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A-to-I 非 synonymous RNA 编辑在泛素化位点中显著富集,并与临床特征和免疫反应相关。

A-to-I nonsynonymous RNA editing was significantly enriched in the ubiquitination site and correlated with clinical features and immune response.

机构信息

Department of Obstetrics and Gynecology, Beijing Tiantan Hospital, Capital Medical University, Bejing, China.

CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.

出版信息

Sci Rep. 2022 Sep 5;12(1):15079. doi: 10.1038/s41598-022-18926-x.

Abstract

RNA editing is a post-transcriptional process that alters RNA sequence in a site-specific manner. A-to-I editing is the most abundant as well as the most well-studied type of RNA editing. About 0.5% of A-to-I editing sites were located in the coding regions. Despite of thousands of identified A-to-I nonsynonymous editing sites, the function of nonsynonymous editing was poorly studied. Here, we found that the nonsynonymous editing was significantly enriched in the ubiquitination site, compared to the synonymous editing. This enrichment was also in a modification type dependent manner, since it was not significantly enriched in other modification types. This observation was consistent with previous study that the codons for lysine (AAG and AAA) were enriched in the preferred deamination site for RNA editing. The peptides from proteomic data in CPTAC supported that mRNAs harboring edited ubiquitination sites can be translated into protein in cells. We identified the editing sites on ubiquitination site were significantly differential edited between tumor and para-tumor samples as well as among different subtypes in TCGA datasets and also correlated with clinical outcome, especially for the nonsynonymous editing sites on GSTM5, WDR1, SSR4 and PSMC4. Finally, the enrichment analysis revealed that the function of these above genes was specifically enriched in the immune response pathway. Our study shed a light on understanding the functions of nonsynonymous editing in tumorigenesis and provided nonsynonymous editing targets for potential cancer diagnosis and therapy.

摘要

RNA 编辑是一种转录后过程,以特定的方式改变 RNA 序列。A 到 I 的编辑是最丰富也是研究最多的 RNA 编辑类型。大约 0.5%的 A 到 I 编辑位点位于编码区。尽管已经鉴定出数千个 A 到 I 非同义编辑位点,但对非同义编辑的功能研究甚少。在这里,我们发现与同义编辑相比,非同义编辑在泛素化位点显著富集。这种富集也依赖于修饰类型,因为它在其他修饰类型中没有显著富集。这一观察结果与先前的研究一致,即赖氨酸(AAG 和 AAA)的密码子在 RNA 编辑的首选脱氨酶位点富集。CPTAC 的蛋白质组学数据中的肽支持携带编辑泛素化位点的 mRNA 可以在细胞中翻译成蛋白质。我们确定了 CPTAC 数据集肿瘤和肿瘤旁样本以及 TCGA 数据集中不同亚型之间的泛素化位点编辑存在显著差异,并且与临床结果相关,特别是 GSTM5、WDR1、SSR4 和 PSMC4 上的非同义编辑位点。最后,富集分析显示,这些基因的功能特别富集在免疫反应途径中。我们的研究为理解非同义编辑在肿瘤发生中的作用提供了启示,并为潜在的癌症诊断和治疗提供了非同义编辑靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec2/9445000/acd1c1facfd7/41598_2022_18926_Fig1_HTML.jpg

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