Genetic and Inheritance
Genetic and Inheritance
Important keywords:
1. Chromosome: coils of DNA found in the nucleus of a cell.
2. Gene: section of DNA that contains genetic information or coding for a
protein
3. DNA: double helix structure - chromosomes and genes are made from
DNA. Deoxyribonucleic acid.
4. Allele: different variations of a gene
5. Genome: all genetic information in an organism
6. Genotype:
7. Phenotype: The observable characteristics of an organism (seen just by looking
– like eye colour, or found – like blood type) is called the phenotype
8. Homozygous: If the two alleles of a gene are the same, we describe
the individual as being homozygous
9. Heterozygous:
10. Dominant: A dominant allele only needs to be inherited from one
parent in order for the characteristic to show up in the phenotype
11. Recessive: A recessive allele needs to be inherited from both parents in
order for the characteristic to show up in the phenotype.
12. Haploid:
13. Diploid:
Genetic and Inheritance
3.17B understand that an RNA molecule is single-stranded and contains uracil (U) instead
of thymine (T)
There are three types
of RNA: tRNA, mRNA
and rRNA.
Thymine is replaced
by Uracil.
3.18B describe the stages of protein synthesis including transcription and translation,
including the role of mRNA, ribosomes, tRNA, codons and anticodons
Genetic and Inheritance
3.19 understand how genes exist in alternative forms called alleles which give rise to
differences in inherited characteristics
3.20 understand the meaning of the terms: dominant, recessive, homozygous,
heterozygous, phenotype, and genotype
3.21B understand the meaning of the term codominance
3.22 understand that most phenotypic features are the result of polygenic inheritance
rather than single genes
3.23 describe patterns of monohybrid inheritance using a genetic diagram
Knowing how inheritance works allows you to inherit special family tree diagrams
showing genetic disorders.
These are called family pedigree charts.
3.26: understand how the sex of a person is controlled by one pair of chromosomes, XX in
a female and XY in a male
3.27: describe the determination of the sex of offspring at fertilisation, using a genetic
Diagram
3.28: understand how division of a diploid cell by mitosis produces two cells that contain
identical sets of chromosomes
3.29: understand that mitosis occurs during growth, repair, cloning and asexual
Reproduction
Mitosis is the process of dividing the bodies cells in 2 and their nuclei. This celld
ivsion prodices more cells. These produce genetically identical copies of the
parent cell. It is in asexual reproudction. Genetic stabillity.
- Helps us grow
- Repairs damage to the body
8.
Chromatics centromiere
Recombinant chromosomes
Genetic and Inheritance
Metaphase
Chromosomes
Anaphase
Genetic and Inheritance
Telophase
3.30 understand how division of a cell by meiosis produces four cells, each with half the
number of chromosomes, and that this results in the formation of genetically different
haploid gametes
3.31 understand how random fertilisation produces genetic variation of offspring
3.32 know that in human cells the diploid number of chromosomes is 46 and the haploid
number is 23
3.33 understand that variation within a species can be genetic, environmental, or a
combination of both
3.34 understand that mutation is a rare, random change in genetic material that can be
inherited
3.35B understand how a change in DNA can affect the phenotype by altering the
sequence of amino acids in a protein
3.36B understand how most genetic mutations have no effect on the phenotype,
some have a small effect and rarely do they have a significant effect
3.37B understand that the incidence of mutations can be increased by exposure to
ionising radiation (for example, gamma rays, x-rays and ultraviolet rays) and some
chemical mutagens (for example, chemicals in tobacco)
3.38 explain Darwin’s theory of evolution by natural selection
3.39 understand how resistance to antibiotics can increase in bacterial populations, and
appreciate how such an increase can lead to infections being difficult to control
Transcription is the formation of RNA from DNA. The DNA gets unzipped temporarily so
the two strands separate.
Trna
Amino acids are joined together by peptide bonds
Translation is amino acids that are
3 nitrogen bases
3 nitrogen bases that code for one amino acids is known as a codon
A and T
C and G
Silent mutations
Harmful mutations
Deletion
Insertion
Substitution
Chemcilas that cause mutation are called mutigens
Gene: gene is the section of the DNA that codes for a protein.
Phenotype:
Homozygous:
Heterozygous:
Dominant:
Recessive:
Genotype:
Allele: these are variations of the same gene \
Long dna molecules that contains all the genetic information of an organism
Made up of nucleotides
Deoxyribonucleic acid
Adenine
Thymine
Cytosine
Guanine
Mitosis produces cells that are described as diploid; they contain the full number
of chromosomes. Sperm cells and egg cells; however, are described as being
haploid, they have half the full number of chromosomes. Gametes are produced
not by mitosis but by meiosis, a reduction cell division.
When two different
gametes combine this gives rise
to genetic variation.
Independent assortmennt
Crossing over
These cells are known as Gametes (sex cells; i.e. sperm and egg cells).
There is Genertic vairation
1. Mitosis produces two daughter cells only from one parent cell splitting in two. It
forms 2 diploid cells
2. Meiosis produces 4 daughter cells from mitosis 1 and mitosis 2. It forms 4 haploid
gamete cells for reproduction.
3. In mitosis, there is genetic identity but in meiosis there is genetic variation
because the daughter cells are not exactly idecombination can be defined as a
process by which the gene present on a particular chromosome can be
separated, and thus a new combination of genes would be formed.entical to the
parent cells. Another reason for genetic variation is the process known as
recombination.
4. Recombination
5. In meiosis there is independent assortment of genetical infromation and crossing
over.
6. Mitosis takes place in somatic cells, used for body cell’s regeneration.
7. Meiosis takes place in reproductive cells, results in formation of gametes
Genetic and Inheritance
Mutation
Mutation:
Mutation is a rare, random change in genetic material or DNA of an
orgasmin that can be inherited
● As the DNA base sequence determines the sequence of amino acids that
make up a protein, mutations in a gene can sometimes lead to a change in
the protein that the gene codes for