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Assembly and function of branched ubiquitin chains

泛素 泛素连接酶 细胞生物学 功能(生物学) 翻译后修饰 化学 泛素结合酶 生物 生物化学 基因
作者
SriDurgaDevi Kolla,Mengchen Ye,Kevin G. Mark,Michael Rapé
出处
期刊:Trends in Biochemical Sciences [Elsevier BV]
卷期号:47 (9): 759-771 被引量:105
标识
DOI:10.1016/j.tibs.2022.04.003
摘要

Branched ubiquitin chains are abundant in cells and produced in response to specific signals. Branched chains can be assembled by multiple mechanisms that often require collaboration between ubiquitylation enzymes. Branched ubiquitin chains are dynamic, and deubiquitylases can edit, rather than terminate, signaling by branched chains. Branched ubiquitin chains encode diverse functions that range from improving the efficiency of protein degradation to organizing large signaling complexes. Small molecule-induced protein degradation often requires branched ubiquitin chains for efficient removal of a therapeutic target. Post-translational modification with ubiquitin is required for cell division, differentiation, and survival in all eukaryotes. As part of an intricate signaling code, ubiquitin is attached to its targets as single molecules or polymeric chains, with the distinct modifications encoding a wide range of outcomes. After early work focused on homotypic ubiquitin chains, such as the K48-linked polymers that drive proteasomal degradation, recent studies noted abundant conjugates that contained ubiquitin molecules modified on two or more sites. Such branched ubiquitin chains are produced in response to specific signals and they exert functions that are critical for cellular and organismal homeostasis. In this review, we will discuss our rapidly evolving understanding of the assembly and function of branched ubiquitin chains. Post-translational modification with ubiquitin is required for cell division, differentiation, and survival in all eukaryotes. As part of an intricate signaling code, ubiquitin is attached to its targets as single molecules or polymeric chains, with the distinct modifications encoding a wide range of outcomes. After early work focused on homotypic ubiquitin chains, such as the K48-linked polymers that drive proteasomal degradation, recent studies noted abundant conjugates that contained ubiquitin molecules modified on two or more sites. Such branched ubiquitin chains are produced in response to specific signals and they exert functions that are critical for cellular and organismal homeostasis. In this review, we will discuss our rapidly evolving understanding of the assembly and function of branched ubiquitin chains.
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