2 - Linkage, Recombination & Deviations from Mendelian Ratios Flashcards

1
Q

which 4 processes contribute to genetic variation?

A
  1. mutation
  2. independent assortment of chromosomes during meiosis I
  3. crossing over between homologous chromosomes during meiosis I
  4. random fertilisation of ova by sperm
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2
Q

how does independent assortment + random fertilization promote genetic variation?

A
  • The choice of which sperm fuses with which egg is random
  • With 8,388,608 kinds of sperm and 8,388,608 kinds of eggs, the no. of possible chromosome combinations in the offspring from one couple is >70,000,000,000,000
  • crossing over adds even more variation
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3
Q

recombinant phenotype

A

where the combination of phenotypes differs from that found in either of the parents

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4
Q

how do recombinant phenotypes occur?

A

through either independent assortment or crossing over

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5
Q

what is crossing over?

A

the process of genetic recombination that gives rise to new combinations of linked genes

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6
Q

crossing over explained

A
  • Occurs during the pachytene phase of prophase I
  • Begins with synapsis - pairing of homologous chromosomes
  • The synaptonemal complex is a protein ‘zipper’ that holds homologous chromosomes together in the tetrad
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7
Q

what is the result of crossing over?

A

recombinant chromosomes with new combinations of linked genes

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8
Q

recombinant frequency

A

percentage of the progeny that inherit a combination of alleles that differs from either parent

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9
Q

what are the results of a testcross when genes are on different chromosomes?

A

50% parental, 50% recombinant

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10
Q

what are the results of a testcross when genes are on the same chromosomes?

A

> 50% parental

<50% recombinant

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11
Q

who was the first to discover gene linkage?

A

T.H.Morgan using fruit flies

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12
Q

testcross involving the linked genes black (b) and vestigial (vg)

A

Mutants are given a name that reflects their phenotype - usually abbreviated e.g. black (b) and vestigial (vg)
recombinant frequency = 17%

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13
Q

what are the 2 possible arrangements of alleles in a double heterozygote?

A

coupling and repulsion

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14
Q

coupling heterozygote testcross outcome

A
parentals = b+ vg+ and b vg 
recombinants = b vg+ and b+ vg
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15
Q

repulsion heterozygote testcross outcome

A
parentals = b vg+ and b+ vg 
recombinants = b+ vg+ and b vg
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16
Q

what do multiple crossovers lead to?

A
  • an underestimate of the distance between 2 loci

- recombinant frequencies >50% are not possible

17
Q

3 point cross

A

allows the detection of double crossovers such that genes can be put into order

  • largest numbers = parental types
  • smallest numbers = double crossover
18
Q

who created chromosome maps?

A

A.H> Sturtevant (1913)

He saw that the recombination freq. between 2 genes should be related to their distance apart on the chromosome

19
Q

what are the 6 deviations from Mendelian ratios?

A
sex-linkage, 
incomplete dominance, 
co-dominance, 
pleiotropy, 
polygenic inheritance, 
epistasis
20
Q

sex linkage

A

occurs when certain traits are determined by genes on sex chromosomes

21
Q

occurs when certain traits are determined by genes on sex chromosomes

A

the sex chromosome found only in males.

cannot carry a gene

22
Q

incomplete dominance

A

Where a dominant allele does not completely mask the effect of a recessive allele at the same locus

23
Q

co-dominance

A

Where each allele affects the phenotype in separate, distinguishable ways

24
Q

incomplete dominance compared to codominance

A
  • incomplete dominance = blending of traits and a ‘diluted’ phenotype
  • co-dominance = no blending: traits appear together and remain distinct in the heterozygote
25
Q

Pleiotropy

A

Where a single gene has multiple effects on the phenotype

26
Q

polygenic inheritance

A

Where a single trait is determined by multiple genes

27
Q

Epistasis

A

When one gene masks or modifies the expression of another gene
(B is epistatic to A)
ratio of F2 in dihybrid cross = 9:3:4