The human gene XPC (formerly designated XPCC), which corrects the repa
ir deficiency of xeroderma pigmentosum (XP) group C cells, was mapped
to 3p25. A cDNA probe for Southern blot hybridization and diagnostic P
CR analyses of hybrid clone panels informative for human chromosomes i
n general and portions of chromosome 3 in particular produced the init
ial results. Fluorescence in situ hybridization utilizing both a yeast
artificial chromosome DNA containing the gene and XPC cDNA as probes
provided verification and specific regional assignment. A conflicting
assignment of XPC to chromosome 5 is discussed in Light of inadequacie
s in the exclusive use of microcell-mediated chromosome transfer for g
ene mapping. (C) 1994 Academic Press, Inc.