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PMID: 7739552 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Synthetic lethality of sep1 (xrn1) ski2 and sep1 (xrn1) ski3 mutants of Saccharomyces cerevisiae is independent of killer virus and suggests a general role for these genes in translation control.

Molecular and cellular biology ·Vol. 15 ·No. 5 ·1995-05-00 ·Pages 2719-27

Johnson AW, Kolodner RD

Abstract

Strand exchange protein 1 (Sep1) (also referred to as exoribonuclease I [Xrn1]) from Saccharomyces cerevisiae has been implicated in DNA recombination, RNA turnover, karyogamy, and G4 DNA pairing among other disparate cellular processes. Using a genetic approach to study the role of SEP1/XRN1 in mitotic yeast cells, we identified mutations in the genes superkiller 2 (SKI2) and superkiller 3 (SKI3) as synthetically lethal with an sep1 null mutation. The SKI genes are thought to comprise an intracellular antiviral system controlling the expression of killer toxin from double-stranded RNA virus found in many yeast strains. However, the lethality of sep1 ski2 and sep1 ski3 mutants was independent of the L-A and M viruses, suggesting that the SKI genes act in a general cellular process in addition to virus control. We propose that Sep1/Xrn1 and Ski2 both act to block translation on transcripts targeted for degradation. Using a temperature-sensitive allele of SEP1/XRN1, we show that double mutants display a synthetic cell cycle arrest in late G1 at Start.

Related Genes
MeSH Terms
Base Sequence DNA Primers/genetics DNA, Fungal/genetics Deoxyribonucleases/genetics Exoribonucleases Fungal Proteins/genetics G1 Phase/genetics Genes, Fungal Genes, Lethal Molecular Sequence Data Mutation Phenotype Protein Biosynthesis Saccharomyces cerevisiae/cytology,genetics,virology Saccharomyces cerevisiae Proteins
Chemicals
DNA Primers DNA, Fungal Fungal Proteins SKI2 protein, S cerevisiae Saccharomyces cerevisiae Proteins Deoxyribonucleases Exoribonucleases XRN1 protein, S cerevisiae
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Johnson A W
Division of Cellular and Molecular Biology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Kolodner R D
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1995-05-00
Pages
2719-27
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC230502
Subset
IM
Grants
NCI NIH HHS · CA06516 · United States
NIGMS NIH HHS · GM13594 · United States
NIGMS NIH HHS · GM29383 · United States
Analysis Services
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