhelm Johannsen Thomas Hunt Morgan
Genetics (1879)
(1909) (1911)
followed. Some He is the first to
He coined the word He used fruit flies as a
of these are the describe the
gene to describe the model organism and
discovery of chromosome
Mendelian units of show that genes are the
gene, the behavior during units of heredity
heredity
structure of DNA, animal cell division
and DNA
A sequencing. Let’s
B recognize some
S notable scientists
T behind these great
R achievements.
[Photo start from
A
the upperleft; George Beadle and
C
clockwise (oldest Edward Tatum (1941)
T They affirm the “one
to latest)
I gene, one enzyme
O hypothesis”
N
DNA STRUCTURE
UNRAVELLED!
In 1953, Francis Crick and James
Frederick Sanger Watson unravelled the double helix
(1975-1977) structure of DNA.
Sanger and his Barbara McClintock
colleagues developed (1944)
the rapid DNA She discovered that genes
Joe Hin Tjio
sequencing methods. can jump around on
(1955)
This great achievement chromosomes showing
He defined 46 as
open up for the many that genome is more
the exact number
sequencing of human dynamic. These genes are
opportunities on the called “jumping genes.
chromosomes
genome of organisms.
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M any of our
Specialization: Genetics and Plant Breeding
Year Proclaimed as National Scientist: 1986
Filipino
He developed and improved varieties of rice
scientists and and corn, food legumes, fruits and ornamental
academicians plants. His research output and writings paved
are getting into the way for the launching of programs rainfed
the Dioscoro L. Umali
and upland agriculture, social forestry,
advancement of environmental conservation, and rural poverty
“Father of Philippine
Genetics. They alleviation. (source: Directory of NAST, 2006)
Plant Breeding”
are involved in
A the publication Specialization: Genetics and Plant Breeding
of scientific Year Proclaimed as National Scientist: 1994
B
researches,
S Provided leadership in the development,
promoting their isolation, and release of many rice cultivars in
T
goals and the Philippines. The classic rice cultivar C4.63
R advocacies to is high yielding, resistant to many diseases and
A the society, and insect pests and has become the standard for
C utilizing the Pedro B. Escuro high quality rice in the Philippines as well as in
T Science of many other rice growing countries. (source:
I Directory of NAST, 2006)
Genetics in
O solving some of Specialization: Biochemical Genetics
N our country’s Year Proclaimed as National Scientist: 1998
problems.
Let us recognize She pioneered cytogenetics of various Philippine
some of our crops and the biochemical genetics of macapuno.
She initiated researches in genome analysis and
remarkable molecular/biochemical markers in important
scholars who agricultural crops. (source: Directory of NAST,
Dolores A. Ramirez
have been 2006)
awarded as
National Specialization: Plant Breeding
Scientists! Year Proclaimed as National
Scientist: 2005
2.
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Headline 1:
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Headline 2:
Source:
b. Summary:
A
P
P
L c. Scientist or group of Scientists:
I
C
A d. What do you think is the present impact?
T
I
O
N
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1. Read the headlines from newspapers or Science news about the achievements of
some Filipino scientists or academicians on the following subjects:
2.
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Page 17 EducSci 323A Genetics
3.
A
P
4.
P
L
I
C
A
T
I
O
N
5.
Sum It Up!
1. Notable geneticists in the history. Gregor Mendel, the Father of Genetics turn
employ scientific approach to study the variation and inheritance in organisms.
Friedrich Meischer isolated the DNA for the first time. Joe Hin Tjio defined 46
as the exact number of human chromosomes. Walther Flemming was the first to
describe the chromosome behavior during animal cell division. Wilhelm
Johannsen coined the word gene to describe the Mendelian units of heredity.
Watson and Crick described the double helix DNA Barbara McClintock
discovered jumping genes. Thomas Hunt Morgan used fruit flies as a model
organism and show that genes are the units of heredity. George Beadle and
Edward Tatum affirm the “one gene, one enzyme hypothesis”. Sanger and his
colleagues developed the rapid DNA sequencing methods.
2. Local Filipino Scientists. Among our National Scientists are: Dioscoro L. Umali
(Father of Philippine Plant Breeding), Pedro B. Escuro, Dolores A. Ramirez, and
Ricardo M. Lantican. These National Scientists have greatly contributed on plant
breeding and enhancement of the quality and yield of important agricultural crops.
3. Timeline on the development of Genetics. The Science of Genetics started when
Mendel worked with pea in his garden. Many significant events followed: DNA
was isolated, the behavior and features of chromosomes were identified, DNA
sequencing was developed, and many important model and non-model organisms
were sequenced.
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LESSON POST-TEST
How Much Have You Learned?
How much have you learned from the previous readings and
activities? This time, we will have our evaluation. Read the directions
carefully. Good luck! 😊
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8. Thomas Hunt Morgan and his group studied the fruitfly Drosophila melanogaster
and showed that chromososmes carry genes. _______________
9. Francis Crick and James Watson describe the double helix model of DNA. ______
10. George Beadle and Edward Tatum, throug experiments on the red bread mold
Nerospora crassa, they showed that genes act by regulating distinct chemical
events- affirming the “one gene, one enzyme” hypothesis. _______________
2. In your own words, list in order at least 5 major significant events in the history of
Genetics. Then, add a recent trend in Genetics in the global or local scenes. You may
use examples from our previous activities based on what you have learned.)
2.
3.
4.
5.
Local Scene
Global scene
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Self-Reflect
Create an essay as a response to the selected scientist (or group of Scientists)
who have great achievements in Genetics. Write at least 3 to 5 paragraphs. Your
essay should cover but not limited on the following:
a. Name of the scientist and their significant achievements
b. Present and future impacts of the achievement to the scientific
community and the society
c. Your personal response as a Science student and future Science
educator
Essay:
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I hope you have learned a lot from the lesson. Please rate yourself
. by checking the following Learning Comptency cheklist. 😊
Self-Rating Journal
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Answer Key
LESSON PRE-TEST
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Introduction
LESSON PRE-TEST
What Do You Already Know?
2. Label the following structures below. Get your answers from the word box.
1.
2. 3.
4.
5.
Word Box:
Nucleus Chromosomes RNA Histone Proteins
Mitochondria DNA Nucleosomes Endosome
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3. Compare and contrast the sturcture of DNA and RNA based on their structure and
function.
3’ A T G G C A C T 5’
5’ 3’
Check the correct answers found at the last page of the lesson
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Self-Rating Journal
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Page 28 EducSci 323A Genetics
LESSON PROPER
Let’s start our lesson. You have a suggested time allotment of 5 hours to
finish all the readings, activities, and assessments. That is only a suggested
time frame. You may answer all the activities at your most convenient
time. Do not forget to read all instructions. Happy reading! 😊
Check the correct answers found at the last page of the lesson
😊
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Page 29 EducSci 323A Genetics
A
Things to do:
C
T 1. Choose a photo of a famous family. Paste your photo on the frame above.
I Optional: Take a family photo. Include your biological parents and your
V siblings.
I
T 2. Observe the picture keenly. Spot the similarities and differences (e.g., in
Y physical appearance and talents) among the family members—from parents to
the children, and between siblings.
Optional: You may talk with your parents and siblings about your similarities
and differences.
Child With the mother With the father With the siblings
Similarities
Differences
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1. Based from your observation, what physical characteristics does the child have
in common with her/his parents? With the siblings? What makes her/him
unique from the rest of the family?
Optional: (What do you have in common with your parents? With your
siblings? What makes you unique from the rest of the family members? )
A
N
2. What do you think, accounts for family resemblance? Write words or
A
phrases as many as you can the probable reasons for family resemblance. Write
L
on the oval below. Also, write the probable reasons for the differences on the
Y
rectangle below.
S
I
S
Getting There...
You have just listed words or phrases the probable reasons on the
resemblance and differences of physical appearance among family
members.What you just did earlier is the quest in Genetics. Genetics is the
scientific study of heredity and variation in living organisms, including humans.
