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TFIID and SAGA roles in transcription machinery

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Title: TFIID and SAGA roles in transcription machinery


1
TFIID and SAGA rolesin transcription machinery
Inna WeinerReading group in Computational
Molecular Biology16/11/06
2
Global structure of RNA polymerase II promoters
TSS
3
The core promoter
(Butler and Kadonaga, 2002)
4
How to recruit RNA Polymerase?
Assembly of general transcription factors is
required to recruit RNA Polymerase to promoters
A9.30
5
General transcription factors
  • Factors that permit efficient selective
    initiation by Pol II in vitro
  • Promoters recognition
  • DNA melting
  • Isolated by biochemical fractionation
    experiments.
  • TFIIA, TFIIB, TFIID, TFIIE,TFIIF and TFIIH
    complexes were isolated and are sufficient to
    permit in vitro specific transcription.

6
TBP
  • TATA box - Binding Protein
  • TBP is a single polypeptide that sits astride
    the TATA box as a molecular ''saddle,'' inducing
    a sharp bend in the DNA
  • Regarded as a universal transcription factor,
    essential for initiation by RNA Pol I, II, and III

7
TAFs (TBP Associated Factors)
  • The role of the TAFs in the TFIID complex
  • - Specific interactions with activators
  • - Binding to the promoter Inr and DPE elements
  • - Modifying chromatin

8
Pre Initiation Complex (PIC) formation
Transition from PIC formation into active
transcription 1. Initiation one of TFIIH
subunits has an helicase activity and is able to
melt the double helices DNA. 2. Elongation this
step is triggered by the phosphorilation of the
CTD repeats of the polymerase by one of the TFIIH
subunit that has a kinase activity.
9
Pol II starts mRNA synthesis
Very few factors accompany the elongating
transcript
10
Summary
Localization to promoters
Melting the DNA, transcription initiation and
elongation
11
Is the general transcription machinery really
general?
(Holstege et al., 1998)
12
Outline
  • Introduction to general transcription machinery
  • TFIID and SAGA unique or redundant function?
  • TFIID and SAGA roles in transcription regulation

13
(No Transcript)
14
TFIID and SAGA
  • Multi-unit complexes
  • Perform two actions essential for Pol II
    initiation
  • Contain a subunit with histone acetyltransferase
    activity
  • Possess TBP binding activity
  • Question

Are the functions of TFIID and SAGA in vivo
unique or overlapping?
15
Percentage of genome dependent on subunits of
SAGA and TFIID
16
Whole genome analysis of shared TAFIIs mutations
17
Shared vs Specific TAFIIs Influence
30 of the genome is dependent on TFIID specific
sub-units 12 of the genome is dependent on SAGA
specific sub-units
70 of the genome depends on one or more of the
shared TAFs
18
How do TFIID and SAGA interact?
TFIID and SAGA have compensatory functions
19
Genetic Interactions
Aggravating interaction
Alleviating interaction
No interaction
Slide by Ariel
20
How do TFIID and SAGA interact?
TFIID and SAGA have compensatory functions
21
Conclusions
  • There are distinct requirements for specific
    sub-units of TFIID and SAGA in global expression
  • The functions of TAFII145 and GCN5 are redundant

22
Improvements
  • Statistical test instead of 2-fold
  • Check which genes respond to each element
    deletion?
  • Define environmental changes

23
(No Transcript)
24
Research Objective
  • TFIID and SAGA
  • Share a common set of TAFs
  • Regulate chromatin
  • Deliver TBP to promoters
  • What is their distinct function and relationship
    in genome-wide regulatory network?
  • Tested organism S.cerevisiae

25
Experimental Setup
  • Create single and double-mutants
  • SAGA-specific mutant GCN5, SPT3
  • TFIID-specific mutant TAF1 (TAFII145)
  • Compare gene expression of single and double
    mutants by performing high-throughput analysis

26
GCN5 mutants
  • gcn5? strain displayed a general decrease in
    expression
  • Over 60 of the genes decreased expression by gt4
    standard devations
  • Gcn5hat did not change expression significantly

? GCN5 makes a positive modest contribution to
the expression of most of the genes ? HAT
activity of GCN5 plays a redundant or minor role
  • rbp1-1 gene expression without pol II activity

