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GR 12 DNA Core Notes

This document discusses DNA, its structure, location, and role. It begins by explaining that DNA and RNA are found in all living organisms and are located in the nucleus and cytoplasm. It then discusses the discovery of DNA and its double helix structure composed of nucleotides. DNA is found primarily in the nucleus, but some is also located in mitochondria and chloroplasts. The structure of DNA allows it to self-replicate and transcribe genetic information via transcription and translation. Protein synthesis occurs through this process. Mutations in the DNA sequence can affect protein structure.

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0% found this document useful (0 votes)
106 views14 pages

GR 12 DNA Core Notes

This document discusses DNA, its structure, location, and role. It begins by explaining that DNA and RNA are found in all living organisms and are located in the nucleus and cytoplasm. It then discusses the discovery of DNA and its double helix structure composed of nucleotides. DNA is found primarily in the nucleus, but some is also located in mitochondria and chloroplasts. The structure of DNA allows it to self-replicate and transcribe genetic information via transcription and translation. Protein synthesis occurs through this process. Mutations in the DNA sequence can affect protein structure.

Uploaded by

joshdevree3
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Introduction

Activity 2: DNA
Revision of cellular structure replication

The structure of nucleic acids DNA profiling All living organisms contain both DNA (deoxyribonucleic acid) and RNA
(ribonucleic acid) we focus on their location, structure and function.
DNA deoxyribonucleic acid Activity 3: DNA profiling
We explore the discovery of DNA, its role in the human body and how it
A brief history of the discovery of Protein synthesis replicates.
DNA
Protein synthesis is vital for life we examine how proteins are formed by
Protein synthesis occurs in two
both DNA and RNA.
The location of DNA stages

The structure of DNA Stage 1: Transcription

The role of DNA Stage 2: Translation


It is important to know the location and functions of certain organelles, illustrated in
Activity 1: DNA The effect of mutation on protein Figure 1 below.
structure (DNA sequence)
RNA ribonucleic acid
Activity 4: Protein cytoplasm
The location of RNA synthesis
polysomes
The structure of RNA Activity 5: Codons and
The role of RNA amino acids
ribosomes
Comparison between DNA and RNA

DNA replication nucleus


End of topic exercises
Errors that occur during DNA
replication
Figure 1: Structure of a cell

Cytoplasm is the base substance in which the organelles of the cell are
suspended. It is a watery substance and allows for metabolic reactions to take place.
Ribosomes are small, round organelles which are mainly found attached to the
endoplasmic reticulum or are free-floating in the cytoplasm. Ribosomes can also be
found inside other organelles such as the chloroplast and mitochondria but in smaller
numbers. They are the site of protein synthesis and consist of RNA and protein.

6 7
The nucleus ities. The basic structure of a nucleotide is illustrated in Figure 3 below. Each nucleic acid
is composed of a phosphate (P), a sugar molecule (S) and a nitrogenous base (NB).

P phosphate group
S sugar molecule
NB nitrogenous base

Figure 3: A nucleotide

Figure 2: Parts of the nucleus

A nucleus has four main parts:


the double nuclear membrane it encloses the nucleus and contains small Key terminology
pores to allow for the passage of substances in and out of the nucleus deoxyribonucleic acid is made up of nucleotides
nitrogenous bases adenine, thymine, guanine and
DNA
the nucleoplasm this is a jelly-like fluid within the nucleus cytosine
carries the genetic code for protein synthesis
the nucleolus a dark body suspended in the nucleoplasm which contains
nuclear DNA DNA found in the nucleus
free nucleotide bases and produces ribosomes DNA found outside of the nucleus: mitochondrial and
extra- nuclear DNA
the chromatin network found in the nucleoplasm: contains the DNA which chloroplastic DNA.
forms the chromosomes containing the genetic code of a person / organism the shape of DNA consists of two strands joined together
double helix
and twisted spirally
hereditary genetic information passed on from parent to offspring

Key terminology 1952 Rosalind Franklin and her assistant Maurice Wilkins researched the
nucleic acid a type of organic compound structure of DNA using X-ray diffraction images.

