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MB 206 : Module 1 - B

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Regulation of Gene Expression in Bacteria Angelia Teo Jan 09 – PowerPoint PPT presentation

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Title: MB 206 : Module 1 - B


1
MB 206 Module 1 - B
  • Regulation of Gene Expression in Bacteria

2
This diagram is for eukaryote
3
Regulation of Gene Expression
  • A cell contains the entire genome of an organism
    ALL the DNA.
  • Gene expression transcribing and translating
    the gene
  • Regulation allows an organism to selectively
    transcribe (and then translate) only the genes it
    needs to.
  • Genes expressed depend on
  • the type of cell
  • the particular needs of the cell at that time.

4
Principles of Gene Regulation
In genetics, constitutive refers to a gene
product made all the time. In the absence of
the activator or the repressor, RNA polymerase
transcribes the gene constitutively
A gene is expressed in higher level under
influence of some signal
5
How Are Genes Regulated?
  • Genes located in coherent packages called operons
  • operons has 4 parts
  • regulatory gene - controls timing or rate of
    transcription
  • promoter - starting point
  • operator - controls access to the promoter by RNA
    polymerase
  • structural genes
  • NOTE operons regulated as units

6
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7
Gene Regulation in Prokaryotes
  • Prokaryotes organize their genome into operons
  • Operon a group of related genes
  • One promoter sequence at the very beginning
  • All of the genes will be transcribed together (in
    one long strand of RNA.

8
Principle of Gene Regulation
  • RNA polymerase binds to DNA at promoters.
  • Transcription initiation is regulated by proteins
    that bind to or near promoters.
  • Repression of a repressible gene (i.e., negative
    regulation) repressors (vs activitors) bind to
    operators of DNA.
  • Repressor is regulated by an effector, usually a
    small molecules or a protein, that binds and
    causes a conformational change.
  • Activitor binds to DNA sites called
  • enhancer to enhance the RNA
  • polymerase activity.
  • (i.e., positive regulation)
  • Induction of an inducible gene, e.g., heat-shock
    genes.

9
General organization of an inducible gene
10
Regulation of Genes

Transcription Factor (Protein)
RNA polymerase
DNA
Regulatory Element
Gene
11
Regulation of Genes

New protein
RNA polymerase
Transcription Factor
DNA
Gene
Regulatory Element
12
Gene Expression
How much protein is in a cell (and active)??
13
Most genes are not expressed at a particular time
  • Not all of the genes in a bacteria will be
    expressed at the same time.
  • Even in some of the smallest bacteria, about 500
    different genes exists
  • Of the 4279 genes in E. coli , only about 2600
    (60) are expressed in standard laboratory
    conditions.
  • Only about 350 genes are expressed at more than
    100 copies (i.e. molecules!) per cell, making up
    90 of the total protein.

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16
Possible target in control of gene expression
17
Topics
  • Lac Operon (Negative control Catabolic
    repression)
  • Tryptophan Operon (Positive control)
  • Histidine Operon (Attenuator)

18
Comparison of genomes of various organism

ORGANISM coding Size of genome (bp) number of genes
Escherichia coli 90 4,639,221 bp 4288
Mycoplasma genitalium 88 580,073 bp 468
Haemophilus influenzae 86 2,087,778 bp 1,662
Methanococcus jannaschii 85 1,660,000 bp 1,997
Synechocystis sp. (PCC 6803) 80 3,570,000 bp 3,168
Saccharomyces cerevisiae 75 13,000,000 bp 6,275
Humans 2 3,000,000,000 bp 70,000 (?)
19
Diploid numbers of some commonly studied organisms(as well as a few extreme examples) Diploid numbers of some commonly studied organisms(as well as a few extreme examples)
Homo sapiens (human) 46
Mus musculus (house mouse) 40
Drosophila melanogaster (fruit fly) 8
Caenorhabditis elegans (microscopic roundworm) 12
Saccharomyces cerevisiae (budding yeast) 32
Arabidopsis thaliana (plant in the mustard family) 10
Xenopus laevis (South African clawed frog) 36
Canis familiaris (domestic dog) 78
Gallus gallus (chicken) 78
Zea mays (corn or maize) 20
Muntiacus reevesi (the Chinese muntjac, a deer) 23
Muntiacus muntjac (its Indian cousin) 6
Myrmecia pilosula (an ant) 2
Parascaris equorum var. univalens (parasitic roundworm) 2
Cambarus clarkii (a crayfish) 200
Equisetum arvense (field horsetail, a plant) 216
20
Genes in E.coli
21
E.coli genes expressed
  • A total of 4288 genes in Escherichia coli
  • - 2600 genes found under standard
    laboratory growth conditions
  • - 2100 protein spots detected under 2-D
    protein gels
  • - 350 proteins in high amount, the rest
    are very low amounts
  • Majority of the genes are likely to be expressed
    transiently, in small amounts during DNA
    replication, and then remain silent (unexpressed)
    until the next round of DNA synthesis