Heredity is the transmission of traits from one generation to the next. Variation
is demonstrated by the differences in appearance that offspring show from parents
and siblings. In a literal sense, children do not inherit particular physical traits
from their parents. It is genes that are actually inherited.
Genes are the units of heredity, and are made up of segments of DNA. Genes
are passed to the next generation through reproductive cells called gametes
(sperm and eggs). Each gene has a specific location called a locus on a certain
chromosome. Most DNA is packaged into chromosomes. One set of
chromosomes is inherited from each parent. These molecules of heredity-- the
genes, DNA, and chromosomes, are what we are going to tackle in this lesson.
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Figure 1.2. The level of structural organization of gene, DNA, and Chromosomes based
on their locations.
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Nucleic acids are one of the types of biomolecules or biopolymers that have
roles in the transmission of hereditary information. Two kinds of nucleic acids are
found in cells: ribonucleic acid (RNA) and deoxyribonucleic acid (DNA). As a
biopolymer, nucleic acid is made up of a repetitive subunit of monomers called
nucleotide. The nucleotide is composed of different subunits: the nitrogenous base
[Adenine, Thymine in (or Uracil in RNA), Cytosine, Guanine], the sugar, and the
A phosphate.
B
S DNA
T
R Deoxyribonucleic acid, or DNA is a type of
A nucleic acid which is a double helix chain of
C molecules. It has a segment of heritable
T factors called genes that determines the
I unique external and internal characteristics
O of an organism. Hence its popular identity
N phrase, “the blueprint of life”. DNA is
present in the chromosomes of the nuclei of
eukaryotic cells (Figure 1.3). DNA is also
present in prokaryotic cells and virus. James Figure 1.3 Location of DNA in
eukaryotic cells. DNA is strung and
Watson and Francis Crick co-originated the packaged in the chromosomes of the
double helix molecule of DNA. nucleus in eukaryotic cells.
E-Visit Corner
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Nucleotides
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Page 35 EducSci 323A Genetics
A-T pairs linked with 2 hydrogen bonds C-G pairs linked with 3 hydrogen bonds
A
B
S Sample complementary base-pairing:
T DNA RNA
R
5’ AATTTGCGTATGCGTGACGTG 3’ 5’ AGCGAUAGCUAGCUGGCAGC 3’
A 3’ UCGCUAUCGAUCGACCGUCG 5’
3’ TTAAACGCATACGCACTGCAC 5’
C
T
I B. Sugars
O
N Both types of sugar of each nucleic acid is a A
pentose. The sugar component of RNA is D-ribose.
In DNA, it is 2-deoxy-D-ribose. The full name of
ẞ-D-ribose is ẞ -D-ribofuranose and that of ẞ -2-
deoxy-D-ribose is ẞ -2-deoxy-D-ribofuranose.
B
C. Phosphates
Phosphate is an anion, salt, functional group or
ester derived from a phosphoric acid. The third
component of nucleic acids is phosphoric acid. When
this group forms a phosphate ester bond with a
nucleoside (base-sugar), the result is a compound Figure 1.9 Sugars of
(A) DNA; and (B)
known as a nucleotide.
RNA
Figure 1. Structure of
phosphate group in a
nucleic acid
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1. Draw a simplified structure of DNA showing the base, sugar, and phosphate
group. Color your nitrogenous bases: (Adenine= blue, Thymine= red;
A Cytosine= orange, Guanine= green
B
S
T
R
A
C
T
I 2. Make a venn diagram to compare and contrast the structure and function of
O DNA and RNA.
N
DNA RNA
Function:
Function:
Structure:
Sugar: Sugar:
Base: Base:
Function:
Location:
Location:
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a. DNA sequence
3’ A C G T C G G C C T A C G 5’
5’ 3’
b. RNA sequence
A 3’ C G C G A U A C G U C A G 5’
B 5’ 3’
S
T
R
A
C Check the correct answers found at the last page of the lesson
T
I
O Thank you for answering! 😊
N
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E-Visit Corner
TOPIC: Chromosomes
YOU MAY VISIT:
https://www.youtube.co
Figure 1.13 End part of the chromosome. m/watch?v=IePMXxQ-
Telomeres are in color red. KWY
Photo Credit: NCI Center for Cancer Research
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A B
Chromosome Organization
A
B
Figure 1.15 Organization in chromosomes. A) Loosening the condensed
S chromosomes displays proteins like histones and nucleosomes. Some proteins like
T histones wrap the DNA. B) Chromosome proteins are further coiled. C-D)
R Supercoiled proteins results to a thread-like fiber chromatin: Extended chromatin
A (C); and a more condensed chromatin (D) A compacted condensed chromosome
C resulted after many replications of DNA.
T
I Chromosome Carries a lot of
O genetic information
N
Controls inherited
character of the
organism
Figure 1. Chromosomes carrying genes.
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Types of Chromososmes
X- X-shaped
Chromosome chromosome
Based on Shapes
Y- Y-shaped
Chromosome chromosome;
Photo credit:
determine the male https://www.pinterest.ph/
sex on the 23rd
chromosome (XY)
centromere approximately in
Metacentric
the middle, such that the two
Based on arms are of similar length
Centromere
Position Submetacentric centromere between one end
and the middle, thus having a
long arm, and a short arm
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A
2. Draw the structure of the following types of chromosomes:
B
S
a. Sister Chromatids b. Homologous chromosomes c. Acrocentric
T Chromosome
R
A
C
T
I
O
N
1.
2.
3.
4.
5.
Check the correct answers found at the last page of the lesson
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1. At home, pick two different species of the same family. Capture images of both
species (e.g., dogs). Put the images on the boxes below.
A
P
P
L
I
C
A
T
I Species A: ______________________ Species B: ____________________
O
N 2. List at least three (3) physical characteristics that make these two different
species different from each other (e.g., eye color)
3. Pick at least one (1) physical trait (e.g., eye color). Assign a gene name of the
physical trait on each species—for example, Gene A for Species A; Gene B for
Species B.
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A
P
P
L
I Chromosome of Species A Chromosome of Species B
C
A
5. Loosen your chromosome. Draw the DNA on your chromosome showing the
T
complementary nitrogenous bases
I
O
N
6. Encircle a segment in the DNA as your hypothetical gene. Write the sequence
of the nitrogenous bases of DNA on the box below. Do not forget to write the
complementary bases.
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Analysis:
A
P
P 2. What do you think is the relationship between the gene, DNA, and
L chromosomes?
I
C
A
T
I
O
N
3. In your own words, compare and contrast the gene, DNA, and chromosomes.
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Sum It Up!
Genes are the segment of DNA which is the unit of heredity.
Deoxyribonucleic acid or DNA is a type of nucleic acid which stores genetic
information. It consists of a repetitive unit of monomers called nucleotides.
Nucleotides are the building blocks of DNA which are composed of sugar,
nitrogenous base (Adenine, Thymine, Cytosine, Guanine), and phosphate group.
Ribonucleic acid or RNA is another type of nucleic acid consist of repetitive units
of nucleotides. It plays a major role in the synthesis of proteins
DNA and RNA differ in structure and function. DNA is a double helix molecule,
while RNA is a single stranded molecule. DNA has a deoxyribose sugar while RNA
has a ribose sugar. DNA has nitrogenous bases of Adenine (A), Thymine (T),
Cytosine (C), and Guanine (G), while in RNA, although it also has the A, C, G, the
thymine is replaced by Uracil. In terms of their function, DNA plays a major role
in storing genetic information. it is where the gene, the unit of heredity, are found;
while RNA plays a major role in the synthesis of proteins.
Both DNA and RNA nitrogenous bases has rules in complementary base pairing:
Adenine always pairs with Thymine (or Uracil in RNA), and Cytosine always pairs
with Guanine. Pyrimidine (C, T) always pairs with purine (A, G).
Chromosomes are structures found in the cell’s nucleus. It is a condensed form of
a thread-like structure which houses DNA and proteins like histones and
nucleosomes.
