Chapter 5 - Linkage, Recombination, Remapping

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27 Terms

1
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What is genetic linkage?

The tendency of genes located close together on the same chromosome to be inherited together.

2
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What is linkage group?

A group of genes located on the same chromosome that tend to be inherited together due to genetic linkage.

3
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What is a recombinant gamete?

A gamete that contains a new combination of alleles not found in the parent due to crossing over.

4
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What is a nonrecombinant gamete?

A gamete that carries the same combination of alleles as found in the parent (also called parental gamete).

5
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What is a recombinant progeny?

Offspring that have a different combination of traits than either parent due to recombination during meiosis.

6
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What is the recombination frequency and how is it calculated?

(number of recombinant progeny / total number of progeny) * 100%

7
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What is the maximum recombination frequency and why?

50% because crossing over between two loci can occur in up to half of all meioses.

8
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What unit is used to express distances on a genetic map?

centiMorgan (cM), where 1 cM = 1% recombination frequency.

9
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What is the difference between a genetic map and physical map?

A genetic map is based on recombination frequencies, while a physical map shows actual base pair distances between loci.

<p>A genetic map is based on recombination frequencies, while a physical map shows actual base pair distances between loci.</p>
10
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What does it mean when genes are in cis (coupling) configuration?

Wild type alleles are on one chromosome and mutant alleles are on the homologous chromosome.

11
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What does it mean when genes are in trans (repulsion)?

Each chromosome has one wild-type and one mutant allele.

12
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What is complete linkage?

A condition where genes are so close together on the chromosome that no crossing over occurs between them.

13
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Why did Mendel not observe genetic linkage in his experiments?

The genes he studied were either different chromosomes or far apart on the same chromosome, so they assorted independently.

14
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How can you test for linkage between two genes?

By performing a testcross with a double heterozygote and observing if recombinant progeny occur at frequencies lower than 50%.

15
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What is the purpose of a three-point testcross?

To map the order and distances between three genes and to detect double crossovers.

16
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Why does a two-point testcross underestimate distances between far-apart genes?

Because it fails to detect double crossovers that restore parental combination.

17
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What is incomplete linkage?

When two genes on the same chromosome undergo crossing over in some, but not all, meiotic events.

18
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How do recombination frequencies relate to physical distances on a chromosome?

Higher recombination frequencies usually indicate that genes are farther apart on the chromosome.

19
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What does a three-point testcross allow that a two-point testcross does not?

Determination of gene order and more accurate estimation of distances, including detection of double crossovers.

20
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In notation for linked genes, what does “AB/ab” represent?

A heterozygote with dominant alleles A and B on one chromosome and recessive alleles a and b on the homologous chromosome.

21
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In a complete linkage testcross, what gametes are produced by a heterozygote with genotype MD/md?

Only MD and md gametes (nonrecombinant).

22
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If only MD and md progeny are observed in a testcross involving genes M and D, what does this suggest?

The genes are completely linked and no crossing over occurred.

23
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In a cross involving incomplete linkage, which gametes would be recombinant for a heterozygote with genotype AB/ab?

Ab and aB

24
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If two genes are 20 cM apart, what proportion of gametes are expected to be recombinant?

20%

25
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Given recombination frequencies of A–B = 10%, B–C = 5%, and A–C = 15%, what is the gene order?

A – B – C

26
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In a testcross, 70 progeny are nonrecombinant (MD and md) and 30 are recombinant (Md and mD). What is the recombination frequency?

30 / (70 + 30) = 30%; recombination frequency = 30%

27
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What is the genotype of a heterozygous F₁ individual from a cross between MM DD and mm dd parents?

MD/md