Genetic Recombination Flashcards
lecture 9 week 4
How does the location of two genes affect genetic outcome
- recombinant gametes are the result of independent assortment of chromosomes during meiosis 1 and are a major source of genetic variation
-independent assortment predicts that 50% of gametes will be non-recombinant and 50% recombinant
- alleles are exchanged on non-sister chromatids
- independent assortment and chromatid exchange leads to genetic variation
How does genetic outcome depend on physical location
- on the same chromosome (no change at any stage)
linkage: two genes on a single pair of homologues, no genetic exchange occurs
100% non-recombination - on the same chromosome
linkage: two genes on a single pair of homologues, exchange occurs between two non-sister chromatids
maximum 50% recombinants, depending on physical distance between genes - on different chromosomes
independent assortment: two genes on two different homologous pairs of chromosomes
50% recombinant and 50% non-recombinants - genes on same chromosome segregate together
What does F1 and F2 look like with genes on the same chromosome
F1: all F1 are heterozygous for both gene pairs and exhibit the dominant trait
top chromosomes on top line and bottom chromosomes on the bottom
F2: different to Mendelian dihybrid cross no 9:3:3:1 ration formed, 1:2:1 instead, one phenotype cannot be made die to physical location of two genes - no recombinant gametes
What happens when non-sister chromatids are crossed over
crossing over of non-sister chromatids can generate recombinant chromosomes as long as crossing over takes place during prophase of meiosis 1, then the exchange between non-sister chromatids forms a recombinant allele that did not exist before
How was recombination discovered
- Morgan introduced the notion of crossing over
- gene separation caused crossing over to occur at chiasmata, but Morgan could not explain results, why different frequencies of phenotypes occur
- then found meaning of different recombination frequencies, two genes that are very close together will have less chiasmata than genes very far apart
How is the relationship between meiotic events and phenotypic classes explained
- test crosses between a double heterozygous parent and double hemizygous recessive, then if recombinant crosses occur its from one crossover in meiosis when the parental female formed gametes
What are double cross-overs
double crossovers can only be identified when there are three genes linked on the same chromosome
- these are very infrequent as parents must be heterozygous for all three genes under consideration
- a triple heterozygous female is crossed with a male carrying recessive for all three genes
What are the crossing over events in meiosis 1
- for linked genes crossing over in meiosis 11 produces new genetic combination in the gametes
- for two genes on the same chromosome
no recombination is more likely than a single crossover and this is more likely than double crossovers
Questions using mapping units
1 map unit (cM) = 1% recombination
eg. if the distance between genes is 20 cM, how many of the 200 chromosomes will be recombinant
20cM = 20% recombination
20% of 200 is 40 so 40 chromosomes undergo recombination