monomer a building block Watson and Crick did


images, they proposed a 3-D double helix model for DNA in 1953.
nucleotide the monomer which forms DNA and RNA
1962 Watson and Crick received the Nobel Prize for the discovery of the
structure of DNA, and Wilkins received an award for his X-ray photography.
There are two types of nucleic acids in the human body DNA (deoxyribonucleic Franklin had died of cancer.
acid) and RNA (ribonucleic acid). Together these form the basis of all life of earth.
They consist of monomers (building blocks) called nucleotides.
Rosalind Franklin background: https://www.youtube.com/watch?v=BIP0lYrdirI

8 9
Nitrogenous bases are complementary, and always join together in a specific order:
adenine always links to thymine (Figure 5A)
DNA is found in two locations in a cell: guanine always links with cytosine (Figure 5B)
Mostly in the nucleus of a cell this is referred to as nuclear DNA
a small amount is found outside the nucleus it is referred to as extra- adenine guanine
nuclear DNA. There are two types of extra-nuclear DNA:
o chloroplastic DNA found in the chloroplasts of plant cells
o mitochondrial DNA found in the mitochondria (useful for tracing thymine cytosine
ancestry)

Figure 5A: adenine with thymine Figure 5B: guanine with cytosine

This pairing of bases means that two strands of DNA are joined together, forming a
long ladder-like structure. The nitrogenous bases are held together by weak
hydrogen bonds. The ladder-like structure becomes coiled and is known as a double
helix structure. The DNA strands wind around proteins which are known as
histones.

DNA carries hereditary information in the form of genes. Genes are short sections of
DNA which code for a specific trait, and determine the physical characteristics (e.g.
blood grouping, a gene linked to breast cancer) and behaviour of an organism (e.g.
whether an organism can be tamed and domesticated).
Most of the DNA strands do not code for anything and are known as non-coding
DNA. Scientists are still researching the importance of the non-coding DNA.
The main functions of DNA include:
Figure 4A: DNA double helix Figure 4B: DNA simplified structure
Controls the functioning of cells

DNA has a double helix structure (Figure 4A), consisting of monomers called Regulate the functioning of genes
nucleotides which link to form long chains, called polymers. The sugar in DNA is Passes on hereditary characteristics
deoxyribose sugar and is attached to a nitrogenous base. The phosphate and sugar
molecules are attached to one another by strong bonds alternately to form the long
chains (Figure 4B). The structure of DNA: https://www.youtube.com/watch?v=C1CRrtkWwu0

There are four types of nitrogenous bases in DNA:


adenine (A) cytosine (C)
thymine (T) guanine (G)

10 11
Activity 1: DNA
The diagram on the next page shows part of a DNA molecule.
1. Label parts 1, 2 and 3 (3) Messenger RNA (mRNA) is formed in the nucleus but then enters the
cytoplasm where it attaches to ribosomes.
2. Give the number of nucleotides
shown in the diagram (1) Ribosomal RNA (rRNA) is found in the ribosomes in the cytoplasm of the
cell.
3. Name two places in an animal
cell where this nucleic acid may Transfer RNA (tRNA) is found freely in the cytoplasm of the cell.
be found. (2)
4. What is the natural shape of
this molecule? (1)
5. Draw a nucleotide with the Like DNA, RNA also consists of monomers (nucleotides) which link to form longer
nitrogenous base adenine. (4) chains (polymers).
(11)
However, RNA is a single-stranded structure which is not coiled. The sugar in
RNA is ribose and is attached to a nitrogenous base. The phosphate and sugar
molecules are attached to one another alternately to form the chains.
The structure of RNA is illustrated in Figure 6 below.

