Lecture 3 Flashcards

1
Q

what are the 2 types of negative and positive regulation?

A

negative regulation - turn gene on via removing a repressor
- addition of ligand to turn gene on (removing repressor)
- removal of ligand to turn gene on (removing repressor)

positive regulation - turning gene off via removal of activator
- addition of ligand to turn gene off (removing activator)
- removal of ligand to turn gene off (removing activator)

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2
Q

what is negative regulation for prokaryotic gene regulation

A

Competition between RNA
polymerase and repressor protein for promoter binding

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3
Q

what is positive regulation for prokaryotic gene regulation

A

Activator protein recruits RNA
polymerase to the promoter to activate transcription

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4
Q

where are gene regulatory elements found

A
  • regulatory elements are found close to the transcriptional start site of prokaryotic genes

BUT regulatory elements can also be found:
* Far upstream of gene
* Downstream of gene (eukaryotes)
* Within gene (introns; eukaryotes)

  • these elements are found far from the transcriptional start site but can still influence transcription
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5
Q

how does the NtrC protein - transcriptional activator activate transcription

A
  • NtrC protein is a transcriptional activator found downstream of the gene
  • DNA looping allows NtrC to directly interact with RNA polymerase to activate transcription even from a distance
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6
Q

what is bacteriophage lambda

A

it is a virus that infects bacterial cells
- the lambda virus attaches to the host cell and injects the lambda dna
- lambda dna circularizes
- can exists in one of two stages of bacteria

  • the Positive and negative regulatory mechanisms work together to regulate
    the lifestyles of bacteriophage lambda
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7
Q

bacteriophage lambda can exists as one of two states in bacteria: explain the two
- under favourable bacterial growth conditions
- under damaged host cell conditions

A
  1. under favourable bacterial growth conditions
    - integration of lambda dna into the host chromosome
    - the dna joins the host chromosome continuously
    - integrated lambda dna replicates along the host chromosome
    - prophage pathway
  2. when the host cell is damaged
    - from bacterial outcome one (prophase pathway) an induction event may occur (host response to dna damage)
    - synthesis of viral proteins needed for the formation of new viruses
    - rapid replication of lambda dna and its packaging into complete viruses
    - cell lysis releases a large number of new viruses
    -lytic pathway

Two gene regulatory proteins are responsible for initiating this switch and actually repress each other’s synthesis…the lambda repressor protein (cl) and lambda cro protein

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8
Q

what are the two gene regulatory proteins that are responsible for initiating the switch between prophage and lytic pathways

A
  • Lambda repressor protein from prophage state (cI) and lambda Cro protein from lytic state

They repress each other’s synthesis, giving rise to the two stable states

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9
Q

explain the molecular biology that occurs in prophage state 1 with its gene regelatory protein

slide 11 DIAGRAM

A
  • lambda repressor is made by a cl gene

Lambda repressor occupies the operator next to the same gene its made from:
* blocks synthesis of Cro
* activates its own synthesis (loop)
* most bacteriophage DNA not transcribed

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10
Q

explain the molecular biology that occurs in lytic state 1 with its gene regulatory protein

slide 12 DIAGRAM

A
  • lambda Cro protein is made by a Cro gene

Cro occupies the operator next to the same gene its made from:
* blocks synthesis of lambda repressor
* allows its own synthesis (loop)
* most bacteriophage DNA is
extensively transcribed
DNA is replicated, packaged, new bacteriophage released by host cell lysis

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11
Q

What triggers the switch between prophage and lytic states in bacteriophage lambda?

what is the prophage-lytic control an example of?

A

It’s host response to DNA damage!
An induction event occurs only when the host/DNA is damaged.
➢ DNA damaged? switch to lytic state inactivates lambda repressor

Under good growth conditions (ie. DNA is not damaged), lambda repressor protein blocks Cro and activates itself in a positive feedback loop
➢ maintains prophage state

the prophage-lytic circuit is an example of a transcriptional circuit – other types of circuits controls various biological processes

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12
Q

what are 4 types of transcriptional circuits? list examples, and how it is conducted

