4.7 Article

Selective modulation of the functions of a conserved DNA motor by a histone fold complex

Journal

GENES & DEVELOPMENT
Volume 29, Issue 10, Pages 1000-1005

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.259143.115

Keywords

homologous recombination; genome replication; replication fork repair; DNA motor proteins; histone fold proteins; structural maintenance of chromosome proteins

Funding

  1. U.S. National Institutes of Health (NIH) [GM057814, ES007061, ES015632, ES015252]
  2. American Cancer Society grant [RSG-12-013-01-CCG]
  3. Leukemia and Lymphoma Society Scholar Award
  4. Italian Association for Cancer Research (AIRC) [IG 14171]
  5. Fondazione Telethon [GGP12160]
  6. European Research Council [REPSUBREP 242928]
  7. NIH grant [GM080670, GM80600, K99/R00 ES021441, T32 GM008539]

Ask authors/readers for more resources

Budding yeast Mph1 helicase and its orthologs drive multiple DNA transactions. Elucidating the mechanisms that regulate these motor proteins is central to understanding genome maintenance processes. Here, we show that the conserved histone fold MHF complex promotes Mph1-mediated repair of damaged replication forks but does not influence the outcome of DNA double-strand break repair. Mechanistically, scMHF relieves the inhibition imposed by the structural maintenance of chromosome protein Smc5 on Mph1 activities relevant to replication-associated repair through binding to Mph1 but not DNA. Thus, scMHF is a function-specific enhancer of Mph1 that enables flexible response to different genome repair situations.

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