Wolf Arielle K, Adams-Phillips Lori C, Adams Amanda N D, Erives Albert J, Phillips Bryan T
University of Iowa, Iowa, IA, United States of America.
University of Iowa, Iowa, IA, United States of America.
Cells Dev. 2025 Jun;182:204013. doi: 10.1016/j.cdev.2025.204013. Epub 2025 Feb 25.
β-catenin is a highly conserved multifunctional protein capable of mediating cell adhesion via E-cadherin and transactivation of target genes of the canonical Wnt signaling pathway. The nematode, C. elegans contains four paralogs of β-catenin which are highly specific in their functions. Though similar in overall structure, the four beta-catenins are functionally distinct, each regulating different aspects of development. Of the four, SYS-1 is a key player in Wnt dependent asymmetric cell division (ACD). In ACD, a polarized mother will give rise to a daughter with high nuclear SYS-1 and another with low nuclear SYS-1. Despite sequence dissimilarity, SYS-1 shares a close structural resemblance with human β-catenin where it retains an unstructured amino-terminus (NTD) and 12 armadillo repeats. Using existing genome sequence data from several nematode species, we find that the four β-catenin paralogs result from 3 sequential gene duplications and neofunctionalizations during nematode evolution. SYS-1, however, lacks an unstructured carboxyl-terminus (CTD) that is essential for human β-catenin transactivation processes. This work supports the hypothesis that SYS-1 compensated for the lack of CTD by acquiring novel transactivation domains with cryptic nuclear localization signals in the NTD and the first four armadillo repeats, as shown by transactivation assays in worms and yeast. Furthermore, SYS-1 regulatory domains are not localized to the NTD as in canonical β-catenin and instead spans the entire length of the protein. Truncating SYS-1 abolishes the classical SYS-1 nuclear asymmetry, resulting in daughter cells with symmetrical SYS-1 truncation localization. A screen for SYS-1 physical interactors followed by in vivo SYS-1 localization analyses and effects on cell fate suggest that proper SYS-1 nuclear export is facilitated by XPO-1, while an interaction with IMB-3, an importin β-like protein, suggests import mechanisms. Interestingly, XPO-1 is especially required for lowering SYS-1 in the Wnt-unsignaled nucleus, suggesting a distinct mechanism for regulating asymmetric nuclear SYS-1. In summary, we provide insights on the mechanism of β-catenin evolution within nematodes and inform SYS-1 transactivation and nuclear transport mechanisms.
β-连环蛋白是一种高度保守的多功能蛋白,能够通过E-钙黏蛋白介导细胞黏附,并激活经典Wnt信号通路的靶基因。线虫秀丽隐杆线虫含有四种β-连环蛋白旁系同源物,它们的功能具有高度特异性。尽管四种β-连环蛋白的整体结构相似,但功能却截然不同,各自调节发育的不同方面。其中,SYS-1是Wnt依赖性不对称细胞分裂(ACD)中的关键因子。在ACD过程中,极化的母细胞会产生一个核内SYS-1含量高的子细胞和另一个核内SYS-1含量低的子细胞。尽管序列不同,但SYS-1与人类β-连环蛋白在结构上有密切的相似性,它保留了一个无结构的氨基末端(NTD)和12个犰狳重复序列。利用几种线虫物种现有的基因组序列数据,我们发现四种β-连环蛋白旁系同源物是线虫进化过程中3次连续的基因复制和新功能化的结果。然而,SYS-1缺乏人类β-连环蛋白激活过程所必需的无结构羧基末端(CTD)。这项研究支持了这样一种假说,即SYS-1通过在NTD和前四个犰狳重复序列中获得带有隐秘核定位信号的新型激活结构域来弥补CTD的缺失,线虫和酵母中的激活分析表明了这一点。此外,SYS-1的调节结构域不像经典β-连环蛋白那样定位于NTD,而是跨越整个蛋白质长度。截断SYS-1会消除经典的SYS-1核不对称性,导致子细胞具有对称的SYS-1截断定位。对SYS-1物理相互作用蛋白的筛选,随后进行体内SYS-1定位分析及其对细胞命运的影响,表明XPO-1促进了SYS-1的正常核输出,而与一种输入蛋白β样蛋白IMB-3的相互作用则提示了输入机制。有趣的是,在Wnt未信号化的细胞核中降低SYS-1水平特别需要XPO-1,这表明存在一种调节不对称核SYS-1的独特机制。总之,我们对线虫体内β-连环蛋白的进化机制提供了见解,并阐明了SYS-1的激活和核转运机制。