Genes, DNA, and RNA are important molecules of heredity. Genes, the unit of
heredity, are segments of DNA. DNA stores genetic information which can be
found in the chromosomes.
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Direction: Write the letter of the correct answer. If you want to change your
answer, please mark X the previous answer and change it with the final answer.
Then, write your explanation for your answer. Points will not be valid if there is no
explanation. (2 points in each item number)
1. Which of the follwing best defines deoxyribonucleic acid (DNA)?
A. DNA is a segment of gene.
B. All segments of DNA contains expressed genes.
C. DNA is a type of nucleic acid containing nucleotides arranged in a wavy,
single strand
D. DNA molecule is composed of two long chains of nucleotides arranged in a
double helix.
Answer:
Explanation:
2. What do you call the “building blocks” of both DNA and RNA?
A. nitrogenous bases
B. nucleotides
C. genes
D. amino acids
Answer:
Explanation:
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Answer:
Explanation:
Answer:
Explanation:
Answer:
Explanation:
6. All of the following nitrogenous bases are found in DNA EXCEPT ________.
A. thymine
B. adenine
C. guanine
D. uracil
Answer:
Explanation:
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Answer:
Explanation:
Answer:
Explanation:
Answer:
Explanation:
Answer:
Explanation:
11. What would be the complementary strand if the sequence of bases in one strand
of DNA molecule is 3'TAACGT5'?
A. 3'UAACGU5'
B. 5'UAACGU3'
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C. 5'ATTGCA3'
D. 3'ATTGCA5”
Answer:
Explanation:
Answer:
Explanation:
13. How do the two members of a pair of homologous chromosomes differ from
each other?
A. the precise sequence of the DNA within each of the chromosomes
B. the centromere position of each chromosome
C. the relative position of the genes present on each of the chromosomes
D. the staining patterns of each chromosome
Answer:
Explanation:
Answer:
Explanation:
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Answer:
Explanation:
2. In your own words, illustrate and explain the relationship between the gene,
DNA, and chromosomes.
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Self-Reflect
1. Recall and reflect on the structure and fuction of the molecules of heredity—the
genes, DNA, and chromosomes. Then, write an appreciation letter to your DNA.
Relate it to the structure and function of the genes, and chromosomes. Write 3 to
5 paragraphs.
Appreciation Letter:
Date: _________________
Dear DNA,
_____________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
____________________________________________________________________
___________________________________________________________________
Sincerely Yours,
___________________________________
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.
Please rate yourself by checking the following Learning
Comptency cheklist. 😊
Self-Rating Journal
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Page 53 EducSci 323A Genetics
Answer Key
LESSON PRE-TEST
1) Genes are the segment of DNA in an organism. It is the unit of heredity.
It predetermines the character traits of the offspring.
2) Labelling:
1. Nucleus 2. Chromosomes 3. DNA 4. Histone proteins 5. Nucleosomes
3) 5’ T A C C G T G A 3’
LET’S PRACTICE YOUR VOCABULARY
1. CENTROMERE 6. HOMOLOGOUS CHROMOSOMES
2. CHROMOSOME 7. NUCLEIC ACIDS
3. DEOXYRIBONUCLEIC ACID 8. RIBONUCLEIC ACIDS
4. DEOXYRIBOSE 9. RIBOSE
5. GENES 10. SISTER CHROMATID
1.
Adenine p
Phosphate
group
Nitrogenous
base Deoxyribose
sugar
A nucleotide
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2. RNA
DNA
3.
a 5’ T G C A G C C G G A T G C 3’
b. 5’ G C G C U A U G C A G U C 3’
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2
MEOSIS AND SEXUAL
Unit
LIFECYCLES
1 week
Introduction
T he exact number of
chromosomes in an organism is crucial to
maintain and continue its existence. In
humans, the number of chromosomes is 46
(that is, 23 pairs). The first 22 pairs are body
chromosomes (also called autosomes) from
body cells (also called somatic cells) except
sex cells. The 23rd chromosomes are the sex
chromosomes from sex cells-- the egg and
sperm cells (also called gametes). The
excess or lacking number of chromosomes
results in a genetic disease; an example is
Figure 2.1 Couple with downsyndrome
Down Syndrome in humans having an extra
celebrate 22 years of Happy marriage
number of chromosomes (Figure 2.1)
The union of the sperm and egg cell Source: People.com
results to a diploid zygote having 46
chromosomes carrying genes from the chromosomes before the union—a term
mother and father. This zygote undergoes called haploid. There is a special type of
several body cell divisions to grow, cell division which produces haploid sex
differentiate, and develop into a full-grown cells. This process is called meiosis.
human in a process called mitosis. Since the How these sex cells become haploid to
human zygote is diploid, both sperm cells maintain the number of the exact
and egg cells should have half of its chromosomes in an offspring is the
number or having a single set of pair of subject in this lesson.
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LESSON PRE-TEST
What Do You Already Know?
What do you already know about Meiosis? Before going
through the lesson, please check your background by answering the
following activity. Do not sneak for an answer yet. You may check
the correct answers only after you have answered all questions.
Correct answers can be found at the last page of the lesson. Don’t
forget to read the direction. 😊
A. True or False. Write TRUE if the statement is correct, and write FALSE if the
statement is incorrect then write the correct answer.
1. After the complete process of meiosis, this results to four diploid daughter cells.
2. One of the uniqueness of meiosis that is not in mitosis, is that meiosis produces
gametes.
3. Meiosis and mitosis both undego cytokinesis.
4. Crossing over occurs during the Prophase II stage of Meiosis.
5. Crossing over is the exchange of chromosome segments between non-sister
chromatids.
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MEIOSIS II
Explanation
Meiosis II:
1.
2.
3.
4.
Check the correct answers found at the last page of the chapter
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Self-Rating Journal
LESSON PROPER
Let’s start our lesson. You have a suggested time allotment of 2 1/2
hours
LET’StoPRACTICE
finish all the readings,
YOUR activities, and assessments. That is
VOCABULARY!
only a suggested time frame. You may answer all the activities at
your most convenient
Direction: time.
I have here keyDo not forget
words for ourtolesson.
read all instructions.
Fill the missing letters to complete
the correct word. Happy reading! 😊
Check the correct answers found at the last page of the lesson
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This handout
Check the is intended
correctonly for the
answers use ofatstudents
found the last who
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of the lessoncourse.
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Page 61 EducSci 323A Genetics
L
LET’S GET STARTED!
A
C 1. Paste the family photo of the previous activity from the last lesson (in Lesson
T 1.2)
I 2. List at least 1 obvious physical trait the child inherits from the Mother and 1
V obvious physical trait the child inherits from the father.
I
Physical trait inherited from Mother: ________________________
T
Y Physical trait inherited from Father: __________________________
3. There are two homologous chromosomes (long and short) in the circle below.
Color one of the chromosomes in a homologous chromosome pair as red
(from Mother) the other chromosome, blue (from father). Do the same in the
short homologous chromosomes.
In a blue long chromosome, put a stain or segment for the gene of a physical
trait inherited from Father. Label it. In a red short chromosome, put a stain or
mark for the gene of a physical trait inherited from Mother. Label it.
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Page 62 EducSci 323A Genetics
4. Consider the circle (where the chromosomes are located) as a sex cell. (Put your
gene mark in the chromosome in each division).
On your own, conclude the results after some divisions of the sex cell by asnwering
the following:
a. Separate all homologous chromosomes into sister chromatids. In one cell, draw
and color the long short sister chromatids. Do the same on the other cell.
A
C
T
I
V
I b. Paste the result above on the circles below. Separate the sister chromatids
T into individual chromatids. Each cell should compose one long chromatid
Y and one short chromatid.
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1. During the process of the cell division, what happened to your gene
segments in the chromosome?
2. During the process of the cell division, what happened to the homologous
A chromosomes? the sister chromatids?
N
A
L
Y
S
I
S
3. How does the diploid cell reduced into haploid?
Getting There...
