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硫代羧化作用以及Urm1被其E1激活酶Uba4释放的分子基础。

Molecular basis for thiocarboxylation and release of Urm1 by its E1-activating enzyme Uba4.

作者信息

Sokołowski Mikołaj, Kwasna Dominika, Ravichandran Keerthiraju E, Eggers Cristian, Krutyhołowa Rościsław, Kaczmarczyk Magdalena, Skupien-Rabian Bozena, Jaciuk Marcin, Walczak Marta, Dahate Priyanka, Pabis Marta, Jemioła-Rzemińska Małgorzata, Jankowska Urszula, Leidel Sebastian A, Glatt Sebastian

机构信息

Malopolska Centre of Biotechnology (MCB), Jagiellonian University, Gronostajowa7a, 30-387 Krakow, Poland.

Postgraduate School of Molecular Medicine, Zwirki i Wigury 61, 02-091 Warsaw, Poland.

出版信息

Nucleic Acids Res. 2024 Dec 11;52(22):13980-13995. doi: 10.1093/nar/gkae1111.

Abstract

Ubiquitin-related modifier 1 (Urm1) is a highly conserved member of the ubiquitin-like (UBL) family of proteins. Urm1 is a key component of the eukaryotic transfer RNA (tRNA) thiolation cascade, responsible for introducing sulfur at wobble uridine (U34) in several eukaryotic tRNAs. Urm1 must be thiocarboxylated (Urm1-SH) by its E1 activating enzyme UBL protein activator 4 (Uba4). Uba4 first adenylates and then thiocarboxylates the C-terminus of Urm1 using its adenyl-transferase (AD) and rhodanese (RHD) domains. However, the detailed mechanisms of Uba4, the interplay between the two domains, and the release of Urm1 remain elusive. Here, we report a cryo-EM-based structural model of the Uba4/Urm1 complex that reveals the position of its RHD domains after Urm1 binding, and by analyzing the in vitro and in vivo consequence of mutations at the interface, we show its importance for the thiocarboxylation of Urm1. Our results confirm that the formation of the Uba4-Urm1 thioester and thiocarboxylation of Urm1's C-terminus depend on conserved cysteine residues of Uba4 and that the complex avoids unwanted side-reactions of the adenylate by forming a thioester intermediate. We show how the Urm1-SH product can be released and how Urm1 interacts with upstream (Tum1) and downstream (Ncs6) components of the pathway. Our work provides a detailed mechanistic description of the reaction steps that are needed to produce Urm1-SH, which is required to thiolate tRNAs and persulfidate proteins.

摘要

泛素相关修饰因子1(Urm1)是泛素样(UBL)蛋白家族中高度保守的成员。Urm1是真核生物转移RNA(tRNA)硫醇化级联反应的关键组成部分,负责在几种真核生物tRNA的摆动尿苷(U34)处引入硫。Urm1必须由其E1激活酶UBL蛋白激活因子4(Uba4)进行硫代羧化(Urm1-SH)。Uba4首先将腺苷酸化,然后利用其腺苷转移酶(AD)和硫氰酸酶(RHD)结构域将Urm1的C末端硫代羧化。然而,Uba4的详细机制、两个结构域之间的相互作用以及Urm1的释放仍不清楚。在这里,我们报告了基于冷冻电镜的Uba4/Urm1复合物结构模型,该模型揭示了Urm1结合后其RHD结构域的位置,并且通过分析界面处突变的体外和体内后果,我们展示了其对Urm1硫代羧化的重要性。我们的结果证实,Uba4-Urm1硫酯的形成和Urm1 C末端的硫代羧化取决于Uba4保守的半胱氨酸残基,并且该复合物通过形成硫酯中间体避免了腺苷酸的不必要副反应。我们展示了Urm1-SH产物如何释放以及Urm1如何与该途径的上游(Tum1)和下游(Ncs6)组分相互作用。我们的工作提供了产生Urm1-SH所需反应步骤的详细机制描述,而Urm1-SH是tRNA硫醇化和蛋白质过硫化所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92f7/11662940/634fdaf65a54/gkae1111figgra1.jpg

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