About Us |
PMID | 28178517 |
Gene Name | RAD51 |
Condition | Spermatogenesis impairement, Male infertility |
Association |
Associated |
Sex | Male |
Infertility type | Male infertility |
Other associated phenotypes |
Spermatogenesis impairement, Male infertility |
Meiotic Knockdown and Complementation Reveals Essential Role of RAD51 in Mouse Spermatogenesis Dai J, Voloshin O, Potapova S, Camerini-Otero RD. Meiotic homologous recombination (HR) is important for proper chromosomal segregation during gametogenesis and facilitates evolutionary adaptation via genomic reshuffling. In most eukaryotes, HR is mediated by two recombinases, the ubiquitous RAD51 and the meiosis-specific DMC1. The role of RAD51 in mammalian meiosis is unclear and study of its function is limited due to embryonic lethality of RAD51 knockouts. Here, we developed an in vivo meiotic knockdown and protein complementation system to study RAD51 during mouse spermatogenesis. We show that RAD51 is crucial during meiotic prophase and its loss leads to depletion of late prophase I spermatocytes through a p53-dependent apoptotic pathway. This phenotype is distinct from that observed in the DMC1 knockdown. Our meiotic knockdown and complementation system establishes an experimental platform for mechanistic studies of meiotic proteins with unknown functions or essential genes for which a testis-specific knockout is not possible. CI - Published by Elsevier Inc. FAU - Dai, Jieqiong AU - Dai J AD - Genetics and Biochemistry Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892, USA. FAU - Voloshin, Oleg AU - Voloshin O AD - Genetics and Biochemistry Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892, USA. FAU - Potapova, Svetlana AU - Potapova S AD - Division of Intramural Research, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892, USA. |