C2 use of polymorphisms in mapping Flashcards

1
Q

what is linkage a measure of

A

how far apart genes are from each other

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2
Q

what is linkage

A

how likely a meiotic recombination event is between 2 loci

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3
Q

what did RFLPs, DNA seq, gel electrophoresis/southern blotting, PCR allow

A

polymorphisms without corresponding traits/phenotypes to be used as genetic markers

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4
Q

are the alleles of 2 microsatellite loci always inherited together, mostly together, or 50/50 chance
what does this indicate

A

complete linkage
partial linkage
no linkage

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5
Q

what is partial linkage

A

meiotic recombination (croos-over) between M1 and M2
frequency of recombinants proportional to physical distance apart

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5
Q

what is partial linkage

A

meiotic recombination (cross-over) between M1 and M2
frequency of recombinants proportional to physical distance apart

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6
Q

what is no linkage (unlinked)

A

independently segregating, inheritance of one allele at one locus has no influence on an allele at other locus

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7
Q

in terms of linkage what does phase mean

A

on the same chr

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8
Q

in terms of linkage what does haplotype mean

A

order of in-phase alleles along chr

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9
Q

what are linkage maps based on

A

frequency of marker separation during meiosis through generations

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10
Q

what is the engine of the linkage map study

A

meiotic recombination

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11
Q

units of linkage measurement

A

human genome - cM (centimorgan)
1cM= recombination fraction of 1/100 meioses
(physcially eqvn to between 0.7 and 1 Mb of DNA)

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12
Q

what human disorders were located by linkage

A

cystic fibrosis
huntingtons
breast cancer

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13
Q

genetic map problems for disease gene identification and human genome seq

A

-genetic mapping is a mathematical exercise
-only provides a rough idea of where markers are and where disease gene is located

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14
Q

how do you collate, organise and distribute huge quantities of DNA to make a physical map

A

-a library
(storage/duplication/distribution)
-a database
(relationships)

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15
Q

why do we need to clone DNA into genomic libraries

A

a whole genome is too big and complex- limited in quantity
libraries offer infinite ‘photocopies’ (clones) of any bit of the genome

16
Q

how is DNA cloned into library

A

DNA strands chopped up and stored to make a genomic DNA library

17
Q

what do natural bacteria sometimes carry on plasmids/episomes

A

genetic material

18
Q

molecular biologists can engineer the plasmids to do what

A

carry bits of foreign DNA of interest

19
Q

what happens to the engineered bacteria and why do scientists need them

A

bacteria become photocopies; producing infinite quantities of identical (cloned) copies of that DNA
needed for analysis

20
Q

what is the restriction enzyme used to cut DNA at specific seq in genetic engineering

A

EcoRI

21
Q

in genetic engineering what is the specific sequence that DNA is cut at

A

GAATTC

22
Q

after DNA is cut in genetic engineering what happens

A

the cut ends have overhangs which allows them to reform in the presence of ligase

23
Q

5 stages of making a DNA clone library summary

A
  1. human genomic DNA broken down
  2. fragments placed in vector
  3. stored in bacteria or yeast as a clone library (BACs, YACs)
  4. single bacterium with one BAC in it will grow into a clonal pop/colony
  5. (libraries can be made from mRNA in tissue, convert to cDNA)
24
Q

what is used as probes for FISH and what does it tell is

A

BAC/YAC clones
where they are located on which chr

25
Q

what is the term given to clones that overlap

A

chr walking

26
Q

what is a contig

A

a virtual stretch of genomic DNA made up from the analysis of multiple overlapping DNA clones
contiguous

27
Q

eventually the complete genome can be reconstructed in what

A

clones

28
Q

now have access to the precise chromosomal DNA that…

A

-contains a gene associated with a particular genetic disorder
-is a convenient unit of the human genome that can be sequenced