Meiosis and mutations Flashcards
Compare and contrast meiosis and mitosis
Comparison=
- In both, DNA is replicated at the start
- In both the daughter cells produced can be haploid
Contrast=
- In meiosis there are 2 divisions but in mitosis there’s only 1 division
- In meiosis 4 daughter cells are produced whereas in mitosis only 2 are produced
- In meiosis, crossing over and independent segregation occur whereas they don’t in mitosis
- The daughter cells are genetically identical in mitosis whereas in meiosis they are genetically different
- In meiosis homologous chromosomes separate whereas they don’t in mitosis
State another way genetic variation increases (not crossing over or Independent seg.)
Random fertilisation of gametes happens after meiosis. Each gamete is fertilised with different alleles
Describe what happens during Independent segregation and explain how it creates genetic variation
When homologus pairs line up at the equator of the cell maternal and paternal chromosomes can form different combinations
Describe what happens during crossing over and explain how it increases genetic variation
- Homologus pairs of chromosomes associate to form a bivalent
- Chiasmata form
- Equal lengths of non- sister chromatids and alleles are exchanged
- This produces new combinations of alleles in the gametes
What is meant by haploid?
A haploid cell is a cell containing one of each type of chromosome e.g. a gamete
It is represented by n
What is meant by diploid?
A diploid cell is a cell containing 2 of each type of chromosome e.g. a normal body cell
It is represented by 2n
What is chromosome non-disjuction?
A spontaneous mutation that can occur in meiosis is called chromosome non- disjunction
Homologus chromosomes (1st division) or sister chromatids (2nd division) aren’t separate forming gametes with 1 more/ 1 less chromosome.
It can lead to genetic diseases like Down syndrome
What are homologus chromosomes?
Homologus chromosomes are a pair of chromosomes which have the same genes at the same gene loci but many have different alleles
What is a mutation and how does it arise?
A gene mutation is a change in the DNA base sequence of a chromosome which leads to the formation of a new allele.
A mutation can lead to the production of a non- functional enzyme. Explain how (7)
- mutation is a change in the DNA base sequence
- changes the amino acid sequence of a polypeptide
- changes the position of the hydrogen, ionic and disulphide bonds between amino acids
- changes the tertiary structure
- active site changes shape
- so active site isn’t complementary to the substrate
- no enzyme- substrate complexes form
Describe how a mutation can create a non- functional protein
- change in the DNA base sequence
- changes the amino acid sequences of the polypeptide
- changes the position of the hydrogen, ionic and disulphide bonds between amino acids
- changes the tertiary structure
Name some possible mutagenic agents
- High energy environments- X-rays, UV radiation
- Chemicals- benzene, asbestos
What is a deletion mutation?
when one base is removed from the DNA
Describe and explain the possible effect of a substitution mutation on a protein
Substitution mutations don’t always result in a change to the amino acid sequence. This is because the genetic code is degenerate so some amino acids are coded for by more than 1 triplet
What is a substitution mutation?
when one base is swapped for another base