Kakizuka A, Sebastian B, Borgmeyer U, Hermans-Borgmeyer I, Bolado J, Hunter T, Hoekstra M F, Evans R M
Gene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037.
Genes Dev. 1992 Apr;6(4):578-90. doi: 10.1101/gad.6.4.578.
The timing and activation of the p34cdc2 kinase in mammals is associated with dephosphorylation of phosphotyrosine and phosphothreonine residues on the p34cdc2 kinase. For fission yeast, the timing of mitosis is regulated by cyclic accumulation of cdc25, which promotes dephosphorylation of p34cdc2 and concomitant protein kinase activation. We report the identification and characterization of a structural and functional mouse homolog, Cdc25M2, of the cdc25 phosphatase. Cdc25M2 shows high sequence identity to the previously reported human homolog cdc25Hu2. Cdc25M2 can functionally complement for a Schizosaccharomyces pombe cdc25ts mutation, and when expressed in Escherichia coli and purified, Cdc25M2 is an active phosphatase. cdc25M2 mRNA shows variation in expression in different tissues in the mouse embryo and is expressed in a developmental and cell-cycle-dependent fashion. We suggest that the expression and accumulation of the cdc25 mitotic inducer may play a critical role in the regulation of mouse development.
哺乳动物中p34cdc2激酶的激活时间与该激酶上磷酸酪氨酸和磷酸苏氨酸残基的去磷酸化有关。对于裂殖酵母,有丝分裂的时间由cdc25的周期性积累调节,cdc25促进p34cdc2的去磷酸化并伴随蛋白激酶激活。我们报告了cdc25磷酸酶的一种结构和功能上的小鼠同源物Cdc25M2的鉴定和特性。Cdc25M2与先前报道的人类同源物cdc25Hu2具有高度的序列同一性。Cdc25M2能够在功能上弥补粟酒裂殖酵母cdc25ts突变,并且当在大肠杆菌中表达并纯化时,Cdc25M2是一种活性磷酸酶。cdc25M2 mRNA在小鼠胚胎的不同组织中表达存在差异,并以发育和细胞周期依赖性方式表达。我们认为cdc25有丝分裂诱导剂的表达和积累可能在小鼠发育的调节中起关键作用。