Gene Expression Flashcards

(57 cards)

1
Q
  • is the process wherein genetic information from DNA is transferred into RNA.
  • It is the first step in the expression of the
    genetic information stored in the genome:
    from gene to gene product (frequently a
    protein).
A

Transcription

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2
Q

It became very rapidly clear in the 50s that
DNA could not be directly converted into
protein, and there had to be an intermediate
step.
● This unstable product was identified as

A

RNA

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3
Q

● It is a single-stranded molecule that
contains Uracil instead of Thymine.
● It uses ribose sugar instead of
deoxyribose

A

RNA

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4
Q

Three major classes of RNA:
They participate in protein synthesis and are synthesized from DNA by transcription

A
  1. Ribosomal RNA, rRNA
  2. Transfer RNA, tRNA
  3. Messenger RNA, mRNA
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5
Q

Other forms of RNA:

A
  • small nuclear RNA (snRNA).
  • small nucleolar RNA (snoRNA).
  • microRNA (miRNA). ~22 nt RNA molecules that regulate the expression of mRNA molecules.
  • long non-coding RNA (lncRNA).
  • siRNA – RNA interference&raquo_space;> 2006 Nobel Prize Andrew Z. Fire & Craig C. Mello
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6
Q

(snRNA).

A

small nuclear RNA

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7
Q

(snoRNA).

A

small nucleolar RNA

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8
Q

(miRNA). ~22 nt RNA molecules that regulate the expression of mRNA molecules.

A

microRNA

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9
Q

(lncRNA).

A

long non-coding RNA

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10
Q

siRNA –&raquo_space;> 2006 Nobel Prize Andrew Z. Fire & Craig C. Mello

A

RNA interference

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11
Q

is a segment (or segments) of the DNA with a distinct
sequence of nucleotides that is transcribed and translated into a
protein product that contributes to the expression of a specific
phenotype/function

A

gene

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12
Q

The sequences after the transcription initiation site towards the 3’ end of the template strand are called

A

upstream elements

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13
Q

while those sequences before the transcription termination site towards the 5’ end are
called the

A

downstream elements

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14
Q

The CORE enzyme has five subunits (~400 kDa)

A

β’, β, α, αCTD, ω

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15
Q

: largest subunit, encoded by rpoC.
Contains part of the active center responsible for RNA synthesis

A

β’

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16
Q

: second-largest subunit, encoded by rpoB.
Contains the rest of the active center responsible for RNA synthesis.

A

β

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17
Q

: third-largest subunit and is present in two copies per molecule of
RNA pol, αI and αII. Each α contains two domains: αNTD (N-Terminal
domain) and αCTD (C-terminal domain). αNTD required for assembly
of RNA pol

A

α

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18
Q

required for interaction with the promoter, non-sequence/non
specific interactions at most promoters and sequence-specific
interactions at upstream-element-containing promoters. α interacts
with regulatory factors.

A

αCTD

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19
Q

: smallest subunit. ω facilitates assembly of RNAP and stabilizes
RNAP

A

ω

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20
Q

TREU OR FALSE
RNA polymerases in some living organisms
are evolutionary relate

A

False: all

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21
Q

EVENTS IN TRSNCRIPTION:
the RNA polymerase, together with any
initiation factors required, binds to the promoter, the DNA
sequence where transcription starts.
● Once formed, the promoter-polymerase complex
undergoes structural changes required for initiation to
proceed.
● The DNA will then unwind around the point where
transcription will start.
● The base pairs are disrupted, producing a “transcription
bubble” of single-stranded DNA.
● The new ribonucleotide is added to the 3’ end of the
growing strand since transcription always occurs in a 5’
to-3’ direction.

A

Initiation

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22
Q

TRUE OR FALSE
Only one RNA strand acts as a template on which the RNA strand is built.

A

False: DNA

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23
Q

This strand is called the template strand or
?

A

antisense strand or non-coding strand.

24
Q

The other strand to where the code being copied is located is called the non-template strand or?

A

the sense strand or the coding strand.

