Robertson Scott M, Lin Rueyling
Department of Molecular Biology; University of Texas Southwestern Medical Center at Dallas; Dallas, TX USA.
Worm. 2012 Jan 1;1(1):82-9. doi: 10.4161/worm.19156.
In this commentary, we discuss how our recent paper by Yang et al. contributes a new wrinkle to the already somewhat curious Wnt signaling pathway in C. elegans. We begin with a historical perspective on the Wnt pathway in the worm, followed by a summary of the key salient point from Yang et al., 2011, namely demonstration of mutually inhibitory binding of a β-catenin SYS-1 to the N-terminus and another β-catenin WRM-1 to the C-terminus of the TCF protein POP-1, and a plausible structural explanation for these differential binding specificities. The mutually inhibitory binding creates one population of POP-1 that is bound by WRM-1, phosphorylated by the NLK kinase and exported from the nucleus, and another bound by coactivator SYS-1 that remains in the nucleus. We speculate on the evolutionary history of the four β-catenins in C. elegans and suggest a possible link between multiple β-catenin gene duplications and the requirement to reduce nuclear POP-1 levels to activate Wnt target genes.
在这篇评论文章中,我们将探讨Yang等人近期发表的论文如何为秀丽隐杆线虫中本就有些奇特的Wnt信号通路增添了新的内容。我们首先从线虫中Wnt通路的历史角度展开论述,接着总结Yang等人2011年论文的关键要点,即证明β-连环蛋白SYS-1与TCF蛋白POP-1的N端相互抑制性结合,以及另一种β-连环蛋白WRM-1与POP-1的C端相互抑制性结合,并对这些不同的结合特异性给出一个合理的结构解释。这种相互抑制性结合产生了两类POP-1,一类与WRM-1结合,被NLK激酶磷酸化并从细胞核输出,另一类与共激活因子SYS-1结合并保留在细胞核内。我们推测了秀丽隐杆线虫中四种β-连环蛋白的进化历程,并提出多个β-连环蛋白基因重复与降低细胞核内POP-1水平以激活Wnt靶基因的需求之间可能存在的联系。