Sex cells (or gametes) such as sperm cell and egg cell should be in
haploid form, so that after the union of these cells, the exact number of dipliod
chromsome of the offspring will be maintained. To reduce the sex cells into
haploid form, it should undergo a series of special type of cell division. This
special type of cell division that reduces the sex cell into haploid cell is called
Meiosis.
What you have just did in the previous activity is an overview on how
the sex cells divide and how the chromosomes behave during Meiosis. In the
next section, let’s dig deeper the process of Meiosis.
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Overview of Meiosis
LET’S GET TO KNOW MORE!
Meiosis is a type of cell division
wherein the number of chromosome
sets is reduced from diploid to haploid.
It has two stages of cell division: (1)
Meiosis I and Meiosis (II). In the first
A cell division (meiosis I), homologous
B chromosomes separate. It results in two
S haploid daughter cells with replicated
T chromosomes; it is called the
R reductional division. In the second
A cell division (meiosis II), sister
C chromatids separate. It results in four
T haploid daughter cells with
I unreplicated chromosomes; it is called
O the equational division. (Figure 2.1)
N
Meiosis I is preceded by interphase, in
which chromosomes are replicated to
Overview
form sister of chromatids.
Meiosis The sister
chromatids are genetically identical and
joined atMeiosis is a type (Figure
the centromere. of cell division
2.1) Photo Credit: 2008 Pearson Education, Inc., publishing
wherein the number of chromosome sets is
as Pearson Benjamin Cummings
reduced from diploid to haploid. It has two
Figure 2.1. General Overview of the
stages of cell division: (1) Meiosis I and
behavior of chromosomes during Meiosis
Meiosis (II). In the first cell division (meiosis
Photo Credit: 2008 Pearson Education, Inc., publishing
Overview of Stages
I), homologous of Meiosis:separate.ToItremember
chromosomes Figure 2.1.
the stages
as Pearson ofGeneral
Benjaminmeiosis Overview
easily,
Cummings of the
use an acronym.
results in two haploid daughter cells with (e.g., PMAT)
behavior of chromosomes during Meiosis
replicatedI chromosomes;
Meiosis it is II
Meiosis called the
reductional division. In the second cell
Prophase
division I
(meiosis Prophase
II), sister II
chromatids E-Visit Corner
separate. It results in four haploid daughter To remember the stages of meiosis easily, use an acronym.
Metaphase I Metaphase (e.g.,
II TOPIC: Meiosis
cells with unreplicated chromosomes; it is PMAT)
Anaphase
called I
the equational Anaphase
division. (Figure 1)II GO TO:
https://www.youtube.c
Telophase I Telophase II om/watch?v=qCLmR9-
YY7o
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Stages of Meiosis
Meiosis I
In the first cell division (meiosis I), homologous chromosomes
separate. It results in two haploid daughter cells with replicated
chromosomes; it is called the reductional division.
A
B
S
T
R
A
C Photo Credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Figure 2.2. The stages of Meiosis I.
T
I Prophase I Prophase I typically occupy more than 90% of the time required for
meiosis. In this stage, chromosomes begin to condense. Other important
O
events during Prophase I includes synapsis and crossing over. In
N
synapsis, homologous chromosomes loosely pair up, aligned gene by
gene. In crossing over, nonsister chromatids exchange DNA segments.
Each pair of chromosomes forms a tetrad, a group of four chromatids.
Each tetrad usually has one or more chiasmata, X-shaped regions where
crossing over occurred.
Metaphase Tetrads line up at the metaphase plate, with one chromosome facing
I each pole. Microtubules from one pole are attached to the kinetochore
of one chromosome of each tetrad. Microtubules from the other pole are
attached to the kinetochore of the other chromosome
Anaphase Pairs of homologous chromosomes separate. One chromosome moves
I toward each pole, guided by the spindle apparatus. Sister chromatids
remain attached at the centromere and move as one unit toward the pole
Telophase In the beginning of telophase I, each half of the cell has a haploid set of
I chromosomes; each chromosome still consists of two sister chromatids
Cytokinesis Cytokinesis usually occurs simultaneously, forming two haploid
daughter cells. In animal cells, a cleavage furrow forms; in plant cells, a
cell plate forms.
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A
B
S
T
R
A
C
T
I
O
Photo Credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
N
Figure 2.3 Stages of Meiosis II
Meiosis and mitosis are types of cell division. Meiosis occurs in sex cells (or
gametes). The process is important to maintain the number of chromosomes in
offsprings, necessary for the continuity of life. Mitosis occurs in all types of body cells
(or somatic cells). The process is improtant for growth, development, and repair.
A
B
S
T
R
A
C
T
I
O
N Photo Credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Figure 2.4 Difference between Meisosis and Mitosis
Table 1. Differences between meiosis and mitosis.
Property Mitosis Meiosis
DNA replication Occurs during interphase Occurs during interphase before
before mitosis begins meiosis I begins
Number of divisions One Two
Occurs during prophase I along with
Synapsis of Does not occur crossing over between nonsister
homologous chromatids; resulting chiasmata hold
chromosomes pairs together due to sister chromatid
cohesion
Number of Two, each diploid (2n) and Four, each haploid (n), containing half
daughter cells genetically identical to the as many chromosomes as the parent
and genetic parent cell cell; genetically different from the
composition parent cell and from each other
Enables multicellular adult to Produces gametes; reduces number of
Role in the arise from zygote; produces chromosomes by half and introduces
animal body cells for growth, repair, and, genetic variability among the gametes
in some species, asexual
reproduction
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Was everything clear to you? You may go back to the last section
if there are some concepts that are not yet clear. Take note of some
important facts and ideas. You may visit the E-reading corners for
supplemental readings. If you’re ready, please do the the following
activity.
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Page 69 EducSci 323A Genetics
Sum It Up
Meiosis is a special type of cell division the produces sex cells (or
gametes) with a haploid set of chromosomes.
There are two stages of Meiosis: Meiosis I and Meiosis II.
Meiosis I has 4 stages:
o PROPHASE I- Chromosome begins to condense; synapsis and
crossing over occurs; Each pair of chromosomes form a tetrad
o METAPHASE I- tetrad line up at the metaphase plate
o ANAPHASE I- Pairs of homologous chromosomes separate toward
each pole
o TELOPHASE I- sister chromatids are in the opposite poles; each
chromosome still consists of sister chromatids
MEIOSIS II has 4 stages:
o PROPHASE II- spindle apparatus form; sister chromatids move
towards the metaphase plate
o METAPHASE II- sister chromatids are arranged at the metaphase
plate
o ANAPHASE II- Sister chromatids separate
o TELOPHASE II- Chromosome are at opposite poles. Cells contain
haploid sets of chromosomes.
In terms of function, mitosis and meiosis have differences. Mitosis is
involved in the growth and renewal of cells. It occurs in somatic cells (or
body cells). It produces identical cells. In humans, it produces cells with a
diploid sets of chromosomes. Meiosis is a special type of cell division that
produces sex cells. It produces cells with a haploid set of chromosomes.
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LESSON POST-TEST
How Much Have You Learned?
How much have you learned from the previous readings
and activities? This time, we will have our evaluation. Read the
directions carefully. Good luck! 😊
I. Multiple Choice
Direction: Write the letter of the correct answer. Provide an explanation. Point
are not valid without an explanation. (2 points)
Answer:
Explanation:
Answer:
Explanation:
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3. Which of the following best states wherein Mitosis and Meiosis share in
common?
A. Number of divisions
B. Synapsis of homologous chromosomes
C. Number of daughter cells
D. Both undergo cytokinesis
Answer:
Explanation:
5. You view a meitoc cell in a light microscope. You saw tetrads lined up at the
center of the cell. What stage of meiosis it is?
A. Propahase I
B. Metaphase I
C. Metaphase II
D. Anapahase I
Answer:
Explanation:
II. Direction: Refer to the drawings in the figure below of a single pair of
homologous chromosomes as they might appear during various stages of either
mitosis or meiosis. Answer the following questions. Provide an explanation. (2
points)
A B C
.
