||V(D)J Recombinase-Mediated Deletion of the 'hprt' Gene in T-Lymphocytes from Adult Humans.
Fuscoe, J. C.;
Zimmerman, L. J.;
Moore, M. M.;
||Health Effects Research Lab., Research Triangle Park, NC. ;Environmental Health Research and Testing, Inc., Research Triangle Park, NC. ;Vermont Univ., Burlington. Genetics Lab.
T-lymphocyte gene rearrangement;
DNA mutational analysis;
Polymerase chain reaction;
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||The hprt T-cell cloning assay allows the detection of mutations occurring in vivo in the hypoxanthine guanine phosphoribosyltransferase (hprt) gene of T-lymphocytes. In the report, we examined a collection of 314 hprt-deficient clones derived from adult humans for evidence that the mutations were caused by the illegitimate activity of V(D)J recombinase by analyzing exons 2+3 deletion mutations. DNA sequence analysis of deletion breakpoint junctions showed that eight of the mutations were the result of V(D)J recombinase activity. The frequency of the recombinase-mediated mutations was similar in the adults and newborns (2-4 x 10 to the power of -7). Unregulated expression of V(D)J recombinase activity may be an important mechanism for genomic rearrangements in the genesis of cancer.
||Pub. in Mutation Research, v283 n1 p13-20 Sep 92. Prepared in cooperation with Environmental Health Research and Testing, Inc., Research Triangle Park, NC., and Vermont Univ., Burlington. Genetics Lab.
|NTIS Title Notes
||Reprint: V(D)J Recombinase-Mediated Deletion of the 'hprt' Gene in T-Lymphocytes from Adult Humans.
||PC A02/MF A01