Key terminology
RNA consists of nucleotides. Nitrogenous bases found in
RNA
RNA are adenine, uracil, guanine and cytosine
mRNA carries the code for protein synthesis from DNA to the
messenger RNA
ribosome
ribosomal RNA rRNA forms ribosomes which are the site of protein synthesis
transfer RNA tRNA brings amino acids to the ribosome to form the protein

There are three types of RNA (ribonucleic acid), all formed in the nucleus by DNA.
They perform different functions in different places in a cell. The types are:
messenger RNA (mRNA) Figure 6: RNA note the chain formed by the
phosphate and sugar molecules on the left,
ribosomal RNA (rRNA) and the nitrogenous bases on the right.
transfer RNA (tRNA)

There are four types of nitrogenous bases in RNA:

12 13
cytosine (C) 1. The DNA double helix unwinds 2. The weak hydrogen bonds between the
adenine (A) nitrogenous bases are broken. The DNA
(Figure 7A)
uracil (U) not thymine as in DNA guanine (G) strands separate (they unzip)(Figure 7B)

The three types of RNA are very important to the process of protein synthesis, with
Figure 7A Figure 7B
each type playing a unique role.

DNA and RNA are similar


contain sugar alternating with phosphate
contain the nitrogenous bases adenine, guanine and cytosine
play a role in protein synthesis

DNA and RNA also have significant differences, tabulated in Table 1 below. 3. Each original DNA strand 4. Free nucleotides build a DNA strand onto
serves as a template on which its each of the original DNA strands, attaching
Table 1: The main differences between DNA and RNA. complement is built (Figure 7C) their complementary nitrogenous bases
(A to T and C to G) (Figure 7D)

contains deoxyribose sugar contains ribose sugar


double helix and coiled single stranded
contains the nitrogenous base thymine contains the nitrogenous base uracil
found in the nucleus, ribosomes and
found in the nucleus only
cytoplasm of cells

A comparison DNA and RNA. It is very important to know the differences.


https://www.youtube.com/watch?v=0Elo-zX1k8M

DNA replication is the process through which DNA makes an identical copy of itself. Figure 7D
Figure 7C
This occurs during interphase of the cell cycle in the nucleus. In Figures 7A to 7E, a
small portion of DNA is shown undergoing replication.

14 15
5. This results in two identical DNA molecules. Each molecule consists of one
original strand and one new strand (Figure 7E).

4
A 1
Figure 7E
G

1. Name the process illustrated in the diagram above. (1)


Figure 7A 7E: The process of DNA replication 2. State the significance of the process mentioned in question 1. (1)
3. Identify the parts labelled as 1, 2, 3 and 4. (4)
DNA replication is important for cell division, particularly mitosis. It allows each 4. Describe how this process takes place. (6)
chromosome to be copied so that each new identical daughter cell produced 5. Give one location of extra-nuclear DNA. (1)
contains the same number and type of chromosomes.
(13)

Errors that occur during DNA replication may sometimes lead to mutations (a
change in the nitrogenous base sequence)
A DNA profile is a pattern produced on X-ray film. This pattern consists of lines
If the incorrect nitrogen base attaches to the original strand and a nitrogen base which are of different lengths and thicknesses and in different positions, as shown in
Figure 8. All individuals, except identical twins, have a unique DNA profile.
o the sequence or order of the bases c
o resulting in a change in the gene structure

DNA replication: Understand the process.


https://www.youtube.com/watch?v=Qqe4thU-os8

Activity 2: DNA replication

Study the diagram below and answer the questions that follow.
Figure 8: DNA profiles for three different
individuals.

16 17
DNA profiles are used to: In a fight involving a number of people, one person was seriously injured. Police took
blood samples from the victim, the crime scene (CSS crime scene sample) and
identify crime suspects in forensic investigations
four suspects. The DNA was then extracted from each sample. The results of these
prove paternity (father) and maternity (mother) (biological parents) tests are shown in the diagram above.
determine the probability or causes of genetic defects 1. Which suspect probably injured the victim? (1)
establish the compatibility of tissue types for organ transplants
2. Give a reason for your answer to the previous question. (1)
identify relatives
3. List one application of DNA profiling other than for solving crime. (1)
DNA profiling is generally accepted as being extremely reliable. The interpretation 4. Give two reasons why DNA profiling may sometimes be challenged. (2)
and comparison of profiles should however be approached with caution, for the (5)
following reasons:
Humans interpret the results which means mistakes could be made

