Grawunder U, Zimmer D, Fugmann S, Schwarz K, Lieber M R
University of Southern California School of Medicine, Norris Comprehensive Cancer Center, Department of Pathology, Los Angeles 90033, USA.
Mol Cell. 1998 Oct;2(4):477-84. doi: 10.1016/s1097-2765(00)80147-1.
Nonhomologous DNA end joining (NHEJ) is the major pathway for repairing double-strand DNA breaks. V(D)J recombination is a double-strand DNA breakage and rejoining process that relies on NHEJ for the joining steps. Here we show that the targeted disruption of both DNA ligase IV alleles in a human pre-B cell line renders the cells sensitive to ionizing radiation and ablates V(D)J recombination. This phenotype can only be reversed by complementation with DNA ligase IV but not by expression of either of the remaining two ligases, DNA ligase I or III. Hence, DNA ligase IV is the activity responsible for the ligation step in NHEJ and in V(D)J recombination.
非同源DNA末端连接(NHEJ)是修复双链DNA断裂的主要途径。V(D)J重组是一个双链DNA断裂和重新连接的过程,其连接步骤依赖于NHEJ。我们在此表明,在人前B细胞系中对两个DNA连接酶IV等位基因进行靶向破坏会使细胞对电离辐射敏感,并消除V(D)J重组。这种表型只能通过用DNA连接酶IV互补来逆转,而不能通过其余两种连接酶DNA连接酶I或III中的任何一种的表达来逆转。因此,DNA连接酶IV是负责NHEJ和V(D)J重组中连接步骤的活性酶。