A Critical Role for DNA End-Joining Proteins in Both Lymphogenesis and Neurogenesis

XRCC4 was identified via a complementation cloning method that employed an ionizing radiation (IR)-sensitive hamster cell line. By gene-targeted mutation, we show that XRCC4 deficiency in primary murine cells causes growth defects, premature senescence, IR sensitivity, and inability to support V(D)J...

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Published in:Cell Vol. 95; no. 7; pp. 891 - 902
Main Authors: Gao, Yijie, Sun, Yi, Frank, Karen M., Dikkes, Pieter, Fujiwara, Yuko, Seidl, Katherine J., Sekiguchi, JoAnn M., Rathbun, Gary A., Swat, Wojciech, Wang, Jiyang, Bronson, Roderick T., Malynn, Barbara A., Bryans, Margaret, Zhu, Chengming, Chaudhuri, Jayanta, Davidson, Laurie, Ferrini, Roger, Stamato, Thomas, Orkin, Stuart H., Greenberg, Michael E., Alt, Frederick W.
Format: Journal Article
Language:English
Published: United States Elsevier Inc 23-12-1998
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Summary:XRCC4 was identified via a complementation cloning method that employed an ionizing radiation (IR)-sensitive hamster cell line. By gene-targeted mutation, we show that XRCC4 deficiency in primary murine cells causes growth defects, premature senescence, IR sensitivity, and inability to support V(D)J recombination. In mice, XRCC4 deficiency causes late embryonic lethality accompanied by defective lymphogenesis and defective neurogenesis manifested by extensive apoptotic death of newly generated postmitotic neuronal cells. We find similar neuronal developmental defects in embryos that lack DNA ligase IV, an XRCC4-associated protein. Our findings demonstrate that differentiating lymphocytes and neurons strictly require the XRCC4 and DNA ligase IV end-joining proteins and point to the general stage of neuronal development in which these proteins are necessary.
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ISSN:0092-8674
1097-4172
DOI:10.1016/S0092-8674(00)81714-6