The method of profiling may be different in different laboratories producing


inconsistencies Key terminology
Only a small piece of DNA is used in profiling, so the profile might not be amino acids monomers of proteins
100% unique to a particular individual base triplet three nitrogenous bases one after the other on DNA
DNA profiling is expensive and therefore not readily accessible to those who 1 stage of protein synthesis mRNA formed from DNA
transcription
cannot afford it, particularly in criminal cases carrying code for the protein to be made
2 stage of protein synthesis amino acids combine to form
DNA profiles may reveal information about a person which could be used translation
a protein
against them in a prejudicial way. For example: being HIV positive or having
three nitrogenous bases one after the other on mRNA
genetic abnormalities may lead to insurance companies not covering a codon
these are complementary to the triplet on DNA
person or prejudice in the court room
three nitrogenous bases one after the other on tRNA these
anti-codon
are complementary to the codon on mRNA
Activity 3: DNA profiling
DNA profiles from a crime scene. The process in which proteins are made is called protein synthesis. Proteins are
made by linking various amino acids that are present in the cytoplasm of cells. There
Victim CSS Suspect 1 Suspect 2 Suspect 3 Suspect 4
are 20 different amino acids, and they combine in a large variety of combinations.
The number of amino acids and the sequence of the amino acids determine the type
of protein that is formed.
Figure 9 illustrates a protein with different amino acids represented by the different
shapes and colour. The bond between the amino acids is known as a peptide bond.

peptide bond

Figure 9: Amino acids linked by peptide bonds

The genes found in DNA contain the code which determines which type of protein
that will be formed.

18 19
The smallest protein contains 50 amino acids linked together 1. A section of the DNA double helix unwinds. As a result,
Proteins generally contain 300 or more amino acids. the weak hydrogen bonds between the nitrogenous bases of DNA break

Three consecutive nitrogenous bases on the DNA strand are called the base triplet. the DNA unzips (in this particular section of the DNA)
The base triplets determine which amino acid will be placed into the protein as well 2. One strand acts as a template
as the sequence in which the amino acids will be joined.
3. This DNA template is used to form a complementary strand of messenger
RNA (mRNA)
This is done using free RNA nucleotides in the nucleoplasm
The mRNA now contains the code for the protein which will be formed
Stage 1: Transcription
Three adjacent nitrogenous bases on the mRNA are known as codons.
Stage 2: Translation These code for a particular amino acid.
4. mRNA moves out of the nucleus through a nuclear pore into the cytoplasm,
where it attaches onto a ribosome

The first stage of protein synthesis, called transcription, occurs in the nucleus (see
Figure 10 below).

The second stage of protein synthesis, called translation (Figure 11) , occurs in the
cytoplasm.
DNA

Stage 2
amino acid
nucleus cytoplasm
mRNA transcription protein forming tRNA with amino acid
cytoplasm

mRNA
mRNA

transport to cytoplasm for


next phase of protein
synthesis
translation

Figure 10: Transcription Figure 11: Translation

20 21
5. Transfer RNA (tRNA) in the cytoplasm has three adjacent nitrogenous bases Note: it is important to know the difference between base triplets (DNA), codons
known as the anti-codon (mRNA) and anti-codons (tRNA).
-codon
Each tRNA will carry a specific amino acid
According to the codons on the mRNA, the tRNA will bring the required
amino acid to the ribosome
6. The amino acids are linked by a peptide bond to form the required protein. A mutation is a change in the nitrogenous base sequence of a DNA molecule
(or a gene)
since mRNA is copied from the DNA molecule during transcription.
Figure 12 below shows the full process of protein synthesis
This will result in a change in the codons.
As a result, different tRNA molecules carrying different amino acids will be
required.
The sequence of amino acids changes, resulting in the formation of a different
protein.
DNA If the same amino acid is coded for, there will be no change in the protein
structure.

