Abstract
Sister-chromatid cohesion, established during replication by the protein complex cohesin, is essential for both chromosome segregation and double-strand break (DSB) repair. Normally, cohesion formation is strictly limited to the S phase of the cell cycle, but DSBs can trigger cohesion also after DNA replication has been completed. The function of this damage-induced cohesion remains unknown. In this investigation, we show that damage-induced cohesion is essential for repair in postreplicative cells in yeast. Furthermore, it is established genome-wide after induction of a single DSB, and it is controlled by the DNA damage response and cohesin-regulating factors. We thus define a cohesion establishment pathway that is independent of DNA duplication and acts together with cohesion formed during replication in sister chromatid-based DSB repair.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetyltransferases / genetics
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Acetyltransferases / metabolism
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Cell Cycle Proteins / metabolism
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Cell Division
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Chromatids / physiology*
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Chromosomal Proteins, Non-Histone / metabolism
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Cohesins
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DNA Breaks, Double-Stranded*
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DNA Repair*
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DNA Replication
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DNA, Fungal / biosynthesis
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DNA, Fungal / metabolism*
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G2 Phase
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Genome, Fungal
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Intracellular Signaling Peptides and Proteins
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Mutation
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism
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Protein Serine-Threonine Kinases
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / metabolism
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Saccharomyces cerevisiae / physiology*
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Saccharomyces cerevisiae Proteins / genetics
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Saccharomyces cerevisiae Proteins / metabolism
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Signal Transduction
Substances
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Cell Cycle Proteins
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Chromosomal Proteins, Non-Histone
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DNA, Fungal
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Intracellular Signaling Peptides and Proteins
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Nuclear Proteins
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Saccharomyces cerevisiae Proteins
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Acetyltransferases
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ECO1 protein, S cerevisiae
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MEC1 protein, S cerevisiae
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Protein Serine-Threonine Kinases