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Visual Analysis of the Yeast 5S rRNA Gene Transcriptome: Regulation and Role of La Protein
Author(s) -
Sarah L. French,
Yvonne N. Osheim,
David A. Schneider,
Martha L. Sikes,
César Fernández Fernández,
Laura A. Copela,
Vikram Misra,
Michio Nomura,
Sandra L. Wolin,
Ann L. Beyer
Publication year - 2008
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00127-08
Subject(s) - biology , transcriptome , genetics , gene , yeast , computational biology , regulation of gene expression , gene expression
5S rRNA genes fromSaccharomyces cerevisiae were examined by Miller chromatin spreading, representing the first quantitative analysis of RNA polymerase III genes in situ by electron microscopy. These very short genes, ∼132 nucleotides (nt), were engaged by one to three RNA polymerases. Analysis in different growth conditions and in strains with a fourfold range in gene copy number revealed regulation at two levels: number of active genes and polymerase loading per gene. Repressive growth conditions (presence of rapamycin or postexponential growth) led first to fewer active genes, followed by lower polymerase loading per active gene. The polymerase III elongation rate was estimated to be in the range of 60 to 75 nt/s, with a reinitiation interval of ∼1.2 s. The yeast La protein, Lhp1, was associated with 5S genes. Its absence had no discernible effect on the amount or size of 5S RNA produced yet resulted in more polymerases per gene on average, consistent with a non-rate-limiting role for Lhp1 in a process such as polymerase release/recycling upon transcription termination.

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