Genetic Recombination Flashcards

lecture 9 week 4

1
Q

How does the location of two genes affect genetic outcome

A
  • 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
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2
Q

How does genetic outcome depend on physical location

A
  • 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
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3
Q

What does F1 and F2 look like with genes on the same chromosome

A

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

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4
Q

What happens when non-sister chromatids are crossed over

A

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

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5
Q

How was recombination discovered

A
  • 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
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6
Q

How is the relationship between meiotic events and phenotypic classes explained

A
  • 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
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7
Q

What are double cross-overs

A

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
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8
Q

What are the crossing over events in meiosis 1

A
  • 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
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9
Q

Questions using mapping units

A

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

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