| Literature DB >> 18070917 |
Kwon-Yul Ryu1, Shamim A Sinnar, Laura G Reinholdt, Sergio Vaccari, Susan Hall, Manuel A Garcia, Tatiana S Zaitseva, Donna M Bouley, Kim Boekelheide, Mary Ann Handel, Marco Conti, Ron R Kopito.
Abstract
Ubiquitin is encoded in mice by two polyubiquitin genes, Ubb and Ubc, that are considered to be stress inducible and two constitutively expressed monoubiquitin (Uba) genes. Here we report that targeted disruption of Ubb results in male and female infertility due to failure of germ cells to progress through meiosis I and hypogonadism. In the absence of Ubb, spermatocytes and oocytes arrest during meiotic prophase, before metaphase of the first meiotic division. Although cellular ubiquitin levels are believed to be maintained by a combination of functional redundancy among the four ubiquitin genes, stress inducibility of the two polyubiquitin genes, and ubiquitin recycling by proteasome-associated isopeptidases, our results indicate that ubiquitin is required for and consumed during meiotic progression. The striking similarity of the meiotic phenotype in Ubb(-/-) germ cells to the sporulation defect in fission yeast (Schizosaccharomyces pombe) lacking a polyubiquitin gene suggests that a meiotic role of the polyubiquitin gene has been conserved throughout eukaryotic evolution.Entities:
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Year: 2007 PMID: 18070917 PMCID: PMC2223379 DOI: 10.1128/MCB.01566-07
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272