D E F
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Self-Reflect
1. Read a Science news on Down Syndrome. Explain on your own what might have
caused the extra chromosomes. Reflect on yourself the importance of Meiosis in
your life. Write 2 to 3 paragraphs.
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I hope you learned a lot from the lesson. Please rate yourself by
checking the following Learning Comptency cheklist. 😊
Self-Rating Journal
______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
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Answer Key
LESSON PRE-TEST
A. TRUE OR FALSE
1. FALSE. Four haploid cells
2. TRUE
3. TRUE
4. FALSE- Prophase I
5. TRUE
B.
MEIOSIS I
MEIOSIS II
1. PROPHASE II- spindle apparatus form; sister chromatids move towards the
metaphase plate
2. METAPHASE II- sister chromatids are arranged at the metaphase plate
3. ANAPHASE II- Sister chromatids separate
4. TELOPHASE II- Chromosome are at opposite poles. Cells contain haploid sets
of chromosomes.
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Page 75 EducSci 323A Genetics
Introduction
LESSON PRE-TEST
What Do You Already Know?
6.
1. Humans Rats
______________ _______________
2. 7.
Fungi Fern
______________ _______________
8.
3. Protists Monkey
______________ _______________
Most Plants 9.
4. Hippopotam
______________ us _______________
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B. Sketch the life cycle of the following sexually reproducing orgasmisms: (Drawing
of organism is not necessary). Explain briefly.
a. Animals
Description
b. Fungi
Description
c. Plants
Description
Check the correct answers found at the last page of the chapter
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LESSON PROPER
Let’s start our lesson. You have 2 hours to finish all the readings,
actitivities, and assessments of the lesson. Please read all
directions carefully.
2. __IP__OID having a pair of each type of chromosome, one of the pair being
derived from the ovum and the other from the spermatozoon.
3. D__PLONT__C having a life cycle in which the main form, except for the
gametes, is diploid.
V
O 4. __ER__IL__ZA__ION a union or joining of two haploid gametes.
C
A 5. G__ME__E__ a reproductive cell having only half of a complete set of
B chromosomes
U
6. __AME__OP__YTE a plant (or the haploid phase in its lifecycle) which
L
produces gametes by mitosis in order to produce a zygote
A
R 7. HA__LOI__ having a single set of unpaired chromosomes
Y
8. HA__LON__IC having a life cycle in which the main form is haploid, with a
diploid zygote being formed only briefly.
11. SP__R__P__YT__ A plant (or the diploid phase in its life cycle) which
produces spores by meiosis in order to produce gametophytes
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1. What do you think is the young plant or seedling you’ve collected, a haploid
or a diploid organism? Why did you say so? How about the adult plant?
A
N
A
L
Y
S 2. What do you think is the young animal you have choosen, a haploid
I organism or a diploid organism? Why did you say so? How about the adult
animal?
S
Getting There...
Sexually reproducing organisms like plants and animals have have haploid
and diploid stages in its life cycle. The seedling or young plant and the adult plant
you’ve chosen are in diploid stages in its lifecycle; so they are diploid organisms.
The young and adult animals you’ve chosen are in diploid stages in its lifecycle;
so they are diploid organisms too.
To continue life, the diploid type of chromosomes in these organsisms
should be reduced by half through meisosis to produce gametes—which is the
haploid stage of the lifecycle of an organasism. Gametes should be in haploid form
so that during fertilization (or union of gametes), the exact number of
chromosomes will be maintained.
However, each type of sexually reproducing organism has a different
timing of haploid and diploid stages as well as the timing of alteration of meiosis
and fertilization. Let’s get to know more!
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Example: Most animals, including humans, have a diplontic sexual life cycle.
Cells that spend the majority of their lives in a haploid phase are considered to
have a haplontic sexual life cycle. In fact, organisms that have a haplontic life cycle
are only composed of a diploid cell when they are zygotes. Just like in the diplontic
life cycle, a haploid gamete from a female and a haploid gamete from a male will fuse
to make a diploid zygote. However, that is the only diploid cell in the entire haplontic
life cycle.
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The zygote undergoes meiosis at its first division to create daughter cells that
have half the number of chromosomes compared to the zygote. After that division,
all of the now haploid cells in the organism undergo mitosis in future cell divisions
to create more haploid cells. This continues on for the organism's entire life cycle.
When it is time to sexually reproduce, the gametes are already haploid and can just
fuse with another organism's haploid gamete to form the zygote of the offspring.
C. Alternation of Generation
A
B The final type of sexual life cycle is a kind of mix of the two previous
S types. Called alternation of generations, the organism spends about half of its
T life in a haplontic life cycle and the other half of its life in a diplontic life cycle.
R Like the haplontic and diplontic life cycles, organisms that have an alternation
A of generations sexual life cycle begin life as a diploid zygote formed from the
C fusion of haploid gametes from a male and a female.
T
The zygote can then either undergo mitosis and enter its diploid phase,
I
or perform meiosis and become haploid cells. The resulting diploid cells are
O
called sporophytes and the haploid cells are called gametophytes. The cells
N
will continue to do mitosis and split in whichever phase they enter and create
more cells for growth and repair. Gametophytes can then once again fuse to
become a diploid zygote of the offspring.
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A
B
S
T
R
A
C
T
I
O
N Figure 2.1. Sexual Life Cycle in Animals.
Photo credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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A
B
S
T
R
A
C
T
I
O
N
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A
B
S
T
R
A
C
T
I
O
N
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A
B
S
T
R
A
C
T
I
O
N
Figure 2.4. Sexual Life Cycle in Most Fungi and Some Protists
Photo credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Explanation:
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Sample
Collected
2
Scientific Name:
Common Name:
A
P
P Sketch of a Life Cycle (haplontic):
L
I
C
A
T
I
O
N
Explanation
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Sample
Collected
3
Scientific Name:
Common Name:
Explanation:
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Sum It Up!
Sexually reproducing organisms like animals, some plants, and fungi,
have different types of sexual lifecycle.
The type of sexual life cycle depends on the timing of haploid and
diploid generations
The types of sexual life cycles are: diplontic, haplontic, and alternation
of generation
Diplontic lifecycle occurs in organisms that spend most of its life’s
phase as diploid. For example, in animals such as humans.
Haplontic life cycle occurs in organisms that spend most of its life’s
phase as haploid. For example, in fungi and most protists
Alternation of generations occur in organisms that have life’s phase
alternation of being diploid and haploid. For example, in most plants.
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A. I, IV, and V
B. I, II, and IV
C. II, III, and IV
D. II, IV, and V
Answer: _____
Explanation:
2. Referring to a plant sexual life cycle, which of the following terms describes
the process that leads directly to the formation of gametes?
A. sporophyte meiosis
B. gametophyte mitosis
C. gametophyte meiosis
D. sporophyte mitosis
Answer: _____
Explanation:
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4. How does the sexual life cycle increase the genetic variation in a species?
A. by mitosis
B. by alternation of generation
C. by allowing crossing over
D. Both B and C
7. In comparing the typical life cycles of plants and animals, a stage found in plants but
not in animals is a
A. gamete.
B. zygote.
C. multicellular diploid.
D. multicellular haploid
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Refer to the life cycles illustrated in the figure below to answer the following questions:
Answer: _____
Explanation:
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9. Which of the life cycles is typical for plants and some algae?
A. I only
B. II only
C. III only
D. I and II
Answer: _____
Explanation:
10. Which of the life cycles is typical for most fungi and some protists?
A. I only
B. II only
C. III only
D. I and II
Answer: _____
Explanation:
Self-Reflect
Create a reflective essay on your own biologial life cycle. Your essay should
cover, but not limited, to the following:
1. Fertilization
2. You as a zygote at diploid stage
3. You as an adult at diploid stage
4. How you produced haploid sex cells
5. The type of your biological life cycle
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I hope you learned a lot from the lesson. Please rate yourself
by checking the following Learning Comptency cheklist. 😊
Self-Rating Journal
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
_______________________________________________________________________________________
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Answer Key
LESSON PRE-TEST
A.
