Literature DB >> 28684602

Pathways and Mechanisms that Prevent Genome Instability in Saccharomyces cerevisiae.

Christopher D Putnam1,2, Richard D Kolodner3,4,5,6.   

Abstract

Genome rearrangements result in mutations that underlie many human diseases, and ongoing genome instability likely contributes to the development of many cancers. The tools for studying genome instability in mammalian cells are limited, whereas model organisms such as Saccharomyces cerevisiae are more amenable to these studies. Here, we discuss the many genetic assays developed to measure the rate of occurrence of Gross Chromosomal Rearrangements (called GCRs) in S. cerevisiae These genetic assays have been used to identify many types of GCRs, including translocations, interstitial deletions, and broken chromosomes healed by de novo telomere addition, and have identified genes that act in the suppression and formation of GCRs. Insights from these studies have contributed to the understanding of pathways and mechanisms that suppress genome instability and how these pathways cooperate with each other. Integrated models for the formation and suppression of GCRs are discussed.
Copyright © 2017 by the Genetics Society of America.

Entities:  

Keywords:  DNA repair; DNA replication; genome rearrangements; telomerase; translocations

Mesh:

Year:  2017        PMID: 28684602      PMCID: PMC5500125          DOI: 10.1534/genetics.112.145805

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  358 in total

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

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Review 8.  Systemic and rapid restructuring of the genome: a new perspective on punctuated equilibrium.

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Journal:  Curr Genet       Date:  2020-11-07       Impact factor: 3.886

9.  Phosphoproteomics reveals a distinctive Mec1/ATR signaling response upon DNA end hyper-resection.

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10.  Fission yeast Rad8/HLTF facilitates Rad52-dependent chromosomal rearrangements through PCNA lysine 107 ubiquitination.

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