nucleus
Protein synthesis: https://www.youtube.com/watch?v=oefAI2x2CQM&t=43s

mRNA
Activity 4: Protein synthesis
The diagram below represents a process that occurs during protein synthesis.
cytoplasm
transport to cytoplasm for
the next phase of protein B
tRNA

mRNA
A

C
cell membrane

D
E

Figure 12: Protein synthesis 1. Identify the process above. (1)

22 23
2.
DNA The code of life: End of topic exercises
a) organelle A (1)
b) molecule B (1)
c) the bond at E (1) Section A

3. Question 1

a) carries the amino acid (1) 1.1 Various options are provided as possible answers to the following questions.
b) is the monomer of a protein (1) Choose the correct answer and write only the letter (A- D) next to the
question number (1.1.1 1.1.5) on your answer sheet, for example 1.1.6 D
4. Name and describe the process occurring in the nucleus which results in the
formation of the mRNA molecule. (6)
1.1.1 A molecule of RNA is copied from DNA by the process of
(12)
A transcription.
Activity 5: Codons and amino acids B mitosis.
C mutation.
The sequence of amino acids in a protein molecule is coded for by DNA and RNA.
D translation.
The table below shows some mRNA codons and the corresponding amino acids.
1.1.2 In a DNA molecule
mRNA codons amino acid
A guanine pairs with adenine.
AGC serine
B adenine pairs with thymine.
GAU aspartate C cytosine pairs with adenine.
CUA leucine D Guanine pairs with thymine.
UAU tyrosine
UUC phenylalanine 1.1.3 A codon is a sequence of three nucleotides on a molecule of
AGU serine A rRNA.
GAC aspartate B mRNA.
UUU phenylalanine C tRNA.
D DNA.
CUC leucine
GAG glutamic acid 1.1.4 DNA was analysed and found to contain 14% T (thymine). What
percentage of the molecule is cytosine?
1. According to the table, how many codons code for phenylalanine? (1)
A 14%
2. What is the anti-codon for glutamic acid? (1) B 28%
3. A section of mRNA has the following base sequence and is read from left to C 36%
right: D 72%

GAU CUC GAC AGC AUG ACC 1.1.5 A gene in a bacterium codes for a protein that has 120 amino acids.
Give How many mRNA nucleotides code for this protein?
A 30
a) DNA base triplet for the last codon on this section of mRNA (1)
B 40
st
b) 1 amino acid coded for by this section of mRNA (1) C 360
(4) D 480 (5 × 2 = 10)

24 25
1.2 Give the correct biological term for each of the following descriptions. Write 1.4 The diagram below represents a portion of a nucleic acid.
only the term next to the question number.

1.2.1 Proteins that form part of the chromosomes.


1.2.2 Which type of RNA travels from the nucleoplasm to the cytoplasm.
1.2.3 The nitrogenous base found in RNA but not in DNA.
1.2.4 A sugar that is a component of DNA.
1.2.5 A sudden change in the sequence / order of the nitrogenous bases
of a nucleic acid.

1.2.6 The name of the bond that forms between amino acids in a protein
molecule.
1.4.1 Name the nucleic acid. (1)
1.2.7 The type of nucleic acid that carries a specific amino acid.
1.4.2 Name two places in animal cells where this nucleic acid may be
1.2.8 A segment of DNA coding for a particular characteristic. found. (2)
1.2.9 The bonds that form between nitrogenous bases in a DNA, 1.4.3 Identify
a) portion 1 (1)
1.2.10 The organelle in the cytoplasm on which protein synthesis occurs.
b) nitrogenous base 3 (1)
(10 x 1) = (10)
c) molecule 5 (1)
d) bond 2 (1)
1.3 Indicate whether each of the descriptions in Column I applies to A ONLY, B 1.4.4 What is the natural shape of this molecule? (2)
ONLY, BOTH A AND B or NONE of the items in Column II. Write A only, B 1.4.5 Name the process in which this molecules make a copy of itself? (1)
only, both A and B or none next to the question number. (10)

Column I Column II 1.5 The diagram below represents DNA replication.


