Genetic Screens Flashcards

1
Q

Forward vs Reverse

A
Forward = genes important for process
Reverse = process gene important for
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2
Q

Selection vs Screen

A
Selection = only variant survives
Screen = look for variant with phenotype
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3
Q

Non-complementation

A

Same Gene

- no synthesis of leucine

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4
Q

Complementation

A

Different Genes

- synthesis of leucine

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5
Q

Zygotic

A
  • zygote homozygous for mutation

- F3 = dead embryo

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6
Q

Maternal

A
  • mother homozygous for mutation –> normal egg

- F4 = larvae affected

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7
Q

Transformation

A

Plasmids (have selectable marker)
Random Insertion
Homologous Recombination

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8
Q

Injecting DNA

A

Random Insertions

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9
Q

Transposon Mediated Transformation

A
  • transposase cut transposon out of genome
  • transposon contains inverted repeats
  • 2 plasmids for control (1 = transposase, 2 = transposon)
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10
Q

Site Specific Recombination

A
  • use recombinase find recombination site

- duplicating recombination sites

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11
Q

Functional Complementation

A
  • DNA fragment & cdc42 lf = no complementation

- cdc42+ & cdc42 lf = complementation (growth)

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12
Q

Mutational Analysis

A
  • mutation in gene
  • which mutations complement cdc42lf allele
  • important for function
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13
Q

Misexpression

A
  • heat shock promoter express ANTP all cells
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14
Q

Knock Out Genes

A
  • homologous recombination

- interrupts gene

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15
Q

RNAi

A
  • dicer cuts into 20 nucleotide fragments
  • binds to AGO (RNA induced silencing complex)
  • binds and degrades mRNA
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16
Q

lin-14

A

lin-14 lf = advanced development L2

lin-14 gf = suppress L2 + replace with L1

17
Q

lin-4

A
  • regulates expression of lin-14

- SUPPRESS translation of lin-14 in L2

18
Q

miRNA

A
  • in genome –> pri-miRNA —> pre-miRNA
  • dicer cuts up
  • binds to AGO (RNA induced silencing complex)
  • suppress translation
  • miRNA guides RISC to specific mRNA
19
Q

RNAi Screens

A

1) insert cDNA of gene into E.coli plasmid
2) induce expression = RNA copy
3) C.elegans eat E.coli –> dsRNA absorbed
4) dsRNA diced, bind to AGO, degrades = no translation

20
Q

Restriction Modification Immunity

A

1) Restriction enzyme cuts phage DNA

2) Methylase methylates genomic DNA protect from restriction enzyme

21
Q

CRISPR (Acquire)

A

1) CAS cuts phage DNA next to PAM sequence (NGG)

2) Inject phage DNA into genomic DNA

22
Q

CRISPR (Immunity)

A

1) CRISPR array –> pre-crRNA
2) Cas9 (guide RNA + tracer RNA) made
3) Cas9 finds PAM in phage DNA
4) guide RNA unwinds dsDNA –> ds break = inactive

NO PAM = cannot cut genomic DNA

23
Q

CRISPR (Reengineered)

A

1) Cas9 (single mRNA with guide function + seq to bind)
2) Creates ds breaks

  • attach function to Cas9
  • mutations to knockout ability make ds break
  • find and bind to unique sequences in genome