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Full-Text Articles in Medicine and Health Sciences
Rad51c Deficiency In Mice Results In Early Prophase I Arrest In Males And Sister Chromatid Separation At Metaphase Ii In Females, Sergey Kuznetsov, Manuela Pellegrini, Kristy Shuda, Oscar Fernandez-Capetillo, Yilun Liu, Betty K. Martin, Sandra Burkett, Eileen Southon, Debananda Pati, Lino Tessarollo, Stephen D. West, Peter J. Donovan, Andre Nussenzweig, Shyam K. Sharan
Rad51c Deficiency In Mice Results In Early Prophase I Arrest In Males And Sister Chromatid Separation At Metaphase Ii In Females, Sergey Kuznetsov, Manuela Pellegrini, Kristy Shuda, Oscar Fernandez-Capetillo, Yilun Liu, Betty K. Martin, Sandra Burkett, Eileen Southon, Debananda Pati, Lino Tessarollo, Stephen D. West, Peter J. Donovan, Andre Nussenzweig, Shyam K. Sharan
Department of Biochemistry and Molecular Biology Faculty Papers
RAD51C is a member of the RecA/RAD51 protein family, which is known to play an important role in DNA repair by homologous recombination. In mice, it is essential for viability. Therefore, we have generated a hypomorphic allele of Rad51c in addition to a null allele. A subset of mice expressing the hypomorphic allele is infertile. This infertility is caused by sexually dimorphic defects in meiotic recombination, revealing its two distinct functions. Spermatocytes undergo a developmental arrest during the early stages of meiotic prophase I, providing evidence for the role of RAD51C in early stages of RAD51-mediated recombination. In contrast, oocytes …