Mizumoto Kota, Sawa Hitoshi
Laboratory for Cell Fate Decision, Riken, Center for Developmental Biology, Kobe 650-0047, Japan.
Trends Cell Biol. 2007 Oct;17(10):465-73. doi: 10.1016/j.tcb.2007.08.004. Epub 2007 Oct 4.
In various organisms, cells divide asymmetrically to produce distinct daughter cells. In the nematode Caenorhabditis elegans, asymmetric division is controlled by the asymmetric activity of a Wnt signaling pathway (the Wnt/beta-catenin asymmetry pathway). In this process, two specialized beta-catenin homologs have crucial roles in the transmission of Wnt signals to the asymmetric activity of a T-cell factor (TCF)-type transcription factor, POP-1, in the daughter cells. One beta-catenin homolog regulates the distinct nuclear level of POP-1, and the other functions as a coactivator of POP-1. Both beta-catenins localize asymmetrically in the daughter nuclei using different mechanisms. The recent discovery of reiterative nuclear asymmetries of a highly conserved beta-catenin in an annelid suggests that similar molecular mechanisms might regulate asymmetric cell divisions in other organisms.
在各种生物体中,细胞进行不对称分裂以产生不同的子细胞。在线虫秀丽隐杆线虫中,不对称分裂由Wnt信号通路(Wnt/β-连环蛋白不对称通路)的不对称活性控制。在此过程中,两个特殊的β-连环蛋白同源物在将Wnt信号传递至子细胞中T细胞因子(TCF)型转录因子POP-1的不对称活性方面发挥着关键作用。一个β-连环蛋白同源物调节POP-1在细胞核中的不同水平,另一个则作为POP-1的共激活因子发挥作用。两种β-连环蛋白通过不同机制在子细胞核中不对称定位。最近在一种环节动物中发现一种高度保守的β-连环蛋白存在反复的核不对称现象,这表明类似的分子机制可能调控其他生物体中的不对称细胞分裂。