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Molecular and Cellular Biology, June 2002, p. 4136-4146, Vol. 22, No. 12
0270-7306/02/$04.00+0     DOI: 10.1128/MCB.22.12.4136-4146.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Mutations in DNA Replication Genes Reduce Yeast Life Span

Laura L. Mays Hoopes,1 Martin Budd,2 Wonchae Choe,2 Tao Weitao,2 and Judith L. Campbell2*

Braun Laboratories, California Institute of Technology, Pasadena, California 91125,2 Seaver South Laboratory, Department of Biology and Molecular Biology Program, Pomona College, Claremont, California 917111

Received 21 November 2001/ Returned for modification 4 February 2002/ Accepted 18 March 2002

Surprisingly, the contribution of defects in DNA replication to the determination of yeast life span has never been directly investigated. We show that a replicative yeast helicase/nuclease, encoded by DNA2 and a member of the same helicase subfamily as the RecQ helicases, is required for normal life span. All of the phenotypes of old wild-type cells, for example, extended cell cycle time, age-related transcriptional silencing defects, and nucleolar reorganization, occur after fewer generations in dna2 mutants than in the wild type. In addition, the life span of dna2 mutants is extended by expression of an additional copy of SIR2 or by deletion of FOB1, which also increase wild-type life span. The ribosomal DNA locus and the nucleolus seem to be particularly sensitive to defects in dna2 mutants, although in dna2 mutants extrachromosomal ribosomal circles do not accumulate during the aging of a mother cell. Several other replication mutations, such as rad27{Delta}, encoding the FEN-1 nuclease involved in several aspects of genomic stability, also show premature aging. We propose that replication fork failure due to spontaneous, endogenous DNA damage and attendant genomic instability may contribute to replicative senescence. This may imply that the genomic instability, segmental premature aging symptoms, and cancer predisposition associated with the human RecQ helicase diseases, such as Werner, Bloom, and Rothmund-Thomson syndromes, are also related to replicative stress.

* Corresponding author. Mailing address: Braun Laboratories 147-75, California Institute of Technology, Pasadena, CA 91125. Phone: (626) 395-6053. Fax: (626) 405-9452. E-mail: jcampbel{at}cco.caltech.edu.

Molecular and Cellular Biology, June 2002, p. 4136-4146, Vol. 22, No. 12
0022-538X/02/$04.00+0     DOI: 10.1128/MCB.22.12.4136-4146.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

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