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PMID: 6251092 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Transcription and in vitro processing of yeast 5 S rRNA.

The Journal of biological chemistry ·Vol. 255 ·No. 19 ·1980-10-10 ·Pages 9501-6

Tekamp PA, Garcea RL, Rutter WJ

Abstract

A method is described for the isolation of a yeast chromatin fraction highly enriched in ribosomal DNA sequences. In the presence of exogenous yeast RNA polymerase III, this purified chromatin actively synthesizes a set of 5 S ribosomal RNAs all of which have 5'-sequences identical with mature 5 S RNA but which end with a variable number (up to 10) of additional residues at the 3'-terminus. These extra nucleotides are precisely removed by a processing nuclease found in the chromatin supernatant fraction.

MeSH Terms
Base Sequence Chromatin/metabolism DNA Restriction Enzymes DNA-Directed RNA Polymerases/metabolism Genetic Code Kinetics Molecular Weight Oligoribonucleotides/analysis Protein Biosynthesis RNA, Ribosomal/biosynthesis Ribonuclease T1 Saccharomyces cerevisiae/metabolism Transcription, Genetic
Chemicals
Chromatin Oligoribonucleotides RNA, Ribosomal DNA-Directed RNA Polymerases DNA Restriction Enzymes Ribonuclease T1
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tekamp P A
Garcea R L
Rutter W J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1980-10-10
Pages
9501-6
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM 21830 · United States
NIGMS NIH HHS · GM 25157 · United States
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