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Printable Handouts
Navigable Slide Index
- Introduction
- Talk outline
- Bacterial sigma factors
- RNA polymerase holoenzymes
- Properties of sigma54
- Domains of sigma54
- Activators of sigma54 holoenzyme
- The transcription activator protein PspF
- Bacterial enhancer binding proteins
- Properties of EBPS
- Domain organisation of EBPS
- Features of EBPs
- The transcription activator protein PspF
- Binding interactions between sigma54 and EBP
- Model of EBP action
- Cryo-electron microscopy 3D reconstruction
- Model of intermediate complex
- Interactions at promoter
- Promoter DNA proximities
- Cryo-EM complex
- Differences between NTRC1 and PspF
- Changes occurred in the nucleotide binding pocket
- Proposed movements of L1 and L2
- Proposed conformational signalling pathway
- Structures of PspF AAA domain (< 2A)
- Structural features of EBP AAA domain
- RMSD plots of PspF +/- nucleotide
- Nucleotide binding pocket
- Features of pocket
- Bound nucleotide
- Nucleotide binding pocket with magnesium
- Nucleotide driven switch
- Nucleotide communication to L1 and L2
- Nucleotide states and binding sigma54
- The switch and asparagine 64
- EBPS as AAA proteins
- A conserved switch
- Conformational change cycle
- Mechanism of EBP
- Summary
- Sigma54 exerts a tight inhibition on RNAP
- Crystal structure of RNAP-sigma54
- Sigma54 structure and functional domains
- Overlay with transcription bubble
- RI/RIII-ELH-HTH
- RII/RIII-CBD
- Acknowledgements
- References
Topics Covered
- Understanding the origins of nucleotide driven conformational change
- Molecular motors powered by ATP
- ATPases belonging to the AAA protein family
- PspF from E.coli
- Phage shock genes
- ATP transition state analogue ADPAlF
- X-ray crystallographic structural analysis
- Initiation of conformational changes
- Role of structural changes in sigma54 subunit
- Formation of open promoter complexes
- Changes in DNA binding properties of sigma54
- Structural organisation of the RNAP holoenzyme
Talk Citation
Buck, M. (2016, December 29). Nucleotide dependent functioning of bacterial enhancer binding proteins, activators of sigma54 RNA polymerase [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/RBSL8466.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Martin Buck has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Nucleotide dependent functioning of bacterial enhancer binding proteins, activators of sigma54 RNA polymerase
A selection of talks on Cell Biology
Transcript
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0:00
Over the next 40 minutes or so,
I'd like to describe
our current understanding
of how nucleotide-dependent
transcription operates.
0:12
I would describe
how one major variant sigma factor,
an RNA polymerase subunit participates
in this process
of transcriptional activation.
I'll describe in detail its activators
and in particular
I will describe how nucleotide,
in particular ATP,
causes changes
in the transcriptional activator.
And that will be based on
recent structural studies
on a transcriptional activator from E. coli,
the so-called phage shock protein F, PspF,
an E. coli transcriptional activator.
0:43
Bacteria use proteins called sigma factors
to bring RNA polymerase to the promoter DNA.
Typically, they exist in two classes,
the sigma70 class
which is well represented
with many members.
Here we see in E. coli
there are one, two, three, four, five,
six members of the sigma70 class.
The focus of my talk
is on an alternative sigma factor
called sigma54, it's got a single member.
Sometimes, it's only one of
only two sigma factors in bacteria,
and it really provides an example
of a transcriptional activation mechanism
that resembles eukaryotic enhancer-dependent
transcriptional activation.
1:22
Here we see the organization in E. coli
of the RNA polymerase sigma relationship.
The sigma70 type factors
combine with the core RNA polymerase
to form a sigma70 type holoenzyme.
The sigma54 factor
combines with the same core enzyme
to form the sigma54
RNA polymerase holoenzyme.
The important point here
is that the sigma54
containing RNA polymerase
has got very, very different requirements
to initiate transcription
compared to the sigma70 RNA polymerase.
In particular,
sigma54 RNA polymerase requires
the use of ATP hydrolysis
to drive the formation
of the DNA melting step in transcription.
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