chapter 30 RNA synthesis and processing Flashcards

1
Q

the catalytic site of RNA polymerase contain how many metal ions? their functions and placement?
Which aminoacids interact with them

A

2 -metal ions
one of them remain tightly bound to the enzyme
One comes in and leaves with pyrophosphate
three aspartat amino acids

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2
Q

where do RNA-polymerisation reactions take place? and how many base pairs are they?

A

transcription bubble

17 base pairs

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3
Q

what are sense + and antisense - strands?

A

sense is the coding strand

while antisense is the template strand

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4
Q

Most newly synthesized RNA-chains have ….. at their ….end

A

pppG or pppA at 5’end

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5
Q

What forces the separation of RNA-DNA hybrid after the transcription is complete

A

A structure in RNA-polymerase

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6
Q

what mechanism is used by RNA-polymerases to correct errors? the error is

A

back-tracking, in in 10^4 to 10^5

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7
Q

which subunit in RNA-polymerase holoenzyme helps recognise the promoter sequences

A

sigma subunit. RNA-polymerase bind DNA but very weakly and until the sigma unit finds the proper promoter sites

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8
Q

what are the two common promoters found in bacteria

A

TTGACA (-35)

TATAAT (-10)

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9
Q

The region containing the two common motifs in RNA-transcription initiation is called?

A

core promoter

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10
Q

strong promoter and weak promoter

A

don’t have many substitutions => frequent transcription

many subsitutation => attenuated transcription

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11
Q

When is sigma unit released

A

is released when 9-10 nucleotides are produced

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12
Q

How many sigma factors does e.coli have

A

7

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13
Q

closed and open promoter complexes
how many basepairs
how is DNA distorted

A

double helical DNA
Separated DNA-strands
17 basepairs
by being wrapped around RNA-polymerase

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14
Q

What signals termination in RNA-transcription in bacteria

at which end

A

A palindromic sequence of GC-rich area + AT-rich followed by a series of U-residues
The RNA-DNA hybrid is unstable because of the hairpin that disociate from the polymerase and cause the polymerase to dissociate from the DNA.
3’ end

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15
Q

riboswitches

A

messenger RNAs senstive to certain metabolites.

High concentration of the metabolite => more stability of hairpin => Terminator structure is formed

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16
Q

what is of the function of rho-protein in bacteria?

how does it function

A

terminate RNA-transcription. Detects termination signals that are not recognised by RNA-polymerase alone. It is a DNA-RNA helicase.
Pursues RNA polymerase until it catches it in the transcription bubble. Hydrolyses ATP in the presence of single stranded RNA

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17
Q

What is the common feature of protein-dependent and protein independent termination in RNA-transcription

A

Termination signals lie in the synthesised RNA rather than the DNA-template.

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18
Q

name some antibiotics that can inhibit transcription

A

Rifampicin and actinomycin D.

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19
Q

the function of rifampicin

A

inhibit RNA-transcription in bacteria
specifically, the initiation of RNA-synthesis
by blocking the channel into which RNA-DNA hybrid must pass

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20
Q

function of actinomycin D in both eukaryotes and prokaryotes

A

binds to double helical DNA and prevents it separation through an intercalation by the phenoxazone ring.

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21
Q

what enzymes trim and modify the precursors of tRNA and rRNA

22
Q

the function of RNase P in e.coli

A

ribonuclease P generates the correct 5’ terminal of tRNAs

23
Q

Ribonuclease III (RNase III)

A

excises 5s, 16s and 23s from primary transcripts by cleaving double-helical hairpin regions at specific sites

24
Q

The RNA-polymerase CCA adding enzyme

A

Does not require A DNA-template

25
Types of polymerases in eukaryotes table (30.2) page 997
3 types
26
what does the polymeras II carboxyl terminal containn | And it is strongly inhibited by?
CTD and it contains repeats of YSPTSPS | alpha-amanitin
27
where is TATA-box locatedd
between -30 and -100
28
When and where is DPE normally found?
when there is no TATA box between +28 and +32
29
where is the initiator element found
-3 and +5
30
differences between CAAT and GC box (location) and -35 prokaryotes in terms of position on antisense or sense strands?
CAAT and GC (-40 and -150) can be effective when present on template strand but -35 region has to be on the coding strand
31
The basal transcription apparatus
TFII complex +RNA polymerase
32
The basal transcription apparatus
TFII complex +RNA polymerase
33
The transcription process transitions from inititation to elongation in eukaryotes?
by TFIIH that phosphorylates CTD of RNA polymerase II
34
The activity of promoters in eukaryotes is increased by ....
enhancers (cis-acting elements) and they are no promoters
35
how is heat shock transcription factor different to sigma subunits in bacteria
HSTF bind directly to promoters rather than first binding response elements
36
tRNA and rRNA have ....Caps
No
37
How is poly (A) tail synthesized?
By cleavage conducted by endonucleases that recognise the sequence AAUAAA. Does not take place if 20 nucleotides are removed from its 3'side
38
MicroRNAs come from RNA polymerase
II and in some cases III as well
39
Which protein family does MicroRNA end up in?
Argonaute family. MicroRNAs guide the Argonaute to the genes to be regulated
40
RNA-editiing
Changing the sequence without changing
41
RNA-editiing
Changing the sequence without splicing
42
The introns begin with and end with....
GU and AG
43
Where is the polypyrimidin tract found and how long is it
at 3 ' end, 10 pyrimidines, followed by N and C
44
The associatio of which complexes require ATP hydrolysis in RNA-splicing
U2 and when the pre assembled complex U4-U5-U6 joins the U2 and U1, mRNA and splicing factors to form spliceosomes
45
which RNAs are released with intron lariates
U2, U5 and U6
46
What are the processes of transcription and splicing of RNA coordinated by?
By CTD of polymerase II
47
The function of RNA helicases in splicing
ATP powered to unwind RNA duplex intermediates that facilitate catalysis and induce the release of mRNPs from the mRNA.
48
Group I introns
not found in vetebrates. Self splicing that requires guanosine cofactors (GMP, GDP and GTP)
49
Group I introns
not found in vetebrates. Self splicing that requires guanosine cofactors (GMP, GDP and GTP)
50
Group 1 and group 2 self-splicing are mediated by
1: guanosine cofactors 2: 2'-OH in an adenylate residue
51
Differences between group II self-splicing introns and the spliceosome splicing of mRNA
Both use an 2'OH in an adenylate rather a guanosine factor + the intron is released as a lariat and in some cases the introns are transcribed in pieces assembling later on
52
the RNA-DNA helix? how many base pairs?
Between newly synthesized RNA and DNA-template | 8 base pairs