Linkage, Recombination & Gene Mapping Flashcards

1
Q

Interchromosomal Genetic Variation

A

Random segregation of DIFFERENT chromosomes during anaphase 1 of meiosis.

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2
Q

Intrachromosomal Genetic Variation

A

Meiotic recombination between loci on the same chromosome

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3
Q

Frequency of Germline Mutation

A

Relatively low compared to interchromosomal and intrachromosomal

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4
Q

How do you distinguish between unlinked and linked genes?

A

Using a “two point” or dihybrid testcross.

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5
Q

Dihybrid or two point cross

A

Tracks the segregation of alleles at TWO loci.

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6
Q

Monohybrid cross

A

Tracks the segregation of alleles at ONE locus.

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7
Q

For single crossovers, the frequency of recombinant gametes is half the frequency of crossing over because

A

Each crossover takes place between only two of the four chromatids of a homologous pair.

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8
Q

Calculating recombination requency

A

Recombination frequency = (No. recombinant progeny/Total No. of progeny) X 100%

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9
Q

We can use genetic data from testcrosses (in model organisms) or from preexisting pedigrees (in humans) to

A
  1. quantitatively estimate distances between loci

2. establish simple genetic maps of the entire genome of organisms - ABCD or ACBD

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10
Q

What is a centiMorgan (cM) or map unit (m.u.)?

A

a unit for measuring genetic linkage. It is defined as that distance between loci for which the recombination frequency in a single generation is 0.01or 1%.

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10
Q

What does the number of genotypes from a dihybrid cross reveal?

A

The type of alleles at each of the two loci

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10
Q

what is coupling (cis configuration)

A

wild type alleles are found on one chromosome; mutant alleles are found on the other chromosome.

  • –A——–B—
  • –a———b—
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11
Q

Repulsion (trans configuration)

A

wild type allele and mutant allele are found on the same chromosome.

  • –A———b—
  • –a———B—
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12
Q

Steps in determining gene order in a three-point cross

A
  1. identify the nonrecombinant progeny (two most-numerous phenotypes)
  2. Identify the double-crossover progeny (two least-numerous phenotypes).
  3. Compare the phenotype of double-crossover progeny with the phenotype of nonrecombinant progeny. They should be alike in two characteristics and differ in one.
  4. The characteristic that differs between the double crossover and the nonrecombinant progeny is encoded by the middle gene.
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13
Q

What is the middle locus if the resulting nonrecombinant progeny are A+B+C+ and ABC and the double crossover progeny are ABC+ and A+B+C?

A

C

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14
Q

Variation

A

generated by both interchromosomal combinations and intrachromosomal recombinations.

15
Q

Coupling and repulsion

A

refer to the arrangement of alleles at two loci on homologous chromosomes. This affects the numbers of progeny of each genotype (and phenotype) in a dihybrid testcross.