Pacheco, SaraiMaldonado-Linares, AndrosMarcet-Ortega, MarinaRojas, CristinaMartínez-Marchal, AnaFuentes-Lazaro, JuditLange, JulianJasin, MariaKeeney, ScottFernandez-Capetillo, OscarGarcia-Caldés, MontserratRoig, Ignasi2019-09-162019-09-162018-07-05Nat Commun. 2018;9(1):2622.2041-1723http://hdl.handle.net/20.500.12105/8349Precise execution of recombination during meiosis is essential for forming chromosomally-balanced gametes. Meiotic recombination initiates with the formation and resection of DNA double-strand breaks (DSBs). Cellular responses to meiotic DSBs are critical for efficient repair and quality control, but molecular features of these remain poorly understood, particularly in mammals. Here we report that the DNA damage response protein kinase ATR is crucial for meiotic recombination and completion of meiotic prophase in mice. Using a hypomorphic Atr mutation and pharmacological inhibition of ATR in vivo and in cultured spermatocytes, we show that ATR, through its effector kinase CHK1, promotes efficient RAD51 and DMC1 assembly at RPA-coated resected DSB sites and establishment of interhomolog connections during meiosis. Furthermore, our findings suggest that ATR promotes local accumulation of recombination markers on unsynapsed axes during meiotic prophase to favor homologous chromosome synapsis. These data reveal that ATR plays multiple roles in mammalian meiotic recombination.engVoRhttp://creativecommons.org/licenses/by-nc-sa/4.0/AnimalsAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsCheckpoint Kinase 1Chromosome PairingIn Situ Hybridization, FluorescenceMaleMeiosisMice, 129 StrainMice, Inbred C57BLMice, KnockoutNuclear ProteinsRad51 RecombinaseSpermatocytesTestisDNA Breaks, Double-StrandedHomologous RecombinationAtribución-NoComercial-CompartirIgual 4.0 Internacional2997702791262210.1038/s41467-018-04851-z2041-1723Nature communicationsopen access