1. Diplontic
2. Haplontic
3. Haplontic
4. Alternation of Generations
5. Diplontic
6. Diplontic
7. Alternation of Generation
8. Diplontic
9. Diplontic
10. Diplontic
B.
1. Lifecycle of Animals
Description
Animals have diplontic life cycle, of which, majority of its life (or adult
phase) is spent in diploid stage. Meoisis occurs during the diploid stage.
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2. Lifecycle of Fungi
Description
Most fungi have haplontic stage. Majority of its life is in haploid stage.
The adult (called gametophyte) are in haploid form. Meiosis occurs in
zygote which is a diploid.
3. Lifecycle of Plants
Description
Most plants undergo alternation of generation. Most of its phase are in diploid and
haploid form.
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1. ALTERNATION OF GENERATION
2. DIPLOID
3. DIPLONTIC
4. FERTILIZATION
5. GAMETES
6. GAMETOPHYTE
7. HAPLOID
8. HAPLONTIC
9. LIFECYCLE
10. SPORE
11. SPOROPHYTE
12. ZYGOTE
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Unit 3
MENDELIAN GENETICS
Lesson 3.1
Mendel’s Law of
Inheritance
Lesson 3.2
Punnett Square:
Monohybrid and
Dihybrid Cross
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1 week
Introduction
T he differences among organisms (variation) and how the character traits are
passed on from parents to offspring (inheriatance) had long been observed and discussed
before Genetics was established as a science. It is Gregor Mendel, the father of Genetics,
who turn the quest of inheritance and variation into science when he worked with pea
plants in his garden.
In this lesson, we will describe how Mendel did a scientific approach to identify
the laws of ineritance and how he was able to identify an important heritable factor that
is passed on from parents to offspring. This heritable factor is what we call now gene—
the unit of heredity.
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LESSON PRE-TEST
4. What was the most significant conclusion that Gregor Mendel drew from his
experiments with pea plants?
A. There is considerable genetic variation in garden peas.
B. Traits are inherited in discrete units, and are not the results of "blending."
C. Recessive genes occur more frequently in the F1 than do dominant ones.
D. Genes are composed of DNA.
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Check the correct answers found at the last page of the lesson
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LESSON PROPER
Let’s start our lesson. You have a suggested time allotment of 3 hours
to finish all the readings and assessments. That is only a suggested
time frame. You may answer all the activities at your most convenient
time. Do not forget to read all instructions. Happy reading! 😊
Direction: I have here key terms for our lesson. Fill the missing letters to complete
the
correct word.
6. H__M__ __YG__US both copies of a given gene have the same allele
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Mendel’s Experiment
Gregor Mendel, an Austrian monk
and a Botany teacher, did an experiment
with his pea in his garden that made a great
breakthrough in the history of Science.
The fundamental question on the variation
among organisms and how the traits are
A
B passed on from parents to its offspring was
S answered through Mendel’s experiment on Figure 3.1.2. Gregor Johan
the pea plant in his garden. This was the Mendel
Photo Credit: Britannica.com
T
R fundamental science of Genetics.
A
C
T Mendel’s Technique
I
O Mendel used the garden pea
N plant in his experiment because of the
following advantages: there are many
varieties with distinguishable features,
mating of plants can be controlled, each
pea plant has both sperm-producing
(stamen) and ovary-producing (carpel)
organs and pea plants can be cross-
polliated from each other.
Mendel cross-pollinate one
variety of pea to another by brushing
off the stamen of one variety of pea Figure 3.1.3. Mendel’s
plant (e.g., white folwer) and put in the Technique
Photo Credit: 2008 Pearson Education, Inc.,
publishing as Pearson Benjamin Cummings
carpel of another variety of pea plant
(purple flower of a pea plant).
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A
B
S
T
R
A
C
T
I
O Figure 3.1.4. Cross-pollination and self-pollination of pea plant by Mendel
N Photo Credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Mendel cross pollinated the true breed varieties of white and purple flowers
in a process called hybridization. The true breeding plants are the parental
generation or P generation. When the true breed white pea variety allows to cross-
pollinate to a true breed purple white pea variety, the offsprings have all purple
flowers. These flowers are already hybrids. This generation of offspring is called
the first filial generation or F1 generation. When these purple flowers were self-
pollinated, the offsprings have a ratio of 75% of purple flowers and 25% of white
flowers. This generation of offspsring is the second filial generation or F2
generation. Mendel called the purple flower dominant because they are the
majority of varities that are produced. The white purple flower are recessive
because they are produced lesser than the purple flowers.
Mendel’s experiment showed that the character traits, in this case the flower
color, are passed on from parents to offspring. Mendel concluded that there is a
heritable factor for a particuar trait that is passed on. This “heritable factor” of
Gregor Mendel is what we now call a gene.
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A
B
S
T
R
A
C
T
I
O
N
Figure 3.1.5. Seven character traits of pea plant used by Mendel in his experiment
Photo Credit: 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Aside from the pea’s flower color, Mendel also used other character traits of
pea plants in his experiment. The result of his experiment showed that, after cross
pollinating contrasting true-breeds of pea plant in P generation, it always produces
plants of the same character trait (e.g., all are tall plants) in the F1 generation. When
these F1 pea plants were allowed to self-pollinate, it results to pea plants with
character traits of 3:1 ratio (e.g., ¾ are tall plants, and ¼ of short plants. As he
repeated the experiment with the other character traits, it still produced the same
result. Mendel developed a hypothesis to explain the 3:1 inheritance pattern he
observed in F2 offspring.
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Mendel’s Model
For example, the gene for flower color in pea plants exists in two
versions, one for purple flowers and the other for white flowers
These alternative versions of a gene are now called alleles
Concept For each character an organism inherits two alleles, one from each
2: parent
Concept If the two alleles at a locus differ, then one (the dominant allele)
3: determines the organism’s appearance, and the other (the recessive
allele) has no noticeable effect on appearance
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Homozygous vs Heterozygous
Homozygous-- two identical alleles for a character.
Heterozygous-- two different alleles for a gene.
Phenotype vs Genotype
Phenotype refers to the physical appearance of an organism. It refers to any
observable traits in an organism such as its morpological, developmental,
biochemical, pysiological properties, or its behavior. The appearance of an
organism are determined either by genetic make-up or environmental factors.
Genotype refers to the genetic make-up of an organism. The genetic make-
up determines the physical traits (or phenotype of an organsim. Genotypes can be
homozygous dominant or homozygous recessive, and heterozygous. Homozygous
A
dominant are genotypes for dominant traits (e.g., purple color of flower in peas).
B
Homozygous recessive are genotypes for recessive traits. (e.g., white color of
S
flower in peas). Heterozygous consists of both dominant and recessive alleles.
T
R
A Writing of genotypes are
C denoted in letters. For
T homozygous dominant, letters
I are in uppercase; for example,
O PP—a genotype that determines
N the phenotype purple flower. A
purple color of flower in pea
plant is a dominant trait. For
homozygous recessive , letters
are in lower case; for example,
pp— a genotype that determines
the phenotype white flower as
white. A white color of flower
in pea plant is the recessive
trait. For heterozygous, letters
are both uppercase and
lowercase (Pp). Altough, in this
case, there is a recesssive allele, Figure 3.1.7 The phenotype (flower color) and
the heterozygous genotype Pp genotype (homozygous or heterozygous) of the
determines the purple fower pea flower
color of the pea. This is because
Photo Credit: 2008 Pearson Education, Inc., publishing as
the dominant allele masks the Pearson Benjamin Cummings
recessive allelle.
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a. The Law of Seggregation The law of segregation states that the two
alleles for a heritable character separate
(segregate) during gamete formation and end up
in different gametes
For example, an egg or a sperm gets only one of the two alleles that are
present in the somatic cells of an organism. This segregation of alleles
corresponds to the distribution of homologous chromosomes to different
gametes in meiosis
A Key Points:
B
S Mendel identified the law of
seggregation, by using a single
T
character (e.g., flower color).