A: DNA
1.3.1 Contains ribose sugar
B: RNA
A: Mendel
1.3.2 Discovery of DNA
B: Darwin
A: nucleus
1.3.3 Location of DNA.
B: mitochondria
1.3.4 The process where one DNA A: replication
molecule produces two
B: reproduction
identical DNA molecules.
A: DNA
1.3.5 Pairing of nitrogenous bases
B: RNA

(5 x 2) = (10)

26 27
1.5.1 Identify the following: 2.1.3. Name and describe the process occurring in the nucleus which results
a) molecules W and U (2) in the formation of an mRNA molecule. (6)

b) parts of molecule W labelled X and Y (2) 2.1.4. Draw a RNA nucleotide with a complementary base to adenine. (2)
c) bond Z (1) (14)
d) nitrogenous base V (1)
1.5.2 Where in the cell does this process take place? (1) 2.2 The diagrams below represent the process of protein synthesis. Study them
1.5.3 Name the phase of the cell cycle where replication takes place. (1) and answer the questions that follow.
1.5.4 What is the purpose of DNA replication? (2)
(10)
Section A: [50]

Section B
Question 2

2.1 The following sequence represents a part of the nitrogenous base sequence
on a DNA molecule.

TAC TCT CCA


Triplet 1 Triplet 2 Triplet 3
2.1.1. Write down the base sequence of the anticodon of triplet 1 shown
above. (1)
2.1.2. The table below shows the amino acids that correspond with different
mRNA codons.
mRNA codon Amino Acid
AGA arginine
AUG methionine
GGU glycine
AUC isoleucine
2.2.1 Identify the structures labelled 1,2 and 3. (3)
a) Give the correct sequence of amino acids for DNA triplets
1 to 3. (2) 2.2.2 Name and describe the stage of protein synthesis taking place
at Z (5)
b) During DNA replication a mutation occurred on triplet 1 resulting
in C being replaced by G. Describe how this mutation will affect 2.2.3 Using the table below, work out the names of the amino acids
the structure of the protein formed. (3) labelled W and X. (4)

28 29
b) codon for proline (2)
Base Triplet on mRNA coding 3.1.5 State two differences between a DNA nucleotide and an RNA
Amino acid coded for
for the amino acid nucleotide. (4)
GAG glutamate (17)
CAG histidine
AGG arginine
3.2 The first 7 triplets of nitrogenous bases that form part of the gene coding for
CUG leucine
one chain of the haemoglobin protein that makes up red blood corpuscles in
UCC proline humans is shown below. Study the table and answer the questions that
GUG valine follow.
(12) DNA
CAC GTG GAC TGA GGA CTC CTC
[26] Template
Question 3 Base
3.1 The diagram below represents two stages of protein synthesis. triplet 1 2 3 4 5 6 7
number

3.2.1 How many of the following are coded for in the DNA template
sequence above?
a) Nitrogenous bases (1)
b) Different types of tRNA molecules that are required to form the
polypeptide from this piece of DNA . (1)
3.2.2 Write down the mRNA sequence for the triplets numbered 4 and 6
in the above table. (2)
3.2.3 Using the table below, determine the amino acid sequence
coded for by triplet numbers 4 and 6. (2)

3.1.1 Provide labels for: Anticodons on tRNA


coding for the amino Amino acid coded for
a) molecule 1 (1) acid
b) organelle 6 (1) CUC glutamate
3.1.2 Give only the number of the part which represents a:
GUC histidine
a) DNA template strand (1)
GGA proline
b) monomer of proteins (1)
GAC leucine
c) codon (1)
UGA threonine
3.1.3 Describe translation as it occurs in organelle 6. (4)
CAC valine
3.1.4 Provide the:
a) DNA sequence that codes for glycine (2)

30 31
3.2.4. If the T in the 6th base triplet changed to A in the DNA template
above, write down the new amino acid (using the table above) that
this 6th triplet now codes for. (1)
(7)
[24]

Section B: [50]

Total Marks: [100]

32

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