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Essential Saccharomyces cerevisiae genome instability suppressing genes identify potential human tumor suppressors.


ABSTRACT: Gross Chromosomal Rearrangements (GCRs) play an important role in human diseases, including cancer. Although most of the nonessential Genome Instability Suppressing (GIS) genes in Saccharomyces cerevisiae are known, the essential genes in which mutations can cause increased GCR rates are not well understood. Here 2 S. cerevisiae GCR assays were used to screen a targeted collection of temperature-sensitive mutants to identify mutations that caused increased GCR rates. This identified 94 essential GIS (eGIS) genes in which mutations cause increased GCR rates and 38 candidate eGIS genes that encode eGIS1 protein-interacting or family member proteins. Analysis of TCGA data using the human genes predicted to encode the proteins and protein complexes implicated by the S. cerevisiae eGIS genes revealed a significant enrichment of mutations affecting predicted human eGIS genes in 10 of the 16 cancers analyzed.

SUBMITTER: Srivatsan A 

PROVIDER: S-EPMC6717276 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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Essential <i>Saccharomyces cerevisiae</i> genome instability suppressing genes identify potential human tumor suppressors.

Srivatsan Anjana A   Li Binzhong B   Sanchez Dafne N DN   Somach Steven B SB   da Silva Vandeclecio L VL   de Souza Sandro J SJ   Putnam Christopher D CD   Kolodner Richard D RD  

Proceedings of the National Academy of Sciences of the United States of America 20190813 35


Gross Chromosomal Rearrangements (GCRs) play an important role in human diseases, including cancer. Although most of the nonessential Genome Instability Suppressing (GIS) genes in <i>Saccharomyces cerevisiae</i> are known, the essential genes in which mutations can cause increased GCR rates are not well understood. Here 2 <i>S. cerevisiae</i> GCR assays were used to screen a targeted collection of temperature-sensitive mutants to identify mutations that caused increased GCR rates. This identifie  ...[more]

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