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真核生物 5-甲基胞嘧啶(m⁵C)RNA 甲基转移酶:机制、细胞功能以及与疾病的关联。

Eukaryotic 5-methylcytosine (m⁵C) RNA Methyltransferases: Mechanisms, Cellular Functions, and Links to Disease.

机构信息

Department of Molecular Biology, University Medical Center Göttingen, Humboldtallee 23, 37073 Göttingen, Germany.

Institute of Organic Chemistry, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.

出版信息

Genes (Basel). 2019 Jan 30;10(2):102. doi: 10.3390/genes10020102.

Abstract

5-methylcytosine (m⁵C) is an abundant RNA modification that's presence is reported in a wide variety of RNA species, including cytoplasmic and mitochondrial ribosomal RNAs (rRNAs) and transfer RNAs (tRNAs), as well as messenger RNAs (mRNAs), enhancer RNAs (eRNAs) and a number of non-coding RNAs. In eukaryotes, C5 methylation of RNA cytosines is catalyzed by enzymes of the NOL1/NOP2/SUN domain (NSUN) family, as well as the DNA methyltransferase homologue DNMT2. In recent years, substrate RNAs and modification target nucleotides for each of these methyltransferases have been identified, and structural and biochemical analyses have provided the first insights into how each of these enzymes achieves target specificity. Functional characterizations of these proteins and the modifications they install have revealed important roles in diverse aspects of both mitochondrial and nuclear gene expression. Importantly, this knowledge has enabled a better understanding of the molecular basis of a number of diseases caused by mutations in the genes encoding m⁵C methyltransferases or changes in the expression level of these enzymes.

摘要

5- 甲基胞嘧啶(m⁵C)是一种丰富的 RNA 修饰,存在于多种 RNA 物种中,包括细胞质和线粒体核糖体 RNA(rRNA)和转移 RNA(tRNA),以及信使 RNA(mRNA)、增强子 RNA(eRNA)和许多非编码 RNA。在真核生物中,RNA 胞嘧啶的 C5 甲基化由 NOL1/NOP2/SUN 结构域(NSUN)家族的酶以及 DNA 甲基转移酶同源物 DNMT2 催化。近年来,已经鉴定出这些甲基转移酶的每种酶的底物 RNA 和修饰靶核苷酸,并且结构和生化分析为了解这些酶如何实现靶标特异性提供了初步见解。这些蛋白质的功能特征及其所安装的修饰揭示了它们在线粒体和核基因表达的多个方面的重要作用。重要的是,这些知识使人们更好地理解了由编码 m⁵C 甲基转移酶的基因突变或这些酶的表达水平变化引起的多种疾病的分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2558/6409601/321a51186d97/genes-10-00102-g001.jpg

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