Multiple 9-1-1 complexes promote homolog synapsis, DSB repair, and ATR signaling during mammalian meiosis

Author:

Pereira Catalina1ORCID,Arroyo-Martinez Gerardo A1ORCID,Guo Matthew Z1ORCID,Downey Michael S1ORCID,Kelly Emma R2,Grive Kathryn J3,Mahadevaiah Shantha K4,Sims Jennie R5,Faca Vitor M6,Tsai Charlton1,Schiltz Carl J1,Wit Niek7,Jacobs Heinz7,Clark Nathan L8ORCID,Freire Raimundo91011ORCID,Turner James4ORCID,Lyndaker Amy M2,Brieno-Enriquez Miguel A12,Cohen Paula E1ORCID,Smolka Marcus B5ORCID,Weiss Robert S1ORCID

Affiliation:

1. Department of Biomedical Sciences, Cornell University

2. Division of Mathematics and Natural Sciences, Elmira College

3. Department of Obstetrics and Gynecology, Brown University

4. Sex Chromosome Biology Laboratory, The Francis Crick Institute

5. Department of Molecular Biology and Genetics, Weill Institute for Cell and Molecular Biology, Cornell University

6. Department of Biochemistry and Immunology, FMRP, University of São Paulo

7. Division of Immunology, The Netherlands Cancer Institute

8. Department of Human Genetics, University of Utah

9. Unidad de Investigación, Hospital Universitario de Canarias

10. Instituto de Tecnologías Biomédicas, Universidad de La Laguna

11. Universidad Fernando Pessoa Canarias

12. Magee-Womens Research Institute, Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh

Abstract

DNA damage response mechanisms have meiotic roles that ensure successful gamete formation. While completion of meiotic double-strand break (DSB) repair requires the canonical RAD9A-RAD1-HUS1 (9A-1-1) complex, mammalian meiocytes also express RAD9A and HUS1 paralogs, RAD9B and HUS1B, predicted to form alternative 9-1-1 complexes. The RAD1 subunit is shared by all predicted 9-1-1 complexes and localizes to meiotic chromosomes even in the absence of HUS1 and RAD9A. Here, we report that testis-specific disruption of RAD1 in mice resulted in impaired DSB repair, germ cell depletion, and infertility. Unlike Hus1 or Rad9a disruption, Rad1 loss in meiocytes also caused severe defects in homolog synapsis, impaired phosphorylation of ATR targets such as H2AX, CHK1, and HORMAD2, and compromised meiotic sex chromosome inactivation. Together, these results establish critical roles for both canonical and alternative 9-1-1 complexes in meiotic ATR activation and successful prophase I completion.

Funder

National Institutes of Health

National Science Foundation

National Center for Research Resources

European Research Council

Cancer Research UK

Medical Research Council

Wellcome Trust

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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