Transcription Regulation of gene Flashcards

1
Q

although the mechanism of
transcription in bacteria and
eukaryotes is fundamentally similar,
transcription is substantially more
complicated in Blank

A

eukaryote

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2
Q

one significant difference is that the
DNA of eukaryotes (and Archaea) is
wrapped around Blank to form
nucleosomes, and the nucleosomes
are further organized into Blank

A

Histones, chromatin

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3
Q

nucleosomes represses

A

gene
expression

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4
Q

only those Blank by
specific positive regulatory
mechanisms are transcribed

A

genes activated

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5
Q

large, complex multimeric proteins
(500 to 700 kDa), consisting of Blank or
more types of subunit

A

10

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6
Q
  • localized to the nucleolus
  • transcribes the major rRNA genes
A

RNA polymerase I

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7
Q
  • transcribes most noncoding RNA
    genes and all protein-encoding genes
  • responsible for the synthesis of mRNA
A

RNA polymerase II

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8
Q
  • transcribes tRNA genes, the rRNA
    genes encoding 5S rRNA, and a variety
    of other small RNAs, including several
    involved in mRNA processing and
    protein transport
A

RNA polymerase III

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9
Q

all possess 2 large subunits (each 140
kDa or greater) having sequence
similarity to the large Blank and Blank
subunits of E. coli RNA polymerase

A

β- and β’

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10
Q

the 3 classes of RNA polymerase
can be distinguished by their
sensitivity to

A

a-amanitin

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11
Q
  • a bicyclic octapeptide produced by
    the poisonous mushroom Amanita
    phalloides (destroying angel
    mushroom)
  • blocks RNA chain elongation
A

a-amanitin

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12
Q

RNA polymerase I is Blank to this
compound, RNA polymerase II is
Blank and RNA polymerase
III is Blank

A

resistant, very sensitive, less sensitive

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13
Q
  • DNA binding proteins that
    recognize and accurately initiate
    transcription at specific promoter
    sequences
  • RNA polymerase I templates are
    the rRNA genes
A

transcription factors

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14
Q
  • RNA polymerase III interacts with
    transcription factors Blank, Blank, Blank
A

TFIIIA, TFIIIB, TFIIIC

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14
Q
  • must carry out its function at any
    moment only on those genes whose
    products are appropriate to the
    needs of the cell in its ever-changing
    metabolism and growth
A

RNA polymerase II

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15
Q

both yeast and human RNA
polymerase II consist of Blank different
polypeptide

A

12

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16
Q
  • essential to RNA polymerase II
    function
A

C-terminal domain (CTD)

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17
Q

True or False
only RNA polymerase III whose CTD
is not phosphorylated can initiate
transcription

A

False: RNA polymerase II

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18
Q

proceeds only after protein phosphorylation
within the CTD

A

transcription elongation

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19
Q

triggers the conversion of an initiation complex
into an elongation complex

A

phosphorylation

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20
Q

also plays a prominent role in
orchestrating subsequent events in
the transcription process

A

CTD

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21
Q

4 stages of transcription in eukaryotes

A
  • promoter recognition and RNA
    polymerase II binding
  • initiation
  • elongation
  • termination
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21
Q

in eukaryotes, metabolic activity,
cell division, complex patterns of
embryonic development and cell
differentiation must be coordinated
through the regulation of Blank

A

gene
expression

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22
Q

all this coordinated regulation takes
place in Blank with a large quantity
and sequence diversity of DNA

