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PMID: 3304659 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Functional redundancy and structural polymorphism in the large subunit of RNA polymerase II.

Cell ·Vol. 50 ·No. 6 ·1987-09-11 ·Pages 909-15

Nonet M, Sweetser D, Young RA

Abstract

The RNA polymerase II large subunit contains tandem copies of the sequence Pro Thr Ser Pro Ser Tyr Ser at its carboxyl terminus, the number of which varies from 26 in yeast to 52 in mice. Our results indicate that the heptapeptide repeat sequence is unique and essential to RNA polymerase II. We have determined that a portion of the heptapeptide repeat domain is essential for viability by constructing and analyzing unidirectional deletions of the carboxy-terminal coding sequence in yeast. Cells containing an RNA polymerase II large subunit with less than 10 complete heptapeptide repeats are inviable, those containing 10-12 complete repeats are conditionally viable, and those with 13 or more complete repeats are unconditionally viable. The inviable deletion mutants studied here have truncated RNA polymerase subunits that are stable, but functionally deficient. Finally, the number of repeat units is polymorphic in wild-type yeast strains. These results have implications for the function of this unusual sequence in transcription.

MeSH Terms
Amino Acid Sequence Base Sequence Fungal Proteins/genetics,physiology Polymorphism, Genetic Protein Conformation RNA Polymerase II/genetics,physiology Repetitive Sequences, Nucleic Acid Saccharomyces cerevisiae/enzymology,genetics Transcription, Genetic
Chemicals
Fungal Proteins RNA Polymerase II
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nonet M
Sweetser D
Young R A
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1987-09-11
Pages
909-15
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM34365 · United States
Databases
GENBANK
M17420
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