R
These organisms that are
A
heterozygous for one
C character are called
T monohybrids. A cross
I between such hybrids are
O called monohybrid cross.
N Mendel’s segregation model
accounts for the 3:1 ratio he
observed in the F2 generation
of his numerous crosses
The possible combinations of
sperm and egg can be shown
using a Punnett square, a
diagram for predicting the
results of a genetic cross
between individuals of known
genetic makeup
A capital letter represents a
dominant allele, and a Figure 3.1.8. Test Cross of flowers with a
lowercase letter represents a single trait
recessive allele
Photo Credit: 2008 Pearson Education, Inc., publishing as
Pearson Benjamin Cummings
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A
B
S
T
R
A
C
T
I
O
N
Key Points:
Mendel identified the law of independent assortment, by using two character
traits of an organism which are dihybrids. Crossing two true breeding traits
of an orgaims results to dihybrids—both heterozygous. A cross between
such heterozygotes are called dihybrid cross.
Mendel’s model he identified in the second law accounts for the 9:3:3:1 ratio
he observed in the F2 generation of his numerous crosses.
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Sum It Up
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LESSON POST-TEST
How Much Have You Learned?
How much have you learned from the previous readings and
activities? This time, we will have our evaluation. Read the directions
carefully. Good luck! 😊
3. Which of the following is the most significant conclusion that Gregor Mendel
drew from his experiments with pea plants?
A. Recessive genes mask the dominant genes in the F2 generation
B. Traits are inherited in discrete units, and are not the results of
"blending."
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4. Of all the pea plants with 7 traits used by Mendel, he observed that it follows the
Law of Independent Assortment. Which of the folowing best accounts for this
result?
A. The ploidy type of chromosome do not determine the phenotype of the
offspring.
B. none of the traits obeyed the law of segregation.
C. all of the genes controlling the traits were located on the same
chromosome.
D. all of the genes controlling the traits behaved as if they were on different
chromosomes.
Ans. _______ Explanation:
5. In the Philippines, the dominant trait for the type of hair is straight. The recessive
trait is curly hair. Let’s assign letter S to denote the type of allele for the type of
hair. Which of the following denotes the homozygous dominant allele for the
trait?
A. Ss
B. SS
C. ss
D. SSS
Ans. _______ Explanation:
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7. It was important that Mendel examined not just the F1 generation in his breeding
experiments, but the F2 generation as well, because
A. he obtained very few F1 progeny, making statistical analysis difficult.
B. parental traits that were not observed in the F1 reappeared in the F2,
suggesting that the traits did not truly disappear in the F1.
C. analysis of the F1 progeny would have allowed him to discover the law of
segregation, but not the law of independent assortment.
D. the dominant phenotypes were visible in the F2 generation, but not in the
F1.
Ans. _______ Explanation:
9. Mendel accounted for the observation that traits which had disappeared in the F1
generation reappeared in the F2 generation by proposing that
A. new mutations were frequently generated in the F2 progeny, "reinventing"
traits that had been lost in the F1.
B. the mechanism controlling the appearance of traits was different between
the F1 and the F2 plants.
C. traits can be dominant or recessive, and the recessive traits were obscured
by the dominant ones in the F1.
D. the traits were lost in the F1 due to blending of the parental traits.
Ans. _______ Explanation:
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Self-Rating Journal
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Answer Key
LESSON PRE-TEST
1. C
2. D
3. C
4. B
5. D
6. D
7. D
8. B
9. C
10. D
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Introduction
LESSON PRE-TEST
What Do You Already Know?
Please check your background on the lesson by answering the
following pre-test. Do not sneak for an answer yet. You may check the
correct answers only after you have answered all questions. Read all
directions carefully.
Part I. Multiple Choice. Write the letter of the best answer. Then, explain your
answer.
2. Two plants are crossed, resulting in offspring with a 3:1 ratio for a particular trait.
This suggests
A. that the parents were true-breeding for contrasting traits.
B. incomplete dominance.
C. that a blending of traits has occurred.
D. that the parents were both heterozygous.
Ans. _______
Explanation:
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Ans. _______
Explanation:
Ans. _______
Explanation:
6. Black fur in mice (B) is dominant to brown fur (b). Short tails (T) are dominant
to long tails (t). What fraction of
A. the progeny of the cross BbTt × BBtt will have black fur and long tails?
1/16
B. 3/16
C. 3/8
D. ½
Ans. _______
Explanation:
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Page 114 EducSci 323A Genetics
10. What is genetic cross between an individual showing a dominant phenotype (but
of unknown genotype) and a homozygous recessive individual called?
A. a self-cross
B. a testcross
C. a hybrid cross
D. an F1 cross
Ans. _______
Explanation:
Check the correct answers found at the last page of the lesson
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Self-Rating Journal
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LESSON PROPER
Let’s start our lesson. You have a suggested time allotment of 3 hours to
finish all the readings, activities, and assessments. That is only a suggested
time frame. You may answer all the activities at your most convenient
time. Do not forget to read all instructions. Happy reading! 😊
Direction: I have here key terms for our lesson. Fill the missing letters to complete the
correct word.
3. __ENO__Y__E It is an individual’s collecion of genes. It can also refer to the two alleles
inherited for a partcular gene
V
O 4. HO__OZ__G__US DO__INA__T A__LE__E a genotype in which both alleles are
C dominant
A
B 5. __OM__ZY__O__S __ECE__SIVE __L__ELE a genotype in which booth alleles are
recessive
U
L 6. __ET__ROZ__GO__S A__LELE a genotype in which oe allele is dominant, the other
A allele is recessive.
R
Y 7. __H__NO__YPE any observable characteristics of an organsim such as the physical,
biochemical, and physiological characteristics
Check the correct answers found at the last page of the chapter
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Page 117 EducSci 323A Genetics
A
C
T
I
V
I
T Attached Earlobe Free earlobe
Y
1. Get a mirror. Touch your earlobe found at the bottom of your ear.
Using your mirror, observe if it is attached to the side of the head or
not.
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Page 118 EducSci 323A Genetics
3. If you know the type of earlobe of your parents, could you determine your
genotype for the earlobe already? How?
A
N
A
L
Y
S
I
S
Getting There...
What type of earlobes do you have? In humans, there are two types of
earlobes: the attached earlobe and the free earlobe. Some people have their
earlobes attached to the side of the head. This is the attached earlobe. Some
have unattached earlobes or free earlobes.
The free earlobe is due to a gene that is dominant for the trait. The
attached earlobe is due to a gene that is recessive for the trait. It is possible for
you to predict the type of gene for your earlobe if you know the genotype of
your parents. You could also predict a certain trait of your future offspring if
you know your genotype, and the genotype of your future life partner. It can
be illustrated through the use of punnet square. Let’s get to know more on
how to do it.
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Page 119 EducSci 323A Genetics
e e
3. Cross each allele. First is in the first box (e x E). Then, in the second box (e x
e)
eE eE
ee
ee ee
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Juan and Maria will have children that have free earlobes and attached
earlobes. Half of their children will have free earlobes. Half of their children
will have attached earlobes. For example, if they will have 8 children, 50%
of them (or 4/8) will have free earlobes, and 50 % of them (or 4/8) will have
attached earlobes.
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Page 121 EducSci 323A Genetics
Sample Problem 1
In dragons, wings are a dominant trait, but some dragons are born wingless.
1. If a wingless dragon is crossed with one that is heterozygous, how many of
its offspring will also be wingless?
2. What are the chances that two heterozygous dragons have a whelp that is
wingless?
Your Answer:
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Sample Problem 2
If a wingless dragon is crossed with one that have wings, How many of
the offspring are wingless? How many have wings? How can you
determine the genotype of the parent winged dragon?
Your Answer:
Check the correct answers found at the last page of the chapter
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Page 123 EducSci 323A Genetics
For example,
Cross heterozygous green pea (Gg) with heterozygous green pea plant
(Gg). Yellow is recessive.