25
The -10 region is located 10 nucleotide (nt) upstream of the transcription start site and is known as the Blank
Pribnow-Schaller box.
26
The -35 region is located at 35 nt upstream of the transcription start site. ● Many prokaryotes share a common or similar sequence at their -35 and -10 regions. ● These shared sequences are called Blank
consensus sequences.
27
At -25 is the sequence Blank
TATA (TATA box)
28
at -80 is the sequence Blank
CAAT (CAAT box)
29
In prokaryotes, the initiation factor is called the Blank
sigma factor/s
30
In eukaryotes, the initiation factor is called a Blank.
transcription factor (TF)
31
True or False TATA-binding protein is also part of TFIIA that binds the TATA-box.
False: TFIID
32
During Blank, the enzyme performs an impressive range of tasks in addition to the catalysis of mRNA synthesis. ● It unwinds the DNA in front and reanneals it behind, it dissociates the growing mRNA chain from the template as it moves along, and it performs proofreading functions. ● Recall that during replication, in contrast, several different enzymes are required to catalyze a similar range of functions.
elongation
33
● Once the polymerase has finished transcribing the protein-coding region or the gene, it must stop and release the mRNA product as well as dissociate from the DNA. ● In some cells, specific and well characterized sequences signal termination of transcription. ● In others, it is less clear what triggers the enzyme to stop transcribing and detaching itself from the template.
Termination
34
occurs when the termination sequence forms a GC stem-loop in the nascent RNA, which causes RNA pol to pause.
Rho-independent termination
35
the "hot pursuit" model for rho action suggests that Rho binds to a nascent RNA chain
Rho-dependent termination
36
37
This process involves the addition of a modified guanine base to the 5’ end of the RNA.
Capping
38
A Blank is added to the 5' end of the growing transcript by a 5'-to-5' phosphate linkage.
7-methylguanosine cap
39
Unlike prokaryotes, eukaryotic genes have noncoding DNA sequences called Blank inserted between the coding sequences called Blank.
introns, exons
40
Thus, the final stage of RNA processing after the termination of transcription is the removal of introns (noncoding sequences) and joining of the exons (coding sequences) together. ● This process is called Blank
splicing
41
* occurs in introns that form a ribozyme, performing the functions of the spliceosome by RNA alone
Self-splicing
41
This process is called splicing which is carried out in a series of reactions catalyzed by the Blank, a ribonucleoprotein complex.
spliceosome
42
* occurs within same pre-mRNA molecule
Cis-splicing
43
* uses two separate pre-mRNA molecules to form a chimeric non-colinear RNA
Trans-splicing
44
Single-stranded RNA that is complementary to a mRNA transcribed within a cell. * These are long noncoding RNA (lncRNA).
Antisense RNA
45
True or False This effect could occur in trans. i.e. the antisense RNA needs to be produced from the same gene as the sense RNA.
False: does not need
46
Won the Nobel Prize in Physiology or Medicine 2006 for their discovery of RNA interference gene silencing by double-stranded RNA
Andrew Z. Fire and Craig C. Mello
47
True or False The RNAi process is Found in eukaryotes and prokaryotes.
False: only found in eukaryotes.
48
True or False Canonical RNAi is triggered by some form of short dsRNA.
False: long dsRNA.
49
can originate from various sources including viruses and their replication intermediates or base pairing if RNAs transcribed in the genome (either as an intramolecular duplex (hairpin dsRNA), or by base pairing RNAs transcribed in cis (convergent transcription) or in trans (from interspersed elements, pseudogenes etc.).
dsRNA
50
– where one strand of siRNA duplex is selected and loaded onto an Argonaute
loading
51
– cleavage of long dsRNA into siRNA duplexes by RNase III Dicer
dicing
52
protein from AGO subfamily
Argonaute
53
True or False In all species, RNAi also involves an RNA-dependent RNA polymerase (RdRp), which may generate initial substrates or participate in amplification of the response by converting cognate RNAs into dsRNA.
False: some species
54
Won the Nobel Prize in Physiology or Medicine 2024 for the discovery of microRNA and its role in post-transcriptional gene regulation
Victor Ambros and Gary Ruvkun
55
True or False miRNAs are genome-encoded.
True
56
The key bridge between AGO and proteins mediating deadenylation and decapping is Blank.
GW182 protein