Unit 7- Linkage, Recomb, and Eukaryotic Gene Mapping Flashcards

1
Q

Principle of Segregation

A

alleles at same locus of homologous pairs separate during meiosis

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2
Q

Indep Assortment

A

alleles at one locus sort indep from alleles at another locus

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3
Q

recombination

A

alleles sort into new combinations

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4
Q

complete linkage

A

leads to nonrecombinants
- genes very close together and no crossing over

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5
Q

crossing over with linked genes

A

leads to recombinants (at most half: a single crossover only affects 2 of 4 chromatids)

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6
Q

calc recomb freq

A

of recomb progeny/ total # of progeny x100%

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7
Q

coupling (cis config)

A

wild-type alleles are found on 1 chromo; mutant alleles are found on the other chromo
*mostly parental pheno

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8
Q

Repulsion (trans config)

A

wild-type alleles and mutant allele are found on the same chromo
* mostly recomb pheno

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9
Q

INTERchromosomal Recombination

A

crossing over between genes located on DIFFERENT chromosomes (due to indep assortment. Mendelian)

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10
Q

INTRAchromosomal Recombination

A

crossing over between genes located on the SAME chromosome

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11
Q

chi-square test of independence

A
  1. Set up table of parents and their progeny (like a punnet sq) with row/column totals
  2. calc expected: row total x column total / grand total)
  3. sum of (O-E)^2 / E
  4. d:f (# rows-1) x (# columns -1)
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12
Q

Gene mapping with recomb freqs

A
  • genetic maps determined by recomb freq (1 mu = 1%)
  • map units: centiMorgans
    (as % goes up, so does distance)
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13
Q

constructing a genetic map with the 3pt testcross

A
  • more efficient mapping technique
  • order of the 3 genes can be established in a single set of progeny
  • some double crossovers can usually be detected
  • provides more accurate map distances
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14
Q

steps in determining gene order in 3pt cross

A
  1. identify the nonrecomb progeny (2 most numerous)
  2. Identify the recomb progeny (2 least numerous)
  3. compare the pheno of double-crossover progeny with the pheno of nonrecomb progeny. (should be alike in 2 characteristics and differ in 1)
  4. differing characteristic is encoded by the middle gene
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15
Q

calc recomb freq

A

sum of all single and double crossovers/ total progeny

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16
Q

coeff of coincidence

A

of obs double crossovers/ # of expected double crossovers

17
Q

interference

A

The degree to which one crossover interferes with
additional crossovers in the same region
1 - coeff of coincidence

18
Q

Poisson distribution

A

predicts the probability of multiple rare events

19
Q

mapping techniques

A
  • mapping with molec markers (RFLPs)(variations in DNA sequence detected by cutting the DNA with
    restriction enzymes)
  • Genome-wide association studies (associations w/in pops, haplotype, and linkage disequilibrium)
20
Q

genetic markers

A

variable genes with easily observable phenos for which inheritance could be studied
- ex: lower color, seed shape, blood types, and biochemical difference

21
Q

Physical-mapping methods are used to determine the physical position of genes on particular chromo

A
  • somatic-cell hybridization
  • deletion mapping
  • physical mapping through molec anaysis (in situ hybridization)
22
Q

hetrokaryons

A

hybrid cells formed during somatic-cell hybridization (look for differing presence of chromo)

23
Q

Fluorescence in Situ Hybridization (FISH)

A

uses a single-stranded complementary DNA probe for the gene

24
Q

Recomb rates exhibit extensive variation

A
  • among species
  • among chromos of same species
  • among males and females
25
Q

Walter Sutton’s Chromo Theory of Inheritance

A

genes are physically located on chromo

26
Q

Netti Steven’s and Edmund Wilson’s

A

sex was associated with specific chromo in insects

27
Q

Calvin Bridges’

A

nondisjunction of x chromo was related to the inheritance of eye color in Drosophilia

28
Q

Harriet Creighton and Barbara McClintock

A

interchromosomal recomb was the result of physical exchange between chromos

29
Q

linkage analysis

A

based on the detection of physical linkage between genes,
as measured by the rate of recombination

30
Q

genomewide association studies

A

looks for associations between traits and alleles in a POP

31
Q

haplotype

A

A specific set of linked alleles

32
Q

linkage disequilibrium

A

nonrandom association
between alleles in a haplotype

33
Q

single-nucleotide polymorphisms
(SNPs)

A

positions in the genome where people vary in a single nucleotide base

34
Q

deletion mapping

A

homo for mutation x hetero for deletion
- if trait in deletion area, 50% recomb
- if trait isnt in area, wild-type