22
Why is there a need to control gene expression?
  • 1) Prevent energy wastage
  • 2) Ensure only necessary proteins are made
    according to the requirement for cells growth.
  • Small portion of DNA in cell used for genetic
    message (mRNA), the rest for regulatory purposes.

23
Gene Regulation in bacteria
  • How do single-celled prokaryotes like E. coli
    know how to respond to their environments?
  • Each environmental cue generates a specific
    response, with specific proteins and reactions.
  • eg.
  • A bacterium can use different sources of
    Nitrogen
  • - incorporate N2 gas from the air
  • - incorporate ammonia from their
    surroundings or
  • - from amine group of an amino acid like
    glutamine (easier and less energy)
  • These processes involve very different
    enzymes. Presence of glutamine, the cell will
    turn off synthesis of enzymes for fixing N2

24
How can the cell "turn off" the synthesis of
proteins from its DNA?

25
Gene regulation can occur at any place along the
flow of information from DNA to RNA to protein
26
Different forms of gene regulation
  • a. Regulation by DNA Replication (default)
  • b. Transcriptional Regulation by different
    s-factors.
  • c. Negative Regulation of Gene Expression
  • d. Positive Control of Gene Regulation
  • e. Alternative splicing of RNA (almost
    exclusively for eukaryotes)
  • f. Post-transcriptional regulation
  • - termination of transcription
  • - translation control - message
    stability - protein stability

27
E.coli RNA Polymerase subunits

Gene Mass KDa Use -35 Sequence separation -10 Sequence
rpoA 40 a subunit - - -
rpoB 155 b subnit - - -
rpoC 160 b' subunit - - -
rpoD 70 s70 General TTGACA 16-18 bp TATAAT
rpoN 54 s54 Nitrogen CTGGNA 6 bp TTGCA
rpoS 38 s38 Stationary not known not known not known
rpoH 32 s32 Heat shock CCCTTGAA 13-15 bp CCCGATNT
fliA 28 s28 Flagellar CTAAA 15 bp GCCGATAA
rpoE 24 s24 High temp. heat shock not known not known not known
28
Transcription regulation by s-factors
  • s70 - RpoD normal s-factor s54 - RpoN
    Nitrogen response s38 - RpoS Stationary
    phase s32 - RpoH Heat shock response s28
    - FliA Flagellar genes regulation s24 -
    RpoE Heat shock high temp.
  • Approx 1500 - 2000 copies of RNAP holoenzyme/
    cell
  • For bacteria growing in "log phase"
  • 600 copies of RpoD (s70)
  • 200 copies of RpoS (s38)
  • RpoS increases to 600 copies per cell in
    stationary phase or osmotic shock.

29
Operon and Regulon
  • An operon
  • - consists of a set of genes expressed
    coordinately transcribed
  • as a single unit
  • - Specific regulation (positive / negative)
    can induce or repress a
  • particular gene or operon
  • - contains both a regulatory a message
    region.
  • - Regulatory / control region at the 5
    side of the gene codes for a
  • protein (message region).
  • Regulon
  • - comprise of global regulation affecting a
    set of operons.
  • - All operons in the regulon are
    coordinately controlled by the
  • same regulatory mechanism.

30
Operons-the basic concept of Prokaryotic Gene
Regulation
  • Regulated genes can be switched on and off
    depending on the cells metabolic needs
  • Operon a regulated cluster of adjacent
    structural genes, operator site, promotor site,
    and regulatory gene(s)

31
Repressible vs. Inducible Operonstwo types of
negative gene regulation
  • Repressible Operons
  • Genes are initially ON
  • Anabolic pathways
  • End product switches off its own production
  • Inducible Operons
  • Genes are initially OFF
  • Catabolic pathways
  • Switched on by nutrient that the pathway uses

