Unit 3 Mutations Flashcards

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1
Q

H1 is degraded

A

DNA would fall off the histone

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2
Q

The phosphate group in DNA is replaced with a negative oxygen group

A

no charge

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3
Q

The phosphate group in DNA is replaced with a positive nitrogen group

A

DNA would repel histone

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4
Q

Histone proteins have a neutral charge

A

DNA and histone would be loosely bound

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5
Q

Histone proteins have a negative charge

A

histones would repel DNA

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6
Q

Histone proteins have a very positive charge

A

DNA and histones would bind tightly

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7
Q

single-strand binding proteins are degraded

A

hairpins

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8
Q

helicase is deactivated

A

replication

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9
Q

topoisomerase/gyrase is functioning slower than usual

A

DNA would replicate more slowly

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10
Q

helicase stops working halfway through replication

A

replication bubble cannot continue

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11
Q

primase is not functional

A

there will only be on the DNA

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12
Q

DNA polymerase III is degraded

A

only primers will be on the DNA

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13
Q

DNA polymerase I can no longer bind to DNA

A

there will be a mix of DNA and RNA

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14
Q

DNA polymerase delta is working extremely fast

A

lagging strand is being formed quickly

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15
Q

DNA polymerase III no longer has 3’ to 5’ exonuclease activity

A

errors cannot be fixed and replication may not continue

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16
Q

DNA polymerase I can not do 5’ to 3’ exonuclease activity

A

there will be a mix of DNA and RNA

17
Q

DNA polymerase III doesn’t have 5’ to 3’ exonuclease activity

A

no effect

18
Q

DNA polymerase alpha is mutated to remove primase activity

A

DNA replication cannot happen

19
Q

DNA polymerase III cannot perform 5’ to 3’ polymerase activity

A

primers will be removed and not replicated

20
Q

the rut sequence is mutated

A

who will not bind, RNA polymerase cannot be removed

21
Q

RNA polymerase cannot break hydrogen bonds

A

mRNA cannot be built

22
Q

rho factor loses helicase activity

A

rho factor can bind out but can’t detach RNA polymerase

23
Q

the activate site of RNA polymerase can only bind to dNTP’s

A

single stranded DNA will be made

24
Q

an enzyme degrades all transcriptional activator proteins (TAP’s)

A

transcription slows down

25
Q

TFIID is removed

A

RNA polymerase II won’t bind to TATA box

26
Q

Rat1 is mutated to only have 3’ to 5’ exonuclease activity

A

extra mRNA cannot be degraded

27
Q

the promoter sequence is moved to be 3 unites upstream of the terminator

A

pre-mRNA will be very short

28
Q

a poly(U) tail was added

A

pre-mRNA would be degraded

29
Q

exons and introns were switched

A

exons would be removed and introns translated

30
Q

an enzyme is added to a prokaryotic cell that degrades spliceosome

A

nothing

31
Q

an enzyme is added to a prokaryotic cell thar degrades spliceosome

A

introns would be removed

32
Q

amino-acyl-tRNA-synthetase begins binding amino acids and tRNA randomly

A

codons no longer match amino acids

33
Q

the shine-dalgarno sequence is mutated

A

small subunit cannot bind mRNA in prokaryotes

34
Q

the large subunit loses its enzymatic activity

A

no peptide bonds

35
Q

release factor cannot bind to the ribosome

A

peptide not released

36
Q

cap binding proteins are mutated

A

subunits cannot bind mRNA in eukaryotes