Wang S X, Dunphy W G
Division of Biology 216-76, Howard Hughes Medical Institute, California Institute of Technology, 1200 East California Blvd., Pasadena, CA 91125, USA.
FEBS Lett. 2000 Dec 29;487(2):277-81. doi: 10.1016/s0014-5793(00)02370-x.
Xenopus Chk1 (Xchk1) is required for the checkpoint-associated delay of the cell cycle in frog egg extracts containing unreplicated or UV-damaged DNA. Phosphorylation of Xchk1 at multiple sites in the SQ/TQ domain (residues 314-366) in response to unreplicated or UV-damaged DNA results in elevation of its kinase activity. We have found that mutagenesis of Thr-377 in the conserved Thr-Arg-Phe (TRF) motif of Xchk1 also leads to a substantial increase in kinase activity. Thr-377 does not appear to be a site of phosphorylation in Xchk1. These findings suggest that Thr-377 may play a role in suppressing the activity of Xchk1.
非洲爪蟾Chk1(Xchk1)对于含有未复制或紫外线损伤DNA的蛙卵提取物中细胞周期的检查点相关延迟是必需的。响应未复制或紫外线损伤的DNA,SQ/TQ结构域(第314 - 366位氨基酸残基)中多个位点的Xchk1磷酸化导致其激酶活性升高。我们发现,Xchk1保守的苏氨酸-精氨酸-苯丙氨酸(TRF)基序中的苏氨酸-377发生诱变也会导致激酶活性大幅增加。苏氨酸-377似乎不是Xchk1的磷酸化位点。这些发现表明,苏氨酸-377可能在抑制Xchk1的活性中发挥作用。