Genomics I: Ch 23 Flashcards

(20 cards)

1
Q

Genomics def

A

begins with the mapping of the genome & progresses ultimately to its complete sequencing

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2
Q

Functional genomics def

A

examines how the interactions of genes produce the traits of an organism

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3
Q

Proteomics def

A

study of all the proteins encoded by the genome & their interactions

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4
Q

2 common ways to organize DNA regions:

A
  1. cytogenetic mapping: relies on microscopy; genes are mapped relative to band locations on the chromosomes
  2. linkage mapping: relies on genetic crosses; genes are mapped relative to reach other - distance computed in map units
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5
Q

describe cytogenic mapping

A

in situ hybridization can locate the position of a gene at a particular site with an intact chromosome

  • used to map location of genes or DNA sequences within large eukaryotic chromosomes
  • researchers use it to detect “target” DNA
  • most common method uses fluorescently labeled DNA probes
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6
Q

what is FISH?

A

fluorescence in situ hybridization

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7
Q

monomorphic def

A

a certain protein comes only in 1 particular formula

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8
Q

describe linkage mapping via crosses

A

relies on the frequency of recombinant offspring to map genes
- uses molecular markers ( DNA segment found at a specific site, uniquely recognized)

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9
Q

RFLP?

A

restriction fragment length polymorphs

  • restriction frags come from DNA restriction enzymes that cut the sequence
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10
Q

What molecular markers used for?

A
  • gene might cause human disease
  • can follow markers in family pedigrees
  • can be starting point to clone gene by chromosome walking
  • used to follow genes involved in quantitative traits

**most likely used for diseases

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11
Q

microsatellite def

A
  • short, repetitive sequences
  • abundantly dispersed throughout a species’ genome
  • variable in length in individuals
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12
Q

the most common human microsatellite is ___

A

(CA)n, where n = 5 - 50+

found in every 10k bases in genome

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13
Q

physical mapping requires _____

A

previous knowledge (need to have done some linkage or cytogenetic mapping)

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14
Q

STS def

A

sequence tagged site

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15
Q

what do researchers need for cloning?

A

a series of clones that contain overlapping chromosomal DNA?

this collection = contig

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16
Q

def YAC, BAC, PAC & why they’re important

A

ac = artificial chromosome
yeast, bacterial, P1

these can accept large chromo fragments (that plasmids & viral vectors cannot)

17
Q

common method used for positional cloning ______

A

chromosome walking

18
Q

what is needed in chromosome walking?

A

must know the relative position of target gene to marker

19
Q

shotgun sequencing def

A

method where small DNA fragments are randomly generated from larger pieces and sequenced.

most efficient & inexpensive way to sequence genomes

20
Q

open reading frame def

A

anything between start & stop codons

  • can start with the 1st 2nd or 3rd nucleotides
  • cannot contain stop codons