2.3 micro Flashcards

(55 cards)

1
Q

DNA-binding proteins act as

A

transcription factors to regulate transcription by turning it ON or OFF

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2
Q

Activator proteins turn transcription ON when

A

bound to activator binding sites upstream of the promoter

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3
Q

What do activator proteins help recruit?

A

RNA polymerase to the promoter

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4
Q

Repressor proteins

A

Turn transcription OFF when bound to operator sites downstream of the promoter

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5
Q

What do repressor proteins form a physical block around?

A

RNA polymerase advancements down the operon

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6
Q
A
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7
Q

The ability of activator and repressor proteins to bind DNA is controlled by small molecules called

A

effectors

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8
Q

Inducers

A

are effectors that result in turning transcription ON. When bound to activator proteins, they
facilitate the activator’s binding to the activator binding site. When bound to repressor proteins, they
prevent the repressor’s binding to the operator.

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9
Q

Corepressors

A

are effectors that result in turning transcription OFF. When bound to activator proteins,
they prevent the activator’s binding to the activator binding site. When bound to repressor proteins,
they facilitate the repressor’s binding to the operator.

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10
Q

The lac operon controls

A

lactose catabolism through the expression of lacZYA genes

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11
Q

What is the lac operon a classic example of?

A

negative regulation of transcription initiation

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12
Q

components of the lac operon

A

▪ LacI: repressor protein
▪ Allolactose: inducer of LacI
▪ CRP: activator protein
▪ cAMP: inducer of CRP

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13
Q

what is a better energy source, glucose or lactose?

A

glucose

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14
Q

catabolite repression

A

since glucose is a better energy source than lactose, when glucose is present, the operon needs to be repressed so energy is not wasted producing genes to get energy from lactose

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15
Q

When glucose is present…

A

The activity of adenylate cyclase (the enzyme that produces cAMP) is inhibited; thus, CRP induction does not occur.

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16
Q

When glucose is absent,

A

Adenylate cyclase is activated, leading to the production of cAMP, allowing CRP to bind and recruit RNAP.

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17
Q

When lactose is present,

A

It is readily converted to
allolactose, which induces the LacI repressor, allowing
RNAP to proceed with transcription

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18
Q

When lactose is absent,

A

LacI is not induced and
Therefore remains bound to the operator, preventing
RNAP.

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19
Q

major operator

A

O1

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20
Q

Monomeric LacI

A

Monomeric LacI can bind O1 and sterically inhibit RNAP

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21
Q

tetrameric LacI

A

can bind O1 in conjunction with either O2 or O3, forming a secondary structure that makes the promoter inaccessible to RNAP.

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22
Q

ara operon

A

controls arabinose catabolism through the expression of araBAD genes

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23
Q

The ara operon is a classic example of

A

positive regulation of transcription initiation.

24
Q

Components of the ara operon include:

A

AraC: regulator protein that can act
as either an activator or a repressor
▪ CRP: activator protein
▪ cAMP: inducer of CRP
▪ Arabinose: inducer of AraC

25
The operon contains
two operators (O1 and O2), and an activator region containing a CRP-binding site and two other regulatory sites (I1 and I2).
26
Attenuation
is a form of transcriptional control in Bacteria and Archaea that functions by prematurely terminating mRNA synthesis
27
Attenuation is most common in
in controlling amino acid biosynthesis.
28
In attenuation, the first part of the mRNA to be made
called the leader sequence,
29
leader sequence
can fold into two alternative secondary structures.
30
One mRNA secondary structure allows
continued synthesis of the mRNA, whereas the other secondary structure causes premature termination.
31
Secondary structure formation depends either on
events at the ribosome or on the activity of regulatory proteins.
32
Stem loops can form between...
2:3 and 3:4.
33
which is the more energetically favorable stem loop?
The 2:3 stem loop is more energetically favorable so if all regions 2-4 are accessible than the 2:3 loop will form
34
2:3 stem loop
anti-attenuator loop that allows RNAP to transcribe the trp operon.
35
3:4 stem loop
an attenuator loop that prevents RNAP from transcribing the trp operon.
36
The leader sequence (region 1) of the trp operon encodes
a peptide rich in tryptophan amino acids.
37
When tryptophan levels are high,
the ribosome can translate through the leader sequence to region 2. With the ribosome blocking region 2, the attenuator loop (i.e., the 3:4 stem loop) can form and RNAP is disengaged, preventing biosynthesis of more tryptophan.
38
With the ribosome blocking region 2,
the attenuator loop (i.e., the 3:4 stem loop) can form and RNAP is disengaged, preventing biosynthesis of more tryptophan.
39
When tryptophan levels are low,
the ribosome cannot translate through the leader sequence, leaving region 2 available for binding to form the anti- attenuator loop (i.e., the 2:3 stem loop), allowing transcription to proceed to enable tryptophan biosynthetic genes to be expressed.
40
What signals the formation of the transcriptional terminator in the trp operon during attenuation? a. Binding of tryptophan to the repressor b. Interaction between the ribosome and mRNA c. Binding of RNA polymerase to the promoter
b. Interaction between the ribosome and mRNA
41
What are riboswitches?
Riboswitches are RNA molecules (often in the 5′-UTR) that bind small metabolites and regulate gene expression, similar to repressors or activators
42
Where are riboswitches usually located in relation to coding sequences?
Upstream of coding regions in the 5′-UTR
43
What is the name of the riboswitch region that binds the ligand?
The aptamer region — it folds into specific 3D structures to recognize the ligand.
44
How many structural forms can a riboswitch aptamer adopt?
Two — one ligand-bound and one unbound, each leading to different downstream effects.
45
What determines whether the riboswitch folds into its ligand-bound or unbound structure?
The presence or absence of the ligand (small molecule).
46
What is the expression platform in a riboswitch?
The downstream RNA region whose secondary structure is controlled by the aptamer and determines whether transcription continues or stops.
47
How does ligand binding to the aptamer affect transcription?
It influences the formation of either a terminator loop or an anti-terminator loop in the expression platform.
48
What happens if a terminator loop forms?
Transcription is terminated before the expression platform is transcribed.
49
What happens if an anti-terminator loop forms?
Transcription proceeds, allowing expression of the downstream genes.
50
What is the overall role of riboswitches in bacteria?
They act as direct sensors of metabolites, controlling transcription (and sometimes translation) without proteins.
51
How do riboswitches regulate gene expression at the translational level?
By controlling the accessibility of the ribosome binding site (RBS) through structural changes in the RNA.
52
What happens if ligand binding causes the RBS to become occluded?
The expression platform is unavailable, and translation is blocked.
53
What happens if ligand binding causes the RBS to become exposed?
The expression platform is open, allowing the ribosome to bind, and translation proceeds.
54
What region of the riboswitch binds the ligand to trigger these structural changes?
The aptamer region.
55
What determines whether the RBS is exposed or occluded?
The presence or absence of the ligand influences the RNA secondary structure.