Centre for Cancer Biology, University of South Australia, GPO Box 2471, Adelaide, SA, 5001, Australia.
Cell Death Differ. 2021 Feb;28(2):455-472. doi: 10.1038/s41418-020-00707-6. Epub 2021 Jan 5.
The HECT (homologous to E6AP C-terminus) ubiquitin ligases (E3s) are a small family of highly conserved enzymes involved in diverse cellular functions and pathological conditions. Characterised by a C-terminal HECT domain that accepts ubiquitin from E2 ubiquitin conjugating enzymes, these E3s regulate key signalling pathways. The activity and functional regulation of HECT E3s are controlled by several factors including post-translational modifications, inter- and intramolecular interactions and binding of co-activators and adaptor proteins. In this review, we focus on the regulation of HECT E3s by accessory proteins or adaptors and discuss various ways by which adaptors mediate their regulatory roles to affect physiological outcomes. We discuss common features that are conserved from yeast to mammals, regardless of the type of E3s as well as shed light on recent discoveries explaining some existing enigmas in the field.
HECT(E6AP C 端同源物)泛素连接酶(E3s)是一个小的高度保守的酶家族,参与多种细胞功能和病理状况。其特征是 C 端 HECT 结构域接受 E2 泛素连接酶的泛素,这些 E3s 调节关键信号通路。HECT E3s 的活性和功能调节受多种因素控制,包括翻译后修饰、分子间和分子内相互作用以及共激活因子和衔接蛋白的结合。在这篇综述中,我们重点讨论了辅助蛋白或衔接蛋白对 HECT E3s 的调节,并讨论了衔接蛋白介导其调节作用以影响生理结果的各种方式。我们讨论了从酵母到哺乳动物都保守的共同特征,无论 E3s 的类型如何,并阐明了一些最近的发现,这些发现解释了该领域的一些现有谜团。