A

cells

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23
a typical mammalian cell has Blank as much DNA as an E. coli cell
1500 x
24
gene expression in eukaryotes is precisely regulated in a blank and blank
time-specific and cell-specific fashion
25
* proteins that bind to specific CREs
transacting factors
26
over Blank gene-specific transacting factors are known
1600
27
* at or near the transcription start site (TSS, the nucleotide where transcription begins) * many thousands of base pairs away (distal CREs which include enhancers, insulators, silencers)
Locations of CREs
28
2 distinct CRE sequences in which efficient transcription of a protein coding gene by RNA pol II depends
* promoters (sequences at or near the TSS) * enhancers or silencers (more distantly located)
28
the promoters of eukaryotic protein-encoding genes are quite Blank and blank
complex and variable
29
* their location is defined by the core promoter, Blank to blank DNA sequence within which lies the TSS
a 50- to 100-bp
30
the assembled apparatus is megadaltons in size and occupies more than Blank bp around the TSS
100
31
about half of the core promoters for human protein-coding genes have an Inr element, about Blank have a TATA box
20%
32
* has the consensus sequence: C/G/T C/G/T- C-A-C/G/T-A/T, with the bold A at position +1, defining the TSS * found in housekeeping genes
Inr element
33
is usually located at position −31 from the TSS * a feature of tissue-specific genes
TATA box (consensus sequence T-A T-A-A-T/A-A/T-A/G)
34
the Blank nature of the TATA box facilitates promoter melting and access of the transcription apparatus to the template strand
A:T-rich
35
* embedded in the coding region, positioned at +28 to +33 relative to the TSS
DPEs
36
* genes that encode proteins commonly present in all cells and essential to normal function * transcribed at more-or-less steady levels → constitutive expression
housekeeping genes
37
short nucleotide sequences called Blank found near the promoter (the promoter proximal region)
response elements (REs)
38
* CREs located quite distant from the genes they regulate, ranging from several kbp to nearly a megabase pair in some human genes
enhancers and silencers
39
* has a highly variable DNA sequence less than 100-bp-long * located in a region of chromatin accessible to DNA-binding proteins because nucleosomes are sparse
enhancer
40
(ENCODE) meaning
Encyclopedia of DNA Elements
40
* sequences where transcriptional repressors bind * searches through the human genome by the Encyclopedia of DNA Elements (ENCODE) Consortium reveal hundreds of thousands of putative enhancers and silencers, far more than the number of protein-coding gene
silencers
41
* called upstream activation sequences (UASs) in yeast * assist transcription initiation
enhancers
42
43
* sequences are bidirectional * can be removed and then reinserted in the reverse sequence orientation without impairing their function * represent modules of consensus sequence * non-specific * stimulate transcription from any promoter that happens to be in their vicinity * function is dependent on recognition by a specific transcription factor
enhancers
44
* DNA sequences of 0.1–1 kb that act in 2 ways ✓ to shield regions of chromatin active in transcription from inactive regions ✓ to block an enhancer from stimulating transcription from a specific promoter
insulators
45
True or False an insulator sequence cannot act as an enhancer blocker if it is located somewhere along the DNA sequence between the enhancer and the promoter
False: can act
46
is a tumor response element activated in the presence of tumor-promoting phorbol esters such as TPA (tetradecanoyl phorbol acetate)
TRE
47
* a metal binding protein that protects cells against metal toxicity by binding excess amounts of heavy metals and removing them from the cell * always present at low levels * its concentration increases in response to heavy metal ions such as cadmium or in response to glucocorticoid hormones
metallothionein
48
when MTF binds heavy metals such as blank and blank, it activates metallothionein gene expression by binding to the MREs
cadmium and zinc
49
in the presence of the stress hormone cortisol, Blank binds to the metallothionein gene GRE, activating transcription *
growth hormone (GR)
50
nearly Blank of human genes have a GRE
30%
51
* composed of more than 100 polypeptides * RNA polymerase II * a set of general transcription factors (TFIIA, TFIIB, TFIID, TFIIE, TFIIF, TFIIH) * Mediator, a 1.5-megadalton complex that mediates interactions between RNA pol II and proteins bound at distal CREs
PIC (preinitiation complex)
52
consists of the TBP (the TATA binding protein), which directly recognizes the TATA box within the core promoter and a set of TBP associated factors (TAFs)
TFIID
53
* the first GTF to recognize and bind to the promoter
TFIID complex
54
* the TATA box-binding protein that recognizes the promoter core, making contacts with the DNA minor groove and distorting and bending the DNA so that sequences upstream and downstream of the TAT box come into closer proximity
TBP
55
* stimulates transcription by stabilizing the interaction of TFIID and the TATA box
TFIIA
56
* serves as a bridge between promoter-bound TFIID and RNA pol II, positioning the RNA polymerase active site over the promoter
TFIIB
57
* the assemblage of RNA polymerase II and these other proteins at the promoter
initiation complex
58
transcription initiation in eukaryotes also requires Mediator, which in humans is composed of Blank subunits, the Med proteins
26
59
* a megacomplex of about 20 proteins * named for its Spt, Ada, and Gen5 subunits
SAGA
60
* a family of proteins involved in gene expression
Spt
61
* a histone acetyltransferase (HAT, a histone-modifying enzyme)
Ada
62
* a lysine acetyltransferase (KAT)
Gen5
63
* contains TAF (TBP-associated proteins) subunits * can recognize TATA boxes * required for the expression of most RNA pol II-transcribed genes
SAGA
64
is critical for recognition, with AA side chains providing most of the critical contacts with DNA
hydrogen bonding
65
protein contacts with the bases of DNA usually occur within the Blank (but not always)
major groove
66
3 kinds of small, distinctive structural motifs
* helix-turn-helix (HTH) * zinc finger (Zn-finger) * leucine zipper-basic region (bZIP)
67
* occurs on DNA in the nucleus
transcription
68
* occurs on ribosomes in the cytoplasm
translation
69
*must be transported from the nucleus to the cytosol to be translated
transcripts
70
* alterations that convert the newly synthesized RNAs, or primary transcripts, into mature mRNAs * eukaryotic mRNAs are exclusively monocistronic
processing
71
* protein-coding regions of an interrupted or split gene * sequences that are represented in mature RNA molecules
exons
72
* non coding regions * intervening nucleotide sequences that are removed from the primary transcript when it is processed into a mature RNA
introns
73
* adding a GMP to the 5’-phosphate end
capping
74
* addition of methyl groups on various bases and riboses at the 5’-end
methylation
75
* addition of multiple A residues to the 3’-end
polyadenylylation
76
* removal of all introns
splicing
77
* primary transcripts or pre-mRNAs that serve as precursors to mRNA * shortly after transcription of hnRNA is initiated, the 5’-end of the growing transcript is capped by addition of a guanylyl residue
heterogeneous nuclear RNA (hnRNA)
78