32
lac an inducible operon
33
The lac Operon of E. coli
  • 1. Growth and division genes of bacteria are
    regulated genes. Their expression is controlled
    by the needs of the cell as it responds to its
    environment with the goal of increasing in mass
    and dividing.
  • 2. Genes that generally are continuously
    expressed are constitutive genes (housekeeping
    genes). Examples include protein synthesis and
    glucose metabolism.
  • 3. All genes are regulated at some level, so that
    as resources dwindle the cell can respond with a
    different molecular strategy.
  • 4. Prokaryotic genes are often organized into
    operons that are cotranscribed. A regulatory
    protein binds an operator sequence in the DNA
    adjacent to the gene array, and controls
    production of the polycis-tronic (polygenic)
    mRNA.
  • 5. Gene regulation in bacteria and phage is
    similar in many ways to the emerging information
    about gene regulation in eukaryotes, including
    humans. Much remains to be discovered even in E.
    coli, one of the most closely studied organisms
    on earth, 35 of the genomic ORFs have no
    attributed function.

34
The lac Operon of E. coli
  • Animation Regulation of Expression of the lac
    Operon Genes
  • 1. An inducible operon responds to an inducer
    substance (e.g., lactose). An inducer is a small
    molecule that joins with a regulatory protein to
    control transcription of the operon.
  • 2. The regulatory event typically occurs at a
    specific DNA sequence (controlling site) near the
    protein-coding sequence (Figure 16.1).
  • 3. Control of lactose metabolism in E. coli is an
    example of an inducible operon.

35
Lac Operon
  • Transcription is OFF
  • When there is no lactose that needs to be
    digested
  • lacI repressor is in active form ? binds to
    operator ? blocks RNA Polymerase ? no
    transcription

36
Lac Operon
  • Transcription is ON
  • When there is lactose that needs to be digested
  • Lactose binds to lacI repressor ? inactivates it
  • RNA Polymerase is able to bind to promoter ?
    transcribe genes

37
Negative Regulation of Gene Expression
  • By default, the gene is usually
  • switched ON.
  • Binding of a REPRESSOR will switch
  • the gene OFF.
  • Most common regulation in BACTERIA
  • Often this is found as AUTOREGULATION - where too
    much of the gene product inhibits further
    transcription - usually this is through binding
    to the upstream promoter control region.
  • A good "classic" example is the E.coli lac
    operon.

38
Positive control of Regulation
  • By default, the gene is usually
  • switched OFF.
  • Binding of a ACTIVATOR will switch
  • the gene ON. (often transcriptional
    activators / factors
  • bind and bend DNA upstream of the
    promoter.)
  • Most common in EUKARYOTES
  • Some promoters are not very functional in the
    absence of a transcriptional activator
    protein(s).

39
Lac Operon
  • Lactose metabolism occurs when the environment
    contains lactose.
  • Enzymes required for lactose degradation are
    TURNED ON.
  • beta-galactosidase (lac Z)
  • - enzyme hydrolyzes the bond between glucose
    galactose.
  • Lactose Permease (Lac Y)
  • - enzyme spans the cell membrane
  • - transports lactose into the cell from
    the outside environment.
  • - Membrane is otherwise essentially
    impermeable to lactose.
  • Thiogalactoside transacetylase (LacA)
  • - The function of this enzyme is not known.

40

Lactose metabolism
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42
Regulatory elements in the Lac Operon
Element
Function Operator (LacO) binding site for
repressor Promoter (LacP) binding site
for RNA polymerase Repressor (LacI)
codes for lac repressor protein
Binds to DNA at
operator and blocks binding of
RNA polymerase at promoter Pi promoter
for Lac I CAP
binding site for cAMP/CAP complex
43
  • Glucose or Lactose?
  • A bacterium's prime source of food is glucose,
    since it does not
  • have to be modified to enter the respiratory
    pathway.
  • So if both glucose lactose are around, the
    bacterium will
  • to turn off lactose metabolism in favor of
    glucose metabolism.
  • There are sites upstream of the Lac genes that
    respond
  • to different glucose concentrations.

