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m6A-Atlas v2.0:用于揭示多种物种中 N6-甲基腺苷(m6A)转录后修饰组图谱的更新资源。

m6A-Atlas v2.0: updated resources for unraveling the N6-methyladenosine (m6A) epitranscriptome among multiple species.

机构信息

Key Laboratory of Ministry of Education for Gastrointestinal Cancer, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian 350004, China.

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215123, China.

出版信息

Nucleic Acids Res. 2024 Jan 5;52(D1):D194-D202. doi: 10.1093/nar/gkad691.

Abstract

N 6-Methyladenosine (m6A) is one of the most abundant internal chemical modifications on eukaryote mRNA and is involved in numerous essential molecular functions and biological processes. To facilitate the study of this important post-transcriptional modification, we present here m6A-Atlas v2.0, an updated version of m6A-Atlas. It was expanded to include a total of 797 091 reliable m6A sites from 13 high-resolution technologies and two single-cell m6A profiles. Additionally, three methods (exomePeaks2, MACS2 and TRESS) were used to identify >16 million m6A enrichment peaks from 2712 MeRIP-seq experiments covering 651 conditions in 42 species. Quality control results of MeRIP-seq samples were also provided to help users to select reliable peaks. We also estimated the condition-specific quantitative m6A profiles (i.e. differential methylation) under 172 experimental conditions for 19 species. Further, to provide insights into potential functional circuitry, the m6A epitranscriptomics were annotated with various genomic features, interactions with RNA-binding proteins and microRNA, potentially linked splicing events and single nucleotide polymorphisms. The collected m6A sites and their functional annotations can be freely queried and downloaded via a user-friendly graphical interface at: http://rnamd.org/m6a.

摘要

N6-甲基腺苷(m6A)是真核生物 mRNA 上最丰富的内部化学修饰之一,参与了许多重要的分子功能和生物学过程。为了促进对这种重要的转录后修饰的研究,我们在此展示了 m6A-Atlas v2.0,这是 m6A-Atlas 的更新版本。它扩展到包括来自 13 种高分辨率技术和两种单细胞 m6A 图谱的总共 797091 个可靠的 m6A 位点。此外,还使用了三种方法(exomePeaks2、MACS2 和 TRESS)从涵盖 42 个物种 651 个条件的 2712 个 MeRIP-seq 实验中鉴定出>1600 万个 m6A 富集峰。还提供了 MeRIP-seq 样品的质量控制结果,以帮助用户选择可靠的峰。我们还为 19 个物种的 172 个实验条件下估计了条件特异性的定量 m6A 图谱(即差异甲基化)。此外,为了深入了解潜在的功能电路,将 m6A 表转录组学与各种基因组特征、与 RNA 结合蛋白和 microRNA 的相互作用、潜在的连接剪接事件和单核苷酸多态性进行了注释。收集的 m6A 位点及其功能注释可以通过用户友好的图形界面在以下网址进行免费查询和下载:http://rnamd.org/m6a。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc63/10768109/02e887aa0557/gkad691figgra1.jpg

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