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The MMS22L–TONSL heterodimer directly promotes RAD51‐dependent recombination upon replication stress
Author(s) -
Piwko Wojciech,
Mlejnkova Lucie J,
Mutreja Karun,
Ranjha Lepakshi,
Stafa Diana,
Smirnov Alexander,
Brodersen Mia ML,
Zellweger Ralph,
Sturzenegger Andreas,
Janscak Pavel,
Lopes Massimo,
Peter Matthias,
Cejka Petr
Publication year - 2016
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.15252/embj.201593132
Subject(s) - rad51 , biology , homologous recombination , replication protein a , dna replication , microbiology and biotechnology , replication factor c , control of chromosome duplication , origin recognition complex , dna , eukaryotic dna replication , dna binding protein , genetics , gene , transcription factor
Abstract Homologous recombination ( HR ) is a key pathway that repairs DNA double‐strand breaks ( DSB s) and helps to restart stalled or collapsed replication forks. How HR supports replication upon genotoxic stress is not understood. Using in vivo and in vitro approaches, we show that the MMS22L–TONSL heterodimer localizes to replication forks under unperturbed conditions and its recruitment is increased during replication stress in human cells. MMS22L–TONSL associates with replication protein A (RPA)‐coated ssDNA, and the MMS22L subunit directly interacts with the strand exchange protein RAD51. MMS22L is required for proper RAD51 assembly at DNA damage sites in vivo , and HR‐mediated repair of stalled forks is abrogated in cells expressing a MMS22L mutant deficient in RAD51 interaction. Similar to the recombination mediator BRCA2, recombinant MMS22L–TONSL limits the assembly of RAD51 on dsDNA, which stimulates RAD51‐ssDNA nucleoprotein filament formation and RAD51‐dependent strand exchange activity in vitro . Thus, by specifically regulating RAD51 activity at uncoupled replication forks, MMS22L–TONSL stabilizes perturbed replication forks by promoting replication fork reversal and stimulating their HR‐mediated restart in vivo .