44
Presence of inducer - lactose
45
Regulation of Lac operon - depending on
availability of lactose or glucose
Low levels of Glucose / Catabolite repression
Absence of lactose
46
  • Regulation of Lac Operon
  • When lactose is present, it acts as an inducer of
    the operon. Lactose enters the cell and binds to
    the Lac repressor, inducing a conformational
    change preventing the repressor from binding to
    the operator. This allows the RNA polymerase
    binding at the promoter to proceed with
    transcription of mRNA (LacZ, LacY LacA) and
    production of enzymes for the metabolism of
    lactose.
  • When the inducer (lactose) is removed, the
    repressor returns to its original conformation
    and binds to operator, blocking the RNA
    polymerase from proceeding with transcription of
    mRNA, thus no protein is made.
  • The lac operon is always primed for transcription
    upon the addition of lactose.
  • When levels of glucose (a catabolite) in the cell
    are high, formation of cyclic AMP is inhibited.
    But when glucose levels drop, more cAMP forms.
    cAMP binds to a protein called CAP (catabolite
    activator protein), which is then activated to
    bind to the CAP binding site. This activates
    transcription, by increasing the binding affinity
    of RNA polymerase to promoter. This is called
    catabolite repression, a misnomer since it
    involves activation, but understandable since it
    seemed that the presence of glucose repressed all
    the other sugar metabolism operons.

47
The Tryptophan Operon (Positive regulation)
  • Trp operon contains the Tryptophan biosynthetic
    genes.
  • Trp repressor protein can bind to the operator of
    Trp operon
  • When tryptophan is high, it binds to the
    repressor and induces a change so that the
    repressor can now bind to DNA.
  • When tryptophan are low in the cell, tryptophan
    falls off the repressor, and the repressor goes
    back to its original conformation, losing its
    ability to bind to the DNA. RNA polymerase binds
    to the promoter and transcription proceeds,
    making tryptophan biosynthetic genes and
    replenishing the cell's supply of tryptophan.
  • This type of feedback inhibition of transcription
    is very common. ribosomal RNA can also act to
    repress their own synthesis.

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Repressible Operon Trp Operon
  • Repressible Operon Operon that is usually ON
    but can be inhibited
  • The Trp Operon
  • example of a repressible operon
  • Genes that code for enzymes needed to make the
    amino acid tryptophan

50
TrpR Gene
  • TrpR gene is the regulatory gene for the Trp
    operon
  • Found somewhere else on the genome
  • NOT part of the Trp operon
  • TrpR gene codes for a protein TrpR repressor
  • TrpR gene is transcribed and translated
    separately from the Trp operon genes.

51
TrpR Repressor
  • Repressor protein is translated in an inactive
    form
  • Tryptophan is called a corepressor
  • When tryptophan binds to the TrpR repressor, it
    changes it into the active form

52
Operator Region
  • There is also an operator region of DNA in the
    Trp Operon
  • Just after the promoter region
  • The TrpR Repressor can bind to the operator if
    its in the active form

53
Trp Operon
  • Transcription is ON
  • Occurs when there is no tryptophan available to
    the cell.
  • Repressor is in inactive form (due to the absence
    of tryptophan)
  • RNA Polymerase is able to bind to promoter and
    transcribe the genes.

54
Trp Operon
  • Transcription is OFF
  • Occurs when tryptophan is available
  • Tryptophan binds to the TrpR repressor ? converts
    it to active form
  • TrpR protein binds to operator ? blocks RNA
    Polymerase ? no transcription

55
trp a repressible operon
56
Question
  • Under what conditions would you expect the trp
    operon to go from OFF to ON again?
  • When there is no longer tryptophan available all
    of it has been used up

57
The Histidine Operon (An Attenuator)
  • The histidine operon functions in a slightly
    different way.
  • At the beginning of the operon there is a leader
    coding region
  • AUG-AAA-CGC-GUU-CAA-UUU-AAA-CAC-CAC-CAU-CAU-CAC-
    CAU-CAU-CCU-GAC
  • Met-Thr-Arg-Val-Gln-Phe-Lys-His-His-His-His-His-
    His-His-Pro-Asp
  • When transcription begins, the RNA comes of
    the DNA and ribosomes hop onto it to start
    translation.
  • Low amount of histidine in the cell
  • - the ribosome stalls because no aminoacyl
    tRNA's charged with histidine.
  • - this leaves a long stretch of RNA (for
    RNA ploymerase is still transcribing
  • it) with no ribosomes bound to it.

58
The Histidine Operon (An Attenuator)
  • High amount of histidine in the cell
  • - the ribosome is not stalled
  • - the leader sequence in RNA allows it to
    form a terminator loop
  • (attenuation site), at which point the
    RNA is cleaved
  • - RNA polymerase stops transcribing the
    genes
  • - the terminator only functions when the
    ribosome is not stalled.
  • Many amino acid synthetic operons are also
    controlled by some form of attenuation. The
    tryptophan operon has both attenuation control
    and repressor control.

