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Promoters and transcription factors
Context
Transcription -The conversion of DNA information
to RNA information.
Happens before splicing
Mechanism for transcription is RNA polymerase.
Followed by translation - The conversion of RNA
information to amino acid sequence
RNA polymerase
>10
subunits
Several
types I-III
Type
II is involved in "gene" transcription.
Type
I and III transcribe ribosomal and transfer
RNA
Characteristics of transcription
Polymerase
does not recognise its promoter
directly, only through use of promoters can
transcription take place.
TBP (TATA box)
is a common element in
initiation complex but may not bind to a TATA
box in all cases
TBP binds
Several
in the minor groove
other transcription factors must also bind
How transcription elements are
discovered
Use of a reporter system
Procedural, makes the enzyme assay routine
Artifacts present, not all factors will be present
Chop off the DNA until you get a change in the
reporter enzyme levels
Mutate a potential site (Single bp changes)
Consensus sequences
Promoters vs Enhancers
Characteristics of each
Promoters <200 bp from start
Enhancers < 'several kb'
May end up closer due to bending
Typically more global regulatory elements, tissue or time
specific
Enhancers several closely packed sites
Promoters more dispersed
Both consist of < 10 bp elements
Example: CAAT Box
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Sequence is used by alpha globin, adenovirus,
fibrinogen, two proteins from rat liver
Other sequences around CAAT box probably
influence what actually gets bound to the CAAT
box
A conserved DNA element does not necessarily
imply that the same regulatory element is binding.
Enhancers
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Can be either upstream or downstream.
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Could change density of supercoiling.
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Provide an entry site for the polymerase.
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Anchor the DNA at a place within the cell for
access.
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Silencers
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Insulators
Genomic structure
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A obvouly recent field
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Look at the genome anatomy
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Top down look at the problem
TRANSFAC
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Database of transcription factors
Classifed by a system similar to EC number, but
not directly compairable
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Open (to non comerical) and updateable
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Utilized by a variety of tools
Sequence repeats
May have different densities
Called microsatellite DNA
TTAGGG on the ends on chromosome at the telomeres
Transposable elements
35% of human genome is TE
>50% of corn is TE
1.8% of C. elegans is TE
15% of Drosophila is TE
Types of TE's
LTR's (Long terminal repeats)
Retroviruse elements
Short 80-300bp segments SINES
And longer 6-8 kb segments LINES
Psuedogenes
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A snapshot of evolution
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New gene functions gained by gene duplication.
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The duplicated gene is then free to mutate
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processed psudeogenes, no introns or promoter
regions, thought to be due to RT
Synteny
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Fancy word for gene order
The sequence of a gene may change much faster
than the order of the genes
May be a very useful confirmation or hint of the
function of a gene
Operon/clusters
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It is normal for a prokaryote to transcribe clusters
of genes which are translated toghter as well.
May cluster genes working on the same metabolic
process togther
Eukaryotes there is not the co-transcription and
the clustering is not found
Gene order is still very conserved
ACR
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Ancient conserved regions
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20-40% of coding sequences are ACRs
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Possibly represent proteins present at the time of
prokaryotic/eukaryotic split
Horozontal gene transfer
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As opposed to vertical transer (inheritance)
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Mitochondira/Chloroplasts
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Significant in bacteria 12.8% in E. coli