SUMOylation 对核糖体生物发生的调控:USP36 的新作用

Yunhan Yang, Yanping Li, Rosalie C. Sears, Xiao-Xin Sun, Mushui Dai
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摘要

核糖体生物发生对细胞生长、增殖和动物发育至关重要。它的失调会导致各种人类疾病,如核糖体病和癌症。因此,对核糖体生物发生的严格调控对正常的细胞平衡至关重要。新的证据表明,泛素化和 SUMOylation 等翻译后修饰在调控核糖体生物发生过程中起着至关重要的作用。我们最近的研究发现,USP36 是一种核极去泛素化酶(DUB),它还能作为 SUMO 连接酶调节核极蛋白基团 SUMOylation,从而对核糖体的生物发生至关重要。在此,我们概述了目前对核糖体生物发生的 SUMO 化调控的理解,并讨论了 USP36 在核极 SUMO 化中的作用。
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SUMOylation regulation of ribosome biogenesis: Emerging roles for USP36
Ribosome biogenesis is essential for cell growth, proliferation, and animal development. Its deregulation leads to various human disorders such as ribosomopathies and cancer. Thus, tight regulation of ribosome biogenesis is crucial for normal cell homeostasis. Emerging evidence suggests that posttranslational modifications such as ubiquitination and SUMOylation play a crucial role in regulating ribosome biogenesis. Our recent studies reveal that USP36, a nucleolar deubiquitinating enzyme (DUB), acts also as a SUMO ligase to regulate nucleolar protein group SUMOylation, thereby being essential for ribosome biogenesis. Here, we provide an overview of the current understanding of the SUMOylation regulation of ribosome biogenesis and discuss the role of USP36 in nucleolar SUMOylation.
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Compilation of resources on subcellular localization of lncRNA High-throughput mutational analysis of a methyltransferase ribozyme SUMOylation regulation of ribosome biogenesis: Emerging roles for USP36 Identification of regulons modulating the transcriptional response to SARS-CoV-2 infection in humans Roles of ribosomal RNA in health and disease
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