Keys: GG gg -- yellow
Gg Green
G g
Parent cross: Gg x Gg G GG Gg
g Gg gg
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Sample Problem 1:
Your Answer:
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A test cross using a Punnet sqaure can be applied to two character traits that are
hybrids. This test cross is known as dihybrid cross. In In Mendel’s experiment, the
law of independent assortment can be illustrated by the dihybrid cross. To solve genetics
problems using dihybrid cross, take the following steps:
For example,
Test cross heterozygous with a genotype of TtTt (Tall
plant, short plant) and GgGg (Green pod, yellow pod)
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Punnett Square:
Genotype Phenotype
9/16 tall plant, green
pod
3/16 tall plant, yellow
pod
3/16 short plant,
green pod
1/16 short plant,
yellow pod
A
B Phenotypic ratio= 9:3:3:1
S All of these type of crosses will follow the same ratio:
T
R AaBb x AaBb both heterozygous for both traits
A
C 9 - (two dominant traits)
T 3 - (one dominant, one recessive)
I 3 - (one recessive, one dominant)
O 1- (two recessive traits)
N
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Page 127 EducSci 323A Genetics
Let’s go back to our activity with your earlobe. Now that you were
able to determine your type of earlobe (phenotype), let’s predict your
genotype.
1. Applying the learings you gained in this lesson, use a punnett
square to predict your hypothetical genotype for your earlobe.
A
P
P
L
I
C
A
T
I
O
N
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Sum It Up!
Punnett square is a diagram used to predict the phenotype and genotype of the
offspring.
A test cross is a way to determine whether an organism that is expressed a dominant
trait was a aheterozygote or a homozygote.
Monohybrid cross is the mating of two parents that are heterozygotes or hybrids that
involves a single trait .
Dihybrid cross is the mating of two parents that are heterozygotes or hybrids that
involves two traits.
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Page 129 EducSci 323A Genetics
LESSON POST-TEST
How Much Have You Learned?
How much have you learned from the previous readings and
activities? This time, we will have our evaluation. Read the directions
carefully. Good luck! 😊
I. Multiple Choice
Direction: Write the letter of the correct answer. Use a punnett square if it is
necessary and provide an explanation. Without an explanation and a punnett square,
points will not be valid. (2 points)
1. A sexually reproducing animal has two unlinked genes, one for head shape (H)
and one for tail length (T). Its genotype is HhTt. Which of the following genotypes
is possible in a gamete from this organism?
A. HT
B. Hh
C. HhTt
D. D) T
Ans. _______Explanation:
2. Two true-breeding stocks of pea plants are crossed. One parent has red, axial
flowers and the other has white, terminal flowers; all F1 individuals have red,
axial flowers. If 1,000 F2 offspring resulted from the cross, approximately how
many of them would you expect to have red, terminal flowers? (Assume
independent assortment.)
A. 65
B. 190
C. 250
D. 565
Ans. ______Explanation:
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Page 130 EducSci 323A Genetics
3. Given the parents AABBCc × AabbCc, assume simple dominance and independent
assortment. What proportion of the progeny will be expected to phenotypically
resemble the first parent?
A. ¼
B. 1/8
C. ¾
D. 3/8
Ans.
Explanation:
4. Skin color in a fish is inherited via a single gene with four different alleles. How
many different types of gametes would be possible in this system?
A. 1
B. 2
C. 4
D. 8
Ans.
Explanation:
Use the following diagram and description to answer the questions below.
In a particular plant, leaf color is controlled by gene D. Plants with the dominant
allele D have dark green leaves, and plants with the homozygous recessive dd
genotype have light green leaves. A true-breeding dark-leaved plant is crossed with a
light-leaved one, and the F1 offspring is allowed to self-pollinate. The predicted
outcome of this cross is diagrammed in the Punnett square shown below, where 1, 2,
3, and 4 represent the genotypes corresponding to each box within the square
5. Which of the boxes marked 1-4 correspond to plants with dark leaves?
A. 1 only
B. 1 and 2
C. 2 and 3
D. 1, 2, and 3
Ans.
Explanation:
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Self-Reflect
Write a reflective essay about your future self. Your essay should cover, but
not limited to the following:
1. Your favorite phenotype of yourself
2. Your offspring inheriting your favorite phenotype
3. Application of punnett square for predicting the phenotype of your
offspring.
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Answer Key
LESSON PRE-TEST
1. C
2. D
3. B
4. C
5. A
6. D
7. C
8. D
9. B
10. B
1. ALLELE
2. DOMINANT ALLELE
3. GENOTYPE
4. HOMOZYGOUS DOMINANT ALLELE
5. HEMOZYGOUS RECESSIVE ALLELE
6. HETEROYGOUS ALLELE
7. PHENOTYPE
8. RECESSIVE TRAIT
9. PUNNETT SQUARE
10. TEST CROSS
Sample Problem 1
1.) ff x Ff
f f
F Ff Ff
2.) Ff x Ff
F f
Ff Ff
F
Ff ff 25% of its offspring will be wingless.
f
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Sample Problem 2
ff x FF
f f
F Ff Ff
F Ff Ff
ff x Ff
f f
F Ff Ff
f ff ff
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Pp x Pp
P p
P PP Pp
p Pp Pp
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Page 136 EducSci 323A Genetics
Introduction
All living things pass on information from one generation to the next using the
same basic material, DNA. Within every living organism, most cells contain a
complete set of DNA instructions. The information in DNA tells our bodies how to
develop, grow, and work. It also controls many of the features that make an organism
unique.
Every cell contains DNA. Cells contain water, proteins, and Nucleic Acids
(DNA and RNA) contained in a membrane made of lipids (fat). In the following
activity, when you add soap to the cells of banana, it breaks the membranes open and
the contents of the cell, including the DNA, spill out. The salt changes the ionic
concentration of the water and makes it easier for the DNA and RNA to separate.
DNA will not dissolve in alcohol, so when you add alcohol to the solution, the DNA
collects where the two layers meet. In this activity, we will use common household
materials to break apart the cells in a banana and extract out its DNA.
Objectives
In this activity, you will:
1. Extract DNA from a riped banana.
2. Examine the nature of the extracted DNA from banana.
3. Explain the role of materials used in banana DNA extraction based on scientific
concepts and principles.
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Procedure
1. Mash a banana in a sealed thick clear plastic bag (e.g., ice-water bag). Add
about 1/3 cup of banana to the bag, remove the air, seal and then start squishing
it up. That’s about 1/3 a banana. Once it’s turned into a paste, set the bag aside.
2. Fill a clear glass with 1/2 cup of water. Slowly add in 2 teaspoons of dish soap
and 1/2 teaspoon of table salt. Gently mix this solution without making bubbles
until the salt dissolves. The salt will latter help the DNA stick together. Add this
solution to your sealed bag of squished up banana. Don’t add too much liquid.
Add enough so that you have a nice mixture that you cannot see through. That’s
probably about 1/4 of a cup of soap solution. Flatten out your baggie to remove
most of the air and then seal it up. Gently squish the liquid around. If you have
the time, let this mixture sit for 10-20 minutes to give the detergent time to
release a lot of DNA.
3. Place a coffee filter (or any clean filter paper) on top of a glass and carefully pour
your banana mixture into the filter. You can gently squeeze the filter to get more
liquid out, just don’t break it! This is the solution that contains the DNA.
4. Pour the cold rubbing alcohol (or ethyl alcohol will do) down the side of the
glass very carefully. You are trying to create a layer of alcohol that floats on the
top of the water solution. The DNA will come out of solution at the boundary
layer between the water and alcohol. You should see some white string almost
cotton like strands begin to appear in the glass. That is the DNA!
5. Let the solution sit for a few minutes and you should see more DNA come out
of the solution. You can collect the DNA using a toothpick, chopstick or
paperclip. You have extracted DNA at home!
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Guide Questions:
What does the banana DNA look like?
Why was the banana used in this activity? Can you use other fruits? If yes, why?
Why is it necessary to add a cold alcohol to the fruit mixture?
Why is it necessary to add salt to the fruit mixture?
Why is it necessary to add a liquid detergent to the fruit mixture?
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