Hammarsten O, Chu G
Department of Medicine, Stanford University Medical Center, CA 94305-5115, USA.
Proc Natl Acad Sci U S A. 1998 Jan 20;95(2):525-30. doi: 10.1073/pnas.95.2.525.
In mammalian cells, double-strand break repair and V(D)J recombination require DNA-dependent protein kinase (DNA-PK), a serine/threonine kinase that is activated by DNA. DNA-PK consists of a 460-kDa subunit (p460) that contains a putative kinase domain and a heterodimeric subunit (Ku) that binds to double-stranded DNA ends. Previous reports suggested that the activation of DNA-PK requires the binding of Ku to DNA. To investigate this further, p460 and Ku were purified separately to homogeneity. Surprisingly, p460 was capable of binding to DNA in the absence of Ku. The binding of p460 to double-stranded DNA ends was salt-labile and could be disrupted by single-stranded or supercoiled DNA, properties distinct from the binding of Ku to DNA. Under low salt conditions, which permitted the binding of p460 to DNA ends, the kinase was activated. Under higher salt conditions, which inhibited the binding of p460, activation of the kinase required the addition of Ku. Significantly, when the length of DNA decreased to 22 bp, Ku competed with p460 for DNA binding and inhibited kinase activity. These data demonstrate that p460 is a self-contained kinase that is activated by direct interaction with double-stranded DNA and that the role of Ku is to stabilize the binding of p460 to DNA ends.
在哺乳动物细胞中,双链断裂修复和V(D)J重组需要DNA依赖性蛋白激酶(DNA-PK),这是一种由DNA激活的丝氨酸/苏氨酸激酶。DNA-PK由一个含有假定激酶结构域的460 kDa亚基(p460)和一个与双链DNA末端结合的异源二聚体亚基(Ku)组成。先前的报道表明,DNA-PK的激活需要Ku与DNA结合。为了进一步研究这一点,分别将p460和Ku纯化至同质状态。令人惊讶的是,在没有Ku的情况下,p460能够与DNA结合。p460与双链DNA末端的结合对盐敏感,并且可以被单链或超螺旋DNA破坏,这些特性与Ku与DNA的结合不同。在低盐条件下,允许p460与DNA末端结合,激酶被激活。在较高盐条件下,抑制了p460的结合,激酶的激活需要添加Ku。值得注意的是,当DNA长度减少到22 bp时,Ku与p460竞争DNA结合并抑制激酶活性。这些数据表明,p460是一种独立的激酶,通过与双链DNA的直接相互作用而被激活,并且Ku的作用是稳定p460与DNA末端的结合。