Lecture 2 Flashcards

1
Q

What 4 processes contribute to genetic variation?

A

Mutation.
Independent assortment.
Crossing-over.
Random fertilisation.

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2
Q

What are the number of possible offspring combinations from one couple?

A

2^46.

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3
Q

What is a recombinant phenotype?

A

The combination of phenotypes differs from that found in either parent.

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4
Q

2 ways recombinant phenotypes can occur?

A

Independent assortment.

Crossing over.

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5
Q

What is crossing over?

A

Process of genetic recombination that gives rise to new combinations of linked genes.

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6
Q

When does crossing over occur?

A

Pachytene phase of prophase I.

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7
Q

Crossing over begins with synapsis. What is this?

A

Pairing of homologous chromosomes.

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8
Q

What is the synaptonemal complex?

A

Protein zipper that holds homologous chromosomes together in the tetrad.

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9
Q

What does the synaptonemal complex lead to?

A

Crossing over between homologous chromosomes.

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10
Q

What is the result of crossing over?

A

Recombinant chromosomes with new combinations of linked genes.

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11
Q

What is recombination frequency?

A

Percentage of progeny that inherit a combination of alleles that differs from either parent.

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12
Q

How do you calculate recombination frequency?

A

(No. of recombinants/Total no. of progeny)*100.

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13
Q

How can recombination frequencies be estimated?

A

Studying results of a testcross.

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14
Q

What does the recombination frequency depend on?

What will the recombinant frequency be for genes on different chromosomes?

A

Whether the genes are on same or different chromosomes.

50%.

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15
Q

Who was the first to observe gene lineage, and in what scenario?

A

T.H.Morgan.

Vestigial Wing mutant of Drosophila melanogaster.

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16
Q

How is a wild type (normal) allele usually represented?

A

Superscript +.

17
Q

What did A.H. Sturtevant notice in 1913?

A

Recombination frequency between two genes should be related to distance apart on chromosomes.

18
Q

What does 1% recombination frequency equal when creating recombination maps?

A

1cM - 1 centimorgan.

19
Q

Why do map distances not add up in multiple crossovers? (3)

A

Lead to underestimate of distance between two loci.
Mean recombination frequencies >50% are not possible.
Genes far apart on same chromosome appear to assort independently.

20
Q

What do the largest and smallest numbers indicate in a 3 point cross?

A
Largest = parental types.
Smallest = result of a double crossover.
21
Q

What are the 2 possible arrangements of alleles in a double heterozygote?
Will these affect the outcome of a testcross with the double mutant?

A

Coupling heterozygote.
Repulsion heterozygote.
Will affect testcross outcome with double mutant.

22
Q

6 instances of deviations from Mendelian ratios?

A
Sex-linkage,
Incomplete dominance,
Co-dominance.
Pleiotropy,
Polygenic inheritance,
Epistasis.
23
Q

What are autosomes?

A

Chromosomes that aren’t sex chromosomes.

24
Q

What does the Y chromosome lack in Drosophila, and what does this mean for the amount of alleles required for a male fruit fly to have white eyes?

A

Only needs one copy of XW.

25
Q

What is incomplete dominance?

A

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

26
Q

What is an example of incomplete dominance in humans?

A

Familial Hypercholesterolaemia.

27
Q

What is co-dominance? Example?

A

Where each allele affects the phenotype in separate, distinguishable ways.
ABO blood type in humans. IA and IB co-dominant.

28
Q

What is Pleiotropy?

A

When a single gene has multiple effects on the phenotype.

29
Q

What is polygenic inheritance?

A

When a single trait is determined by multiple genes.

30
Q

What is an observable trait of polygenic inheritance?

A

Trait shows continuous variation in the population.

31
Q

What is epistasis?

A

When one gene masks or modifies the expression of another gene.