Three genetic complementation groups of rodent cells are defective for
both repair of x-ray-induced double-strand breaks and V(D)J recombina
tion. Cells from one group lack a DNA end-binding activity that is bio
chemically and antigenically similar to the Ku autoantigen. Transfecti
on of complementary DNA (cDNA) that encoded the 86-kilodalton subunit
of Ku rescued these mutant cells for DNA end-binding activity, x-ray r
esistance, and V(D)J recombination activity. These results establish a
role for Ku in DNA repair and recombination. Furthermore, as a compon
ent of a DNA-dependent protein kinase, Ku may initiate a signaling pat
hway induced by DNA damage.