Visual Analysis of the Yeast 5S rRNA Gene Transcriptome: Regulation and Role of La Protein

Author:

French Sarah L.1,Osheim Yvonne N.1,Schneider David A.2,Sikes Martha L.1,Fernandez Cesar F.3,Copela Laura A.3,Misra Vikram A.4,Nomura Masayasu2,Wolin Sandra L.3,Beyer Ann L.1

Affiliation:

1. Department of Microbiology, University of Virginia, Charlottesville, Virginia 22908

2. Department of Biological Chemistry, University of California—Irvine, Irvine, California 92697

3. Departments of Cell Biology and Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, Connecticut 06536

4. Departments of Biochemistry and Mathematics, University of Maryland Baltimore County, Baltimore, Maryland 21250

Abstract

ABSTRACT 5S rRNA genes from Saccharomyces 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.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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