Gene function prediction from congruent synthetic lethal interactions in yeast

Mol Syst Biol. 2005:1:2005.0026. doi: 10.1038/msb4100034. Epub 2005 Nov 22.

Abstract

We predicted gene function using synthetic lethal genetic interactions between null alleles in Saccharomyces cerevisiae. Phenotypic and protein interaction data indicate that synthetic lethal gene pairs function in parallel or compensating pathways. Congruent gene pairs, defined as sharing synthetic lethal partners, are in single pathway branches. We predicted benomyl sensitivity and nuclear migration defects using congruence; these phenotypes were uncorrelated with direct synthetic lethality. We also predicted YLL049W as a new member of the dynein-dynactin pathway and provided new supporting experimental evidence. We performed synthetic lethal screens of the parallel mitotic exit network (MEN) and Cdc14 early anaphase release pathways required for late cell cycle. Synthetic lethal interactions bridged genes in these pathways, and high congruence linked genes within each pathway. Synthetic lethal interactions between MEN and all components of the Sin3/Rpd3 histone deacetylase revealed a novel function for Sin3/Rpd3 in promoting mitotic exit in parallel to MEN. These in silico methods can predict phenotypes and gene functions and are applicable to genomic synthetic lethality screens in yeast and analogous RNA interference screens in metazoans.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Benomyl / pharmacology
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / physiology
  • Drug Resistance, Fungal
  • Genes, Fungal / physiology*
  • Histone Deacetylases / genetics
  • Histone Deacetylases / physiology
  • Microtubules / physiology
  • Mitosis / physiology
  • Models, Biological
  • Phenotype
  • Protein Tyrosine Phosphatases / genetics
  • Protein Tyrosine Phosphatases / physiology
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / physiology*
  • Transcription Factors / genetics
  • Transcription Factors / physiology

Substances

  • CDC14 protein, S cerevisiae
  • Cell Cycle Proteins
  • Repressor Proteins
  • SIN3 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • YLL049W protein, S cerevisiae
  • Protein Tyrosine Phosphatases
  • RPD3 protein, S cerevisiae
  • Histone Deacetylases
  • Benomyl