Shi De-Li
Developmental Biology Laboratory, CNRS-UMR 7622, IBPS, Sorbonne University, Paris, France.
Front Cell Dev Biol. 2020 Sep 30;8:588370. doi: 10.3389/fcell.2020.588370. eCollection 2020.
Dishevelled proteins are key players of Wnt signaling pathways. They transduce Wnt signals and perform cellular functions through distinct conserved domains. Due to the presence of multiple paralogs, the abundant accumulation of maternal transcripts, and the activation of distinct Wnt pathways, their regulatory roles during vertebrate early development and the mechanism by which they dictate the pathway specificity have been enigmatic and attracted much attention in the past decades. Extensive studies in different animal models have provided significant insights into the structure-function relationship of conserved Dishevelled domains in Wnt signaling and the implications of Dishevelled isoforms in early developmental processes. Notably, intra- and inter-molecular interactions and Dishevelled dosage may be important in modulating the specificity of Wnt signaling. There are also distinct and redundant functions among Dishevelled isoforms in development and disease, which may result from differential spatiotemporal expression patterns and biochemical properties and post-translational modifications. This review presents the advances and perspectives in understanding Dishevelled-mediated Wnt signaling during gastrulation and neurulation in vertebrate early embryos.
蓬乱蛋白是Wnt信号通路的关键参与者。它们转导Wnt信号,并通过不同的保守结构域执行细胞功能。由于存在多个旁系同源物、母体转录本的大量积累以及不同Wnt通路的激活,它们在脊椎动物早期发育过程中的调控作用以及决定通路特异性的机制在过去几十年中一直是个谜,并引起了广泛关注。在不同动物模型中的广泛研究为Wnt信号中保守的蓬乱结构域的结构-功能关系以及蓬乱亚型在早期发育过程中的影响提供了重要见解。值得注意的是,分子内和分子间相互作用以及蓬乱蛋白的剂量可能在调节Wnt信号的特异性方面很重要。蓬乱亚型在发育和疾病中也具有不同和冗余的功能,这可能是由于不同的时空表达模式、生化特性和翻译后修饰所致。本综述介绍了在理解脊椎动物早期胚胎原肠胚形成和神经胚形成过程中蓬乱蛋白介导的Wnt信号方面的进展和观点。