Affiliation:
1. Department of Biochemistry and Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, New York 10016
Abstract
ABSTRACT
Multiple genetic pathways have been shown to regulate life span and aging in the yeast
Saccharomyces cerevisiae
. Here we show that loss of a component of the RNA polymerase II complex, Hpr1p, results in a decreased life span. Although
hpr1
Δ mutants have an increased rate of recombination within the ribosomal DNA (rDNA) array, this is not accompanied by an increase in extrachromosomal rDNA circles (ERCs). Analyses of mutants that affect replication of the rDNA array and suppressors that reverse the phenotypes of the
hpr1
Δ mutant show that the reduced life span is associated with increased genomic instability but not with increased ERC formation. The
hpr1
Δ mutant acts in a pathway distinct from previously described mutants that reduce life span.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
54 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献