A
  1. positive feedback loop - ex. lambda repressor protein - production of protein A from gene A. positive loop so it effects transcription of itself (making A protein)
  2. negative feedback loop - production of protein A from gene A. negative loop so it effects transcription of itself (repressing A protein)
  3. flip-flop device (indirect positive feedback loop) ex. Cro repressor switch - a protein is made from gene a, and inhibits DNA B. B gene is made and inhibits DNA A. But these CANNOT work at the same time since repression is occuring.
  4. feed forward loop - (ex. the repressilator) A protein is made, promotes DNA B and DNA Z. B protein is made and ALSO promotes DNA Z. Z protein is made (requires signals from both A and B)
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13
Q
  1. Positive feedback loops

how are positive feedback loops used to create cell memory

A
  • there is a parent cell which has gene A but never creates protein A because it is required for the transcription of its own gene
  • then there is an initial transient signal which turns on the expression of gene A
  • this results in the A to produce more and more A as the positive feedback loop acts on itself
  • now when this cell divides, every daughter cell will be turned on to produce more and mor A via the positive feedback loop
  • this is always because of that one initial signal that was sent – cell memory is created forever because of one transient signal
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14
Q

what are feed forward loops? how do they measure the duration of a signal?

A
  • a feed forward loop is based on sensitivity
  • A protein is made, promotes DNA B and DNA Z. B protein is made and ALSO promotes DNA Z. Z protein is made (requires signals from both A and B)
  • you need a prolonged input of B or A to stimulate the production of protein Z. if there is only a brief stimulus it will not cause protein Z to be produced.
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15
Q

what is synthetic biology?

A
  • Combinations of regulatory
    circuits combine in eukaryotic
    cells to create exceedingly
    complex regulatory networks
  • Scientists can construct
    artificial circuits and examine
    their behavior in cells. This is
    called synthetic biology
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16
Q

what is the repressilator example from synthetic biology?
- what are the three proteins produced in the repressilator
- what did the authors predict what would happen if the flip-flop transcriptional circuit took place?
- where did they introduce this circuit to in order to test it?

A

scientists wanted to construct an artifical circuit for the sake of creating something (aka synthetic biology) and thus created a simple gene oscillator using a delayed negative feedback circuit

the three proteins produced:
A: Lac repressor
B: Tet repressor (response to antibiotic)
C: Lambda repressor

Predicted: delayed negative feedback gives rise to oscillations

Introduced this circuit into bacterial cells and
observed expression of the repressor genes

17
Q

how does the repressilator work ?

slide 21 DIAGRAM

A
  1. A repressor protein is expressed
  2. A repressor protein binds to the A binding site on gene B, thus repressing the synthesis of B repressor protein
  3. Since nothing is bound to the repressor B binding cite on gene c, c repressor protein is produced
  4. c repressor protein loops back to gene A and represses A protein expression (note the A protein produced in step 1 is degraded by this time)
  5. since A protein repressor is not produced, nothing binds to repressor binding site A on gene B, thus protein repressor B is expressed
  6. B repressor protein binds to gene C, and represses C repressor protein synthesis
  7. repeat 1-4

its a loop!

18
Q

did the repressilator gene circuit work as the researchers predicted?

A
  • no
  • the researchers predicted that the genes would oscillate perfectly
  • in actuality, the genes somewhat oscillated but also increased with amplitude at time went on
  • this was due to increasing bacterial growth in the system through time – delayed feedback loop
19
Q

what is transcriptional attenuation

A
  • In both prokaryotes and eukaryotes there can be a premature termination of transcription called transcription attenuation
  • RNA adopts a structure that interferes with RNA polymerase so transcription may be stopped earlier
  • Regulatory proteins can bind to RNA and interfere with attenuation
  • Prokaryotes, plants and some fungi also use riboswitches to regulate
    gene expression
20
Q

what are riboswitches and the different types?

A
  • Short RNA sequences that change conformation when bound by a small molecule
  • different types: some riboswitches conduct transcription attenuation and some dont.

eg. prokaryotic riboswitch that regulates purine biosynthesis is a riboswitch which does regulate genes via transcription attenuation

21
Q

what are pyrimidines and purines - review of hs bio
- what bases
- how many rings

A

pyrimidines
- U, C, T
“you see the pyramids”
- 1 ring

purines
- A, G
- 2 rings

22
Q

explain how the prokaryotic riboswitch works to regulate purine biosynthesis

A

Low guanine levels
- Transcription of purine biosynthetic genes is on

High guanine levels
* Guanine binds riboswitch
* Riboswitch undergoes
conformational change which changes a portion of the RNA into a transcription terminator
* Causes RNA polymerase to
terminate transcription before it even gets to the AUG start codon (premature transcription termination)
* Transcription of purine
biosynthetic genes is off