| Literature DB >> 18775323 |
Gang Li1, Frederick W Alt, Hwei-Ling Cheng, James W Brush, Peter H Goff, Mike M Murphy, Sonia Franco, Yu Zhang, Shan Zha.
Abstract
Mutations in XLF/Cernunnos (XLF) cause lymphocytopenia in humans, and various studies suggest an XLF role in classical nonhomologous end joining (C-NHEJ). We now find that XLF-deficient mouse embryonic fibroblasts are ionizing radiation (IR) sensitive and severely impaired for ability to support V(D)J recombination. Yet mature lymphocyte numbers in XLF-deficient mice are only modestly decreased. Moreover, XLF-deficient pro-B lines, while IR-sensitive, perform V(D)J recombination at nearly wild-type levels. Correspondingly, XLF/p53-double-deficient mice are not markedly prone to the pro-B lymphomas that occur in previously characterized C-NHEJ/p53-deficient mice; however, like other C-NHEJ/p53-deficient mice, they still develop medulloblastomas. Despite nearly normal V(D)J recombination in developing B cells, XLF-deficient mature B cells are moderately defective for immunoglobulin heavy-chain class switch recombination. Together, our results implicate XLF as a C-NHEJ factor but also indicate that developing mouse lymphocytes harbor cell-type-specific factors/pathways that compensate for the absence of XLF function during V(D)J recombination.Entities:
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Year: 2008 PMID: 18775323 PMCID: PMC2630261 DOI: 10.1016/j.molcel.2008.07.017
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970