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

(34 cards)

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
Walter Sutton's Chromo Theory of Inheritance
genes are physically located on chromo
26
Netti Steven's and Edmund Wilson's
sex was associated with specific chromo in insects
27
Calvin Bridges'
nondisjunction of x chromo was related to the inheritance of eye color in Drosophilia
28
Harriet Creighton and Barbara McClintock
interchromosomal recomb was the result of physical exchange between chromos
29
linkage analysis
based on the detection of physical linkage between genes, as measured by the rate of recombination
30
genomewide association studies
looks for associations between traits and alleles in a POP
31
haplotype
A specific set of linked alleles
32
linkage disequilibrium
nonrandom association between alleles in a haplotype
33
single-nucleotide polymorphisms (SNPs)
positions in the genome where people vary in a single nucleotide base
34
deletion mapping
homo for mutation x hetero for deletion - if trait in deletion area, 50% recomb - if trait isnt in area, wild-type