Shin T H, Yasuda J, Rocheleau C E, Lin R, Soto M, Bei Y, Davis R J, Mello C C
University of Massachusetts Medical School, Program in Molecular Medicine, Worcester 01605, USA.
Mol Cell. 1999 Aug;4(2):275-80. doi: 10.1016/s1097-2765(00)80375-5.
In C. elegans, a Wnt/WG-like signaling pathway down-regulates the TCF/LEF-related protein, POP-1, to specify posterior cell fates. Effectors of this signaling pathway include a beta-catenin homolog, WRM-1, and a conserved protein kinase, LIT-1. WRM-1 and LIT-1 form a kinase complex that can directly phosphorylate POP-1, but how signaling activates WRM-1/LIT-1 kinase is not yet known. Here we show that mom-4, a genetically defined effector of polarity signaling, encodes a MAP kinase kinase kinase-related protein that stimulates the WRM-1/LIT-1-dependent phosphorylation of POP-1. LIT-1 kinase activity requires a conserved residue analogous to an activating phosphorylation site in other kinases, including MAP kinases. These findings suggest that anterior/posterior polarity signaling in C. elegans may involve a MAP kinase-like signaling mechanism.
在秀丽隐杆线虫中,一种类Wnt/WG信号通路下调TCF/LEF相关蛋白POP-1,以确定后部细胞命运。该信号通路的效应器包括β-连环蛋白同源物WRM-1和保守的蛋白激酶LIT-1。WRM-1和LIT-1形成一种激酶复合物,可直接磷酸化POP-1,但信号如何激活WRM-1/LIT-1激酶尚不清楚。在这里,我们表明,mom-4是一种遗传学定义的极性信号效应器,编码一种与丝裂原活化蛋白激酶激酶激酶相关的蛋白,该蛋白刺激POP-1的WRM-1/LIT-1依赖性磷酸化。LIT-1激酶活性需要一个保守残基,类似于其他激酶(包括丝裂原活化蛋白激酶)中的激活磷酸化位点。这些发现表明,秀丽隐杆线虫中的前后极性信号可能涉及一种类丝裂原活化蛋白激酶信号机制。