Affiliation:
1. Department of Biochemistry and Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, New York 10016
Abstract
ABSTRACT
The
Saccharomyces cerevisiae
hyperrecombination mutation
hpr1
Δ results in instability of sequences between direct repeats that is dependent on transcription of the repeat. Here it is shown that the
HPR1
gene also functions in plasmid stability in the presence of destabilizing transcription elongation. In the
hpr1
Δ mutant, plasmid instability results from unchecked transcription elongation, which can be suppressed by a strong transcription terminator. The plasmid system has been used to examine in vivo aspects of transcription in the absence of Hpr1p. Nuclear run-on studies suggest that there is an increased RNA polymerase II density in the
hpr1
Δ mutant strain, but this is not accompanied by an increase in accumulation of cytoplasmic mRNA. Suppression of plasmid instability in
hpr1
Δ can also be achieved by high-copy expression of the RNA splicing factor
SUB2
, which has recently been proposed to function in mRNA export, in addition to its role in pre-mRNA splicing. High-copy-number
SUB2
expression is accompanied by an increase in message accumulation from the plasmid, suggesting that the mechanism of suppression by Sub2p involves the formation of mature mRNA. Models for the role of Hpr1p in mature mRNA formation and the cause of plasmid instability in the absence of the Hpr1 protein are discussed.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
5 articles.
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