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The Saccharomyces cerevisiae Chromatin Remodeler Fun30 Regulates DNA End Resection and Checkpoint Deactivation
Author(s) -
Vinay V. Eapen,
Neal Sugawara,
Michael Tsabar,
Wei-Hua Wu,
James E. Haber
Publication year - 2012
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.00566-12
Subject(s) - biology , chromatin , homologous recombination , g2 m dna damage checkpoint , dna damage , histone , nucleosome , saccharomyces cerevisiae , non homologous end joining , dna repair , microbiology and biotechnology , dna , exonuclease , cell cycle checkpoint , cell cycle , yeast , genetics , cell , dna polymerase
Fun30 is a Swi2/Snf2 homolog in budding yeast that has been shown to remodel chromatin bothin vitro andin vivo . We report that Fun30 plays a key role in homologous recombination, by facilitating 5′-to-3′ resection of double-strand break (DSB) ends, apparently by facilitating exonuclease digestion of nucleosome-bound DNA adjacent to the DSB. Fun30 is recruited to an HO endonuclease-induced DSB and acts in both the Exo1-dependent and Sgs1-dependent resection pathways. Deletion ofFUN30 slows the rate of 5′-to-3′ resection from 4 kb/h to about 1.2 kb/h. We also found that the resection rate is reduced by DNA damage-induced phosphorylation of histone H2A-S129 (γ-H2AX) and that Fun30 interacts preferentially with nucleosomes in which H2A-S129 is not phosphorylated. Fun30 is not required for later steps in homologous recombination. Like its homolog Rdh54/Tid1, Fun30 is required to allow the adaptation of DNA damage checkpoint-arrested cells with an unrepaired DSB to resume cell cycle progression.

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