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秀丽隐杆线虫不对称细胞分裂过程中两个Dishevelled旁系同源物独特且冗余的β-连环蛋白调节作用。

Unique and redundant β-catenin regulatory roles of two Dishevelled paralogs during C. elegans asymmetric cell division.

作者信息

Baldwin Austin T, Clemons Amy M, Phillips Bryan T

机构信息

Department of Biology, University of Iowa, 143 Biology Building, Iowa City, IA 52242-1324, USA.

Department of Biology, University of Iowa, 143 Biology Building, Iowa City, IA 52242-1324, USA

出版信息

J Cell Sci. 2016 Mar 1;129(5):983-93. doi: 10.1242/jcs.175802. Epub 2016 Jan 21.

Abstract

The Wnt/β-catenin signaling pathway is utilized across metazoans. However, the mechanism of signal transduction, especially dissociation of the β-catenin destruction complex by Dishevelled proteins, remains controversial. Here, we describe the function of the Dishevelled paralogs DSH-2 and MIG-5 in the Wnt/β-catenin asymmetry (WβA) pathway in Caenorhabditis elegans, where WβA drives asymmetric cell divisions throughout development. We find that DSH-2 and MIG-5 redundantly regulate cell fate in hypodermal seam cells. Similarly, both DSH-2 and MIG-5 are required for positive regulation of SYS-1 (a C. elegans β-catenin), but MIG-5 has a stronger effect on the polarity of SYS-1 localization. We show that MIG-5 controls cortical APR-1 (the C. elegans APC) localization. DSH-2 and MIG-5 both regulate the localization of WRM-1 (another C. elegans β-catenin), acting together as negative regulators of WRM-1 nuclear localization. Finally, we demonstrate that overexpression of DSH-2 or MIG-5 in seam cells leads to stabilization of SYS-1 in the anterior seam daughter, solidifying the Dishevelled proteins as positive regulators of SYS-1. Overall, we have further defined the role of Dishevelled in the WβA signaling pathway, and demonstrated that DSH-2 and MIG-5 regulate cell fate, β-catenin nuclear levels and the polarity of β-catenin regulation.

摘要

Wnt/β-连环蛋白信号通路在多细胞动物中广泛存在。然而,信号转导机制,尤其是由散乱蛋白介导的β-连环蛋白破坏复合物的解离,仍存在争议。在此,我们描述了秀丽隐杆线虫中散乱蛋白旁系同源物DSH-2和MIG-5在Wnt/β-连环蛋白不对称(WβA)信号通路中的功能,在该通路中,WβA在整个发育过程中驱动不对称细胞分裂。我们发现DSH-2和MIG-5在皮下缝细胞中冗余调节细胞命运。同样,DSH-2和MIG-5都是SYS-1(一种秀丽隐杆线虫β-连环蛋白)正向调节所必需的,但MIG-5对SYS-1定位的极性影响更强。我们表明MIG-5控制皮层APR-1(秀丽隐杆线虫APC)的定位。DSH-2和MIG-5都调节WRM-1(另一种秀丽隐杆线虫β-连环蛋白)的定位,共同作为WRM-1核定位的负调节因子。最后,我们证明在缝细胞中过表达DSH-2或MIG-5会导致前缝子代细胞中SYS-1的稳定,巩固了散乱蛋白作为SYS-1正向调节因子的地位。总体而言,我们进一步明确了散乱蛋白在WβA信号通路中的作用,并证明DSH-2和MIG-5调节细胞命运、β-连环蛋白核水平以及β-连环蛋白调节的极性。

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