B9 Genetic Diversity Flashcards
(51 cards)
What does meiosis produce and what does it involve
produces daughter cells that genetically Diff from each other.
involves two nuclear divisions and creates four haploid daughter cells from a single diploid parent cell
What are 2 mechanisms in meiosis that introduce variation
Independent segregation of homologous chromosomes
Crossing over between homologous chromosomes
Both occur in meiosis I (first round of division)
Independent segregation
In meiosis I, homologous pairs of chromosomes line up opposite each other at the equator of the cell.
It is random which side of the equator the paternal and maternal chromosomes from each homologous pair lie.
These pairs are separated, so one of each homologous pair ends up in the daughter cell.
Independent segregation - calculation
This creates a large number of possible combinations of chromosomes in the daughter cells produced.
This can be calculated using 2^n
n = number of homologous pairs
What is crossing over and how does it work
homologous pairs line up opp each other at equator in meiosis I, parts of chromatids twist around each other.
puts tension on chromatids, pairs of chromatid to break.
broken parts of chromatid recombine with another chromatid.
results in new combo of alleles.
Meiosis compared to mitosis
Meiosis
- 2 nuclear divisions
- haploid cells (one set of chromosomes)
- introduces genetic variation
Mitosis
- 1 nuclear division
- diploid cells (2 sets of chromosomes)
- create genetically identical cells
Identifying meiosis in a life cycle
Tip: Meiosis involves diploid (2n) parent cell dividing to become haploid (n) cell
Final increase in genetic variation
Random fertilisation further increases genetic variation.
There 2n possible chromosome combo in gametes ( 2^23 in humans)
It is random which egg and sperm will fuse is fertilisation. Therefore, variation is increased.
There is altuaily (2n)2 possible combinations of chromosomes when you consider random fertilisation.
For a human this = (2^23)^2 = 7.04 x 10^13
This is before crossing over is considered.
What’s non-disjunction
chromosomes or chromatids dont split equally during anaphase.
Chromosome mutations
Mutations in number of chromosomes arise spontaneously by chromosome non-disjunction during meiosis.
Chromosome non-disjunction
Changes in the number or structure of whole chromosomes can arise spontaneously due to chromosome non-disjunction during meiosis.
This can occur in two forms:
1. Changes in whole sets of chromosomes (polyploidy)
2. Changes in the number of individual chromosomes (aneuploidy)
What is polyploidy
Changes in whole sets of chromosomes occur when organisms have three or more sets of chromosomes rather than the usual two. This condition is called polyploidy and mainly occurs in plants.
Changes in whole sets of chromosomes occur when organisms have three or more sets of chromosomes rather than the usual two
What is aneuploidy
Changes in the number of individual chromosomes.
Sometimes individual homologous pairs of chromosomes fail to separate during meiosis.
This is non-disjunction and usually results in a gamete having one more or one fewer chromosome.
On fertilisation with a gamete that has the normal number of chromosomes, the resultant zygote will have more or fewer chromosomes that normal in all their body cells. E.g. Down’s syndrome is 3 copies of chromosome 21.
Aneuploidy
Changes in the number of individual chromosomes.
On fertilisation with a gamete that has the normal number of chromosomes, the resultant zygote will have more or fewer chromosomes that normal in all their body cells.
E.g. Down’s syndrome is 3 copies of chromosome 21.
What’s a mutation
Any change to quantity or base sequence of DNA of an organism
What’s a gene mutation
Any change to 1 or more nucleotide bases, or a change in the sequence of the bases in DNA
What’s produced by a mutation during hte formation of gametes
Mutations occurring during the formation if gametes may be inherited, often producing sudden + distinct differences between individuals.
When can a gene mutation arise spontaneously and what do they include
During DNA replication and include base substitution and base deletion
What is the gene mutation ‘substitution of bases’
Nucleotide base in DNA molecule is replaced by another nucleotide that has a different base
What’s the effect of the gene mutation base substitution of cytosine in GTC with guanine
DNA triplet of bases, GTC codes for amino acid glutamine.
It becomes GTG.
GTG codes for amino acid histidine + replaces original amino acid glutamine.
Polypeptide produced will differ in a single amino acid
Why might the base substitution gene mutation not have any effect
The new triplet of bases might still code for the same amino acid as before. So there’s no change in polypeptide produced + so mutation has no effect.
Due to degenerate nature of genetic code
What’s the gene mutation deletion of bases
Arises when nucleotide is lost from the normal DNA sequence
1 deleted nucleotide causes all triplets in a sequence to be read differently because each has been shifted to the left by 1 base.
What are chromosome mutations
Changes in the structure or number of whole chromosomes
When can chromosome mutations arise
Spontaneously