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Methods for Studying Regulation
  • Possible mutations in various elements of the Lac
    operon, give rise to mutants
  • How to study the lac operon? Tools used
  • IPTG (isopropyl-beta-D-thiogalactoside)
  • - a molecule analogue to lactose, binds to
    the Lac repressor (Lac I).
  • - used as a gratuitous inducer to induce
    Lac operon
  • - but not a substrate for the lactose
    metabolism genes.
  • Spectrophotometer quantification of
    B-galactosidase activity.
  • - Quantify amount of mRNA made (coding
    lacZ, lacY, and lacA)
  • - B-galactosidase can cleave a colourless
    substrate called ONPG into a
  • yellow product , ONP - quantitated by
    spectrophotometer.
  • - The degree of yellowness - indicates
    enzyme activity or amount of
  • transcription of mRNA or the activity of
    lac operon.

61
Methods for Studying Regulation
  • Different types of gene expression
  • - Constitutively ( c ) expressed gene is
    never turned off, it is
  • making mRNA and protein all the time.
  • - Inducible gene can be turned on by an
    inducer.
  • - Uninducible gene is never turned on. DNA
    binding site is
  • mutated preventing binding by an
    inducer.
  • - Super-repressor ( s ) always represses,
    regardless
  • of its regulation. eg. a Lac I (s)
    mutant always represses the
  • promoter whether or not lactose is
    present.

62
Cis or Trans-regulation
  • DNA element 1 and DNA element 2
  • How to determine whether DNA element 1 is
    acting in cis or in trans to one another ?
  • Test insert a piece of DNA carrying DNA
    element 1 into a cell that already has a copy of
    mutated DNA element 1 adjacent to DNA element 2.
  • A) Observation the cell recovers its
    function.
  • Conclusion The inserted element can
    complement or replace the function of the mutated
    element 1, it can be said to be trans acting,
    since it must diffuse off a plasmid or from
    another site in the DNA in order to be
    functional. This, therefore involves a diffusible
    protein.
  • B) Observation the cell does not regains
    its function
  • Conclusion the two functional pieces of
    DNA must be adjacent to each other to be
    functional (cis acting),

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BLA OPERON- Control of gene expressing
resistance to Penicillin
  • Usually present on a plasmid in S aureus
  • its function is B-lactam-induced production of
    penicillinase.
  • Bla operon composed of 3 genes
  • blaZ codes for a penicillin-hydrolysing
    enzyme (penicillinase)
  • blaR1 bla l transcription regulator
    genes
  • When penicillin is in the environment,
    membrane-bound signal transducer protein BlaR1
    recognises it and transmits the signal to the
    cytoplasm.
  • Repressor protein Bla I, which binds near to the
    promoter of blaZ preventing its transcription, is
    cleaved off.
  • blaZ is transcribed efficiently to produce
    penicillinase.

65
Negative regulation Substrate induction
66
Positive regulation of the lac operon
67
Positive Gene Regulation
  • In the lac operon there are other molecules to
    further stimulate transcription.
  • Lactose will only be digested for energy when
    there isnt much glucose around
  • When glucose levels are low, level of cAMP
    molecule builds up

68
cAMP and CAP
  • CAP regulatory protein that binds to cAMP
  • CAP is inactive unless cAMP binds to it

69
Positive gene regulation
  • If there isnt much glucose? high levels of cAMP
  • CAP and cAMP bind ? CAP can bind to the promoter
    ? stimulates RNA Polymerase to bind

70
Positive gene regulation
  • When glucose levels rise again, cAMP levels will
    drop ? no longer bound to CAP
  • CAP cant bind to promoter ? transcription slows
    down

71
Positive gene regulation
  • The lac operon is controlled on 2 levels
  • Presence of lactose determines if transcription
    can occur
  • CAP in the active form determines how fast
    transcription occurs

72
Lac Operon
Operon is on and enhanced
Operon is ready to be enhanced but is shut off
73
Lac Operon
Operon is off and un-enhanced
Operon is on but un-enhanced
POWERade is a drink manufactured by The Coca-Cola
Company.
74
Lac Operon
75
Induction by negative or positive control
76
Negative regulation end-product repression
77
Do all operons have operator regions?
  • NO
  • There are some genes that always need to be
    transcribed ? they do not need to have operators
    to regulate them in this manner.
  • Ex. genes that participate in cellular respiration

78
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