Lecture 5: Chromosome Mapping Flashcards

1
Q

In Meiosis, what is the unit of transmission?

A

Chromosomes! Crossing over takes place on the arms of the chromosomes.

NOT GENES!

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2
Q

Explain Linked Genes

A
  • Can NOT undergo independent assortment
  • two or more genes located close together on the same chromosome, which means they are likely to be inherited together due to their proximity
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3
Q

Frequency of crossing over on a single chromosome is proportional to?

A

The distance between them

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4
Q

Crossing over results in?

A

RECOMBINATION

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5
Q

Define Chromosome maps

A

Indicate relative location of genes on chromosome

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6
Q

What are the 3 Meiotic Consequences

A
  1. Independent Assortment: No linkage exhibited
  2. Linkage WITHOUT crossing over: Complete Linkage
  3. Linkage WITH crossing over: Generates recombinant (crossover) gametes
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7
Q

Define Complete Linkage

A
  • No crossing over between two genes
  • Produces parental (non-crossover) gametes
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8
Q

Define Crossing over

A
  • Occurs between two non-sister chromatids
  • Both parental and recombinant (crossover) gametes are produced
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9
Q

Define Chiasmata

A
  • Synapsed chromosomes in meiosis wrap around each other
  • X shaped intersections with points of overlap
  • Points of genetic exchange
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10
Q

Percentage of offspring resulting from recombinant gametes depends on

A

distance between two genes on same chromosome

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11
Q

T/F: Two genes located close to each other along a chromosome are less likely to have chiasma

A

TRUE!!!

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12
Q

Explain Single Crossover

A
  • Occurs between two
    non-sister chromatids
  • Recombination is
    observed in 50 percent
    of gametes
  • In genes 50 map units
    apart, crossing over can
    be expected between
    100 percent of tetrads[{{type}} Annotation]
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13
Q

What is centimorgans on a gene?

A

Distance between two genes in map units

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14
Q

What are Single Crossovers used to determine?

A

Used to determine distance between two linked genes

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15
Q

Explain Double Crossover

A
  • Double exchanges of genetic material
  • Used to determine distance between three linked genes
  • Genes must be heterozygous for two alleles
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16
Q

Explain Somatic Cell Hybridization

A
  • Made possible the assigning of human genes to their respective chromosomes
  • Involves fusing two cells into a single hybrid cell: heterokaryon
17
Q

Define Synkaryon

A

Heterokaryons cultured in vivo—nuclei are fused together

18
Q

What are DNA markers?

A
  • SHORT segments of DNA with KNOWN sequence and location
  • Useful landmarks for mapping
  • Earliest examples of DNA markers
19
Q

What are RFLPs: Restriction fragment length polymorphisms?

A
  • Polymorphic sites (different lengths)
  • Generated when specific DNA sequences are recognized and cut by restriction enzymes
20
Q

What are Microsatellites?

A
  • Short repetitive sequences
  • Found throughout genome
21
Q

Explain SNPs: Single-nucleotide polymorphisms (in non-sister chromatids)

A
  • Found throughout genome
  • Used by geneticists to identify and locate related genes
  • Used to screen for diseases
    Ex.) Cystic fibrosis
    Ex.) Sickle-cell anemia with a one-base chain
22
Q

Define Cystic fibrosis

A
  • Gene located by using DNA markers
  • Life-shortening autosomal recessive exocrine disorder
  • Gene causing disorder found on chromosome 7
23
Q

Explain Sister chromatid exchanges

A
  • Reciprocal exchanges similar to crossing over
  • Between sister chromatids (crossing over is between NON-sisters)
24
Q

Explain Harlequin chromosomes

A
  • Sister chromatids involved in mitotic exchanges
  • Patch-like appearance when stained and viewed under a microscope
25
Q

Describe some agents that INDUCE chromosome damage

A
  • Viruses
  • X-rays
  • UV
  • Mutagens
  • Increase frequency of sister chromatid exchange in Bloom syndrome
26
Q

Explain Bloom syndrome

A
  • Human disorder
  • Caused by mutation in BLM gene
    chromosome 15
  • Prenatal and postnatal retardation of growth
  • Excessive SCEs
  • Many translocations
27
Q

Explain BLM gene

A
  • Encodes enzyme DNA helicase
  • DNA helicase’s known role is DNA
    replication
  • Not known how it causes Bloom Syndrome