- THIS ARTICLE
- Full Text
- Full Text (PDF)
-
All Versions of this Article:
genetics.106.059311v1
174/1/519 most recent - Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Email this article to a friend
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Heck, J. A.
- Articles by Alani, E.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Heck, J. A.
- Articles by Alani, E.
Originally published as Genetics Published Articles Ahead of Print on July 2, 2006.
Genetics, Vol. 174, 519-523, September 2006, Copyright © 2006
doi:10.1534/genetics.106.059311
Accumulation of Recessive Lethal Mutations in Saccharomyces cerevisiae mlh1 Mismatch Repair Mutants Is Not Associated With Gross Chromosomal Rearrangements
Julie Akiko Heck*,
David Gresham
,
David Botstein
and
Eric Alani*,1
* Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York 14853 and
Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544
1 Corresponding author: Department of Molecular Biology and Genetics, Cornell University, 459 Biotechnology Bldg., Ithaca, NY 14853-2703.
E-mail: eea3{at}cornell.edu
We examined mismatch repair (MMR)-defective diploid strains of budding yeast grown for
160 generations to determine whether decreases in spore viability due to the uncovering of recessive lethal mutations correlated with an increase in gross chromosomal rearrangements (GCRs). No GCRs were detected despite dramatic decreases in spore viability, suggesting that frameshift and/or other unrepaired DNA replication lesions play a greater role than chromosomal instability in decreasing viability in MMR-defective strains.