Unit 3 Mutations Flashcards

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

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
TFIID is removed
RNA polymerase II won't bind to TATA box
26
Rat1 is mutated to only have 3' to 5' exonuclease activity
extra mRNA cannot be degraded
27
the promoter sequence is moved to be 3 unites upstream of the terminator
pre-mRNA will be very short
28
a poly(U) tail was added
pre-mRNA would be degraded
29
exons and introns were switched
exons would be removed and introns translated
30
an enzyme is added to a prokaryotic cell that degrades spliceosome
nothing
31
an enzyme is added to a prokaryotic cell thar degrades spliceosome
introns would be removed
32
amino-acyl-tRNA-synthetase begins binding amino acids and tRNA randomly
codons no longer match amino acids
33
the shine-dalgarno sequence is mutated
small subunit cannot bind mRNA in prokaryotes
34
the large subunit loses its enzymatic activity
no peptide bonds
35
release factor cannot bind to the ribosome
peptide not released
36
cap binding proteins are mutated
subunits cannot bind mRNA in eukaryotes