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主要组织相容性复合体中的 RNA 代谢和监测四重奏。

An RNA Metabolism and Surveillance Quartet in the Major Histocompatibility Complex.

机构信息

The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH 43205, USA.

School of Life Science, Beijing Institute of Technology, Beijing 100081, China.

出版信息

Cells. 2019 Aug 30;8(9):1008. doi: 10.3390/cells8091008.

Abstract

At the central region of the mammalian major histocompatibility complex (MHC) is a complement gene cluster that codes for constituents of complement C3 convertases (C2, factor B and C4). Complement activation drives the humoral effector functions for immune response. Sandwiched between the genes for serine proteinase factor B and anchor protein C4 are four less known but critically important genes coding for essential functions related to metabolism and surveillance of RNA during the transcriptional and translational processes of gene expression. These four genes are NELF-E (RD), SKIV2L (SKI2W), DXO (DOM3Z) and STK19 (RP1 or G11) and dubbed as NSDK. NELF-E is the subunit E of negative elongation factor responsible for promoter proximal pause of transcription. SKIV2L is the RNA helicase for cytoplasmic exosomes responsible for degradation of de-polyadenylated mRNA and viral RNA. DXO is a powerful enzyme with pyro-phosphohydrolase activity towards 5' triphosphorylated RNA, decapping and exoribonuclease activities of faulty nuclear RNA molecules. STK19 is a nuclear kinase that phosphorylates RNA-binding proteins during transcription. STK19 is also involved in DNA repair during active transcription and in nuclear signal transduction. The genetic, biochemical and functional properties for NSDK in the MHC largely stay as a secret for many immunologists. Here we briefly review the roles of (a) NELF-E on transcriptional pausing; (b) SKIV2L on turnover of deadenylated or expired RNA 3'→5' through the Ski-exosome complex, and modulation of inflammatory response initiated by retinoic acid-inducible gene 1-like receptor (RLR) sensing of viral infections; (c) DXO on quality control of RNA integrity through recognition of 5' caps and destruction of faulty adducts in 5'→3' fashion; and (d) STK19 on nuclear protein phosphorylations. There is compelling evidence that a dysregulation or a deficiency of a NSDK gene would cause a malignant, immunologic or digestive disease.

摘要

哺乳动物主要组织相容性复合体 (MHC) 的中心区域是一个补体基因簇,该基因簇编码补体 C3 转化酶的组成部分(C2、因子 B 和 C4)。补体激活驱动免疫反应的体液效应功能。在基因因子 B 和锚定蛋白 C4 之间夹着四个不太知名但至关重要的基因,这些基因编码与代谢和 RNA 监控有关的基本功能,这些功能与基因表达的转录和翻译过程有关。这四个基因是 NELF-E(RD)、SKIV2L(SKI2W)、DXO(DOM3Z)和 STK19(RP1 或 G11),并被称为 NSDK。NELF-E 是负责转录起始近端暂停的负延伸因子 E 亚基。SKIV2L 是细胞质外泌体的 RNA 解旋酶,负责降解去 poly(A) mRNA 和病毒 RNA。DXO 是一种具有焦磷酸水解酶活性的强大酶,可作用于 5'三磷酸化 RNA,具有脱帽和核 RNA 分子外切核酸酶活性。STK19 是一种核激酶,可在转录过程中磷酸化 RNA 结合蛋白。STK19 还参与活跃转录过程中的 DNA 修复和核信号转导。MHC 中 NSDK 的遗传、生化和功能特性对许多免疫学家来说仍然是一个秘密。在这里,我们简要回顾了(a)NELF-E 在转录暂停中的作用;(b)SKIV2L 在通过 Ski-exosome 复合物使去腺苷酸化或过期的 RNA 3'→5'周转,以及视黄酸诱导基因 1 样受体 (RLR) 对病毒感染的感应引发炎症反应的调节中的作用;(c)DXO 通过识别 5' 帽和以 5'→3' 方式破坏错误的加合物来实现 RNA 完整性的质量控制;以及(d)STK19 在核蛋白磷酸化中的作用。有强有力的证据表明,NSDK 基因的失调或缺乏会导致恶性、免疫或消化疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fce/6769589/f4cdaa42ceb9/cells-08-01008-g001a.jpg

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