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Transcription termination by nuclear RNA polymerases

descriptionPublicationkeyboard_double_arrow_right Article 01 Jun 2009Publisher:Cold Spring Harbor LaboratoryJournal:Genes & Development, volume 23, pages 1,247-1,269 (issn: 0890-9369, eissn: 1549-5477,

Authors: James L. Manley; Patricia Richard;

doi: 10.1101/gad.1792809

pmid: 19487567

pmc: PMC2763537

Transcription termination by nuclear RNA polymerases

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Abstract

Gene transcription in the cell nucleus is a complex and highly regulated process. Transcription in eukaryotes requires three distinct RNA polymerases, each of which employs its own mechanisms for initiation, elongation, and termination. Termination mechanisms vary considerably, ranging from relatively simple to exceptionally complex. In this review, we describe the present state of knowledge on how each of the three RNA polymerases terminates and how mechanisms are conserved, or vary, from yeast to human.

Related Organizations

King’s University
United States
University of Chicago
United States

Keywords

Cell Nucleus, Transcription, Genetic, Exoribonucleases, Animals, Humans, DNA-Directed RNA Polymerases, Saccharomyces cerevisiae, RNA 3' End Processing, Transcription Factors

46 Research products, page 1 of 5

Protein AIR1
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Protein AIR2
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Cell division control protein 73
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D-3-phosphoglycerate dehydrogenase 1
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Helicase SEN1
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Chromo domain-containing protein 1
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Endoribonuclease YSH1
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RNA polymerase-associated protein RTF1
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rRNA 2'-O-methyltransferase fibrillarin
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	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	282
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	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 10%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Top 1%