Registration for a live webinar on 'Precision medicine treatment for anticancer drug resistance' is now open.
See webinar detailsWe noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Intro slide
- "Central Dogma" of molecular biology
- Eukaryotic RNA polymerases I, II & III
- Introduction to transcription
- Fundamental questions (1)
- Pol II machinery: Overview of topics (1)
- The RNA polymerase "promoter"
- Pol II machinery: Overview of topics (2)
- Pol II core promoter elements
- CpG islands as "proximal" promoter elements
- Summary: Core promoter elements
- Pol II machinery: Overview of topics (3)
- Enhancer elements
- Enhanceosome
- UAS elements (yeast)
- Silencer elements
- URS elements
- Pol II machinery: Overview of topics (4)
- Discovery of the GTFs (1)
- Discovery of the GTFs (2)
- The GTFs of RNA Polymerase II
- Assembly of the pol II transcription PIC
- The GTFs are loosely analogous to sigma factor
- TFIID
- TBP
- TAFs
- TAF functions
- TFIID: 3D structure
- Class II promoters
- TBP-less TAF complexes
- TLFs
- TFIIA
- TFIIB
- TFIIB: inserts into Pol II active center
- TFIIF
- TFIIE
- TFIIH
- TFIIH
- TFIIH: Clinical importance
- Fundamental questions (2)
- Pol II machinery: Overview of topics (5)
- Pol II
- Yeast Pol II - 3D structure (10 subunit)
- Yeast RNAP II - 12 subunit structure
- A marvellous machine for making messages - A. Klug
- The pol II CTD
- Regulation of the Pol II CTD
- Pol II machinery: Overview of topics (6)
- Pol II transcription cycle
- Scaffold: facilitates reinitiaiton by Pol II
- Fundamental questions (3)
- Activation by "recruitment"
- Fundamental questions (4)
- Transcriptional repression
- Unanswered questions
- The End
Topics Covered
- Core promoters
- Enhancers and silencers
- General transcription factors
- RNAP II
- Mechanism of initiation
- Update interview: RNAP II carboxy-terminal domain (CTD)
- Update interview: mRNA-protein particles (mRNPs)
- Update interview: Nuclear pores
- Update interview: Gene loops
- Update interview: Transcription memory
- Update interview: Transcription re-initiation
Talk Citation
Hampsey, M. (2020, October 14). The RNA polymerase II general transcription machinery [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/FMFO3916.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Michael Hampsey has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Update Available
The speaker addresses developments since the publication of the original talk. We recommend listening to the associated update as well as the lecture.
- Full lecture Duration: 41:00 min
- Update Interview Duration: 8:46 min
A selection of talks on Cell Biology
Transcript
Please wait while the transcript is being prepared...
0:05
Francis Crick defined the so-called Central Dogma of molecular biology namely,
DNA encodes RNA, encodes protein.
The process by which RNA is made from a DNA template is called transcription,
whereas decoding of the RNA,
specifically messenger RNA, to make protein is referred to as translation.
In this talk, I focus on basic aspects of transcription,
specifically transcription of eukaryotic class II genes,
those transcribed by RNA polymerase II.
0:35
To put this into context,
I want to remind you that transcription in
eukaryotic cells is catalyzed by three distinct RNA polymerases;
Pol l, Pol II, and Pol III.
Pol I is dedicated to the synthesis of ribosomal RNA,
except the smallest of them, 5S ribosomal RNA.
Pol II transcribes protein and coding genes to yield
messenger RNA as well as a few small nuclear RNAs,
and Pol III synthesizes transfer RNAs, 5S ribosomal RNA,
and also a few small nuclear RNAs,
whereas only messenger RNA is translated to yield protein.
The ribosomal and transfer RNAs are also
directly involved in protein synthesis by the ribosome.
1:14
In 2001, the complete DNA sequence of the human genome was published,
revealing approximately 30,000 protein encoding genes.
This was an extraordinary achievement,
but like so many scientific milestones,
raised as many questions as were answered.
Notable are the questions of how these 30,000
genes are expressed to affect cell growth and differentiation,
and how expression of these genes is regulated.
1:39
This talk addresses several fundamental questions regarding Pol II transcription.
First, how does Pol II identify a gene?
What are the cis-acting DNA sequences and what are
the transacting proteins that are required for transcription?
Second, how does Pol II initiate transcription?
How do the proteins that are required for initiation
interact with Pol II to promote messenger RNA synthesis?
Third, how is transcription regulated in response to factors that affect gene expression?
Including the physiological and developmental factors to which all cells respond.
I'll revisit these questions as I proceed.
I've organized my presentation of the Pol II machinery into five parts.