Bacterial Gene Expression 2 Flashcards

1
Q

trp operon - Genes and Order

A

-the trp operon consists of 5 genes encoding enzymes of the shikimate pathway that converts chorismate to tryptophan (an amino acid)
-the trp operon is only expressed when tryptophan is required in the cell
promoter-operator-trpL—-trpE-trpD-trpC-trpB-trpA

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2
Q

Regulation of trp operon at Transcription Initiation Level

A
  • repressible operons
  • a small molecule, tryptophan, facilitates the binding to DNA of a transcription factor
  • the repressor of the trp operon, TrpR, binds to the operon only when it is bound by the co-repressor, tryptophan
  • this is the opposite of the control of the lac operon
  • tryptophan acts as a co-repressor with TrpR, not an inducer
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3
Q

How do we know that there is a second level of regulation of the trp operon?

A
  • TrpR reduces transcription of the trp operon by 70x
  • but the presence of tryptophan leads to a decrease in the level of the trp operon enzymes by 560-700x
  • this means that there must be another level of regulation
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4
Q

Second Level of Regulation of the trp Operon

Outline

A
  • the second regulatory mechanism is also at the level of transcription but occurs after initiation
  • it is called attenuation and causes transcription termination before RNA polymerase can reach the first gene of the operon, trpE
  • cis-acting regulatory elements are in the 5’ leader of the mRNA called TrpL, between the 5’ end and the start codon of TrpE
  • within trpL is a sequence called the attenuator
  • the attenuator contains a short open reading frame that contains 4 segments that can form three alternative secondary structures depending on the levels of tryptophan in the cell
  • segment one contains a run of many consecutive tryptophan codons
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5
Q

Second Level of Regulation of the trp Operon

Low Tryptophan

A
  • if tryptophan levels in the cell decrease
  • then levels of tRNAs with tryptophan also decrease
  • a ribosome following behind the RNA polymerase will stall when it reaches segment 1 as there aren’t enough tRNAs
  • the ribosome is covering region 1
  • RNA polymerase continues ahead and transcribes segements 2 and 3
  • segment 1 is covered so segment 2 cant bind to it, instead segments 2 and 3 bind
  • region 4 is left unpaired and RNA polymerase can continue to transcript the trp operon genes
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6
Q

Second Level of Regulation of the trp Operon

High Tryptophan

A
  • ribosome doesn’t stall at region 1 as there are enough tryptophan tRNAs
  • the ribosome proceeds to the stop codon between segments 1 and 2 and stops partially covering segment 2
  • when RNA polymerase synthesises region 3 it cant pair with region 2, instead it pairs with region 4
  • the pairing of segments 3 and 4 creates a rho-independent transcriptional terminator
  • RNA polymerase doesn’t reach the genes of the trp operon
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7
Q

pheA

A

-like the trp operon, uses a repressor to switch ON/OFF expression of the operon and uses attenuation to fine tune expression

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8
Q

CREs

A
  • cis-regulatory elements
  • regions of non-coding nucleic acid that regulate expression of co-localised genes
  • found in the vicinity of the genes they regulate
  • typically regulate gene expression by functioning as binding sites for other factors, including but not limited to proteins
  • cis - on this side
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9
Q

Trans-acting Factors

A
  • encode diffusible factors that can regulate the expression of genes at a distance
  • trans - on a different side
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10
Q

Eubacterial Translation Initiation

A
  • ribosomes start at the start codon (usually AUG, but sometimes GUG or UUG) within 5-8 bp of the RBS (ribosome binding site on the mRNA
  • the RBS has a degree of complimentarity to a segment of 16S rRNA in the ribosome
  • similarity to consensus can determine the efficieny of translation
  • translation initiation is a major point of gene regulation in eubacteria
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11
Q

Regulation at Level of Translation Initiation

A
  • ribosomal subunit assembly is highly coordinated
  • synthesis of ribosomal proteins never exceeds that which can be assembled with RNA to produce complete translational machinery
  • underlying mechanism of auto-regulation of translation
  • if
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12
Q

Regulation of Translation Without Protein Binding - prfA

A
  • in human pathogen Listeria which causes food poisoning
  • virulence genes are only expressed at 37C (human body temperature)
  • transcription factor regulating these virulence genes is prfA
  • expression of prfA is controlled at the level of transcription
  • mRNA of prfA has a 5’ leader sequence that can form a secondary structure
  • this secondary structure incorporates the Shine-Dalgarno sequence (RBS)
  • ribosomes can only access the S-D sequence when the secondary structure melts which occurs at 37C
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13
Q

Regulation of Translation by Small RNAs - ompF

A
  • ompF gene encodes a major outer membrane porin
  • a porin is a non-specific transport that allows the passive diffusion of small, polar molecules
  • translation of pre-made ompF mRNA is regulated
  • antisense RNA from micF gene is synthesised which is complimentary to ompF mRNA
  • the antisense RNA from micF binds to the ompF RNA to prevent translation initiation
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14
Q

RNA Regulation Beyond Anti-Sense RNAs

A
  • 6S RNA mimics a promoter recognised by sigma 70
  • it binds to and inhibits RNA polymerase
  • a regulation of transcription initiation
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15
Q

Why use sRNAs instead of proteins to regulate gene expression?

A
  • RNA world hypothesis - a world filled with RNA-based life which predates current DNA-based life
  • RNA can store information like DNA and catalyse reactions like proteins do, may have supported pre-cellular life
  • RNA worl evolved into a DNA world
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16
Q

CRISPR

A
  • clustered regularly interspaced short palindromic sequences
  • an antisense RNA guide system found in prokaryotes
  • part of the bacterial immune system
  • prevents expression of foreign genes
  • found in the genomes of many bacteria, ~40% eubacteria and ~85% of archaea
17
Q

CRISPR - CAS

A
  • CRISPR sequences are associate with groups of genes called CAS genes
  • CRISPR repeat sequences (24-48bp) are separated by unique sequences / spacers of similar length
  • spacer sequences are usually unique within the genome
  • CRISPR/Cas is an adaptive defence system against invasive nucleic acids
  • the repeat-spacer region is transcribed into a long polyspacer RNA which is cleaved into smaller antisense RNAs to form CRISPR RNAs, crRNAs
  • these crRNAs bind to the genome at target sites and make double stranded breaks
  • RNAs serve as guides for an effector complex that is composed of certain cas proteins, Cas 9
  • the effector complex is what cleaves the DNA to make the double stranded break
18
Q

Where do spacers come from?

A
  • spacers are derived from mobile genetic elements (MGEs) i.e. plasmids and vectors
  • sequences within MGEs are called proto-spacers