Why might a mutation not lead to change in the amino acid sequence
Genetic code is degenerate so mutation may end up coding for the same amino acid as the original triplet
Mutation may occur in intron
What is a substitution mutation
When a base in the DNA base sequence is replaced by another
More likely to be a quiet mutation - meaning no change occurs in the amino acid sequence
Quiet mutation
No change occurs in the amino acid sequence
What is a deletion mutation
When a base in the DNA sequence is lost
More likely to be harmful - leads to a frame shift
The entire amino acid sequence will be different
Mutagenic agent
Factors that increase the rate of gene mutation
Examples of mutagenic agents
X-rays
UV light
Gamma rays
Chemical - tobacco and alcohol
What is a polyploidy chromosome mutation
Where an individual has 3 or more sets of chromosomes instead of 2
Chromosome non-disjunction
When chromosomes fail to separate correctly in meiosis resulting in gametes with one more/less chromosomes than normal
What is meiosis
A form of cell division that produces four genetically different haploid cells known as gametes
Haploid cells
Cells with half the number of chromosomes found in the parent cell
Meiosis vs mitosis - differences
Meiosis produces four genetically different cells with half the number of chromosomes as the parent cells
Mitosis produces two genetically identical cells with the same number of chromosomes as the parent cells
Meiosis 1
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Meiosis 2
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Drawdiagrams to show cells after each stage of meiosis
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Give 2 ways meiosis can produce genetic variation
Crossing over during meiosis 1
Independent assortment of homologous chromosomes and sister chromatids
Result in new combinations of alleles
Independent assortment
The production of different combinations of alleles in daughter cells due to the random alignment of homologous pairs along the equator of the spindle during metaphase I