27
SPT3 mutants and TAF1 mutants
  • spt3? and spt3E240K strains do not differ
    substantially from wild type

? spt3 plays a small or redundant role
  • Taf1ts2 strain causes leftward shift of the
    distribution
  • 84 of the genome decreased depression by gt4
    stds
  • But population shift is not as severe as for
    rbp1-1

? taf1 makes a positive contribution to genes
expression, but its action is not absolute
28
GCN5/TAF1 double mutants
  • TAF1/GCN5 double mutants shift the population
    like rbp1-1
  • TAF1 and GCN5? interaction is expected
  • GCN5hat sensitivity suggests that HAT activity of
    GCN5 is important when TAF1 is absent

? GCN5 makes a positive modest contribution to
the expression of most of the genes ? HAT
activity of GCN5 plays a redundant or minor role
? GCN5 and TAF1 are associated to the same HAT
activity
29
SPT3 mutants and TAF1 mutants
? spt3 plays a small or redundant role
  • 97 of genes in the TAF1/SPT3? mutant decreased
    by gt4 stds nearly complete shutdown of
    transcription

? both TAF1 and SPT3 contribute to the expression
of all measurable genes ? SAGA and TFIID are the
only redundant complexes in transcriptional
general activity
? taf1 makes a positive contribution to genes
expression, but its action is not absolute
30
Conclusions
  1. TFIID and SAGA each contribute to the expression
    of nearly all genes

31
TFIID or SAGA dominated genes
  • TFIID-dominated genes 90 that showed greater
    dependency on TAF1 than SPT3
  • SAGA-dominated genes 10 that are SPT3-dependent
  • TAF1 appears to be inactive in SAGA-dominated
    genes

32
Conclusions
  1. TFIID and SAGA each contribute to the expression
    of nearly all genes
  2. TFIID dominates at 90 of all genes, and SAGA
    Dominates at 10

33
Stress-Induced Genes Tend to be SAGA Dominated
  • Enrichment in stress-dependent conditions
  • Genes that are commonly upregulated biased
    (p_value lt 10-30) to SAGA-dominated
  • Genes that are commonly downregulated biased
    (p_value lt 10-10) to TFIID-dominated
  • What advantage might SAGA provide in
    environmental stress response that TFIID does not?

34
Conclusions
  • TFIID and SAGA each contribute to the expression
    of nearly all genes

SAGA TFIID
10 90
Stress-Induced Stress-Repressed


35
Histone Acetylation
  • Acetylation of H3 and H4 is associated with
    transcriptional activation
  • H4 under-acetylated regions were biased to
    SAGA-dominated genes whereas H4 overacetylated
    regions biased to TFIID-dominated genes
  • Hda1 and Rpd3 appear to assist in keeping low
    acetylation at SAGA-dominated genes and high
    acetylation at TFIID-dominated genes

36
Conclusions
  • TFIID and SAGA each contribute to the expression
    of nearly all genes

SAGA TFIID
10 90
Stress-Induced Stress-Repressed
H4 high acetylation pattern Low stress

37
SAGA-dominated genes are largely TAF-independent
  • TAFs (TBP Associated Factors) are subunits of
    TFIID but a subset are also present in SAGA
  • Genes that are positively regulated by TAFs were
    biased toward the TFIID-dominated class
  • TAF-independent promoters are
    likely to be
    SAGA-dominated

38
SAGA-dominated genes are highly regulated
  • How do other transcription factors function?
  • SRB10 phosphorilates a number of stress response
    regulators. Genes that are most inhibited by
    SRB10 are SAGA-dominated
  • Genes regulated by stress activators Msn2 and
    Msn4 are also SAGA-dominated

?There is a coordinated stress response pathway
that is up-regulated by gene-specific activators
like Msn2/4 and down-regulated by Srb-10 -
regulated phosphorylation and histone
de-acetylation
39
SAGA-dominated genes are Coordinately Regulated
Stress-induced gened
40
Summary
  • TFIID and SAGA each contribute to the expression
    of nearly all genes

SAGA-dominated genes TFIID-dominated genes
10 90
Stress-Induced Stress-Repressed
H4 high acetylation pattern Low stress
Coordinately and tightly regulated TAF-dependent
41
Two distinct mechanisms
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