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T1TAdb:I 型毒素-抗毒素系统数据库。

T1TAdb: the database of type I toxin-antitoxin systems.

机构信息

University of Bordeaux, CNRS, INSERM, ARNA, UMR 5320, U1212, F-33000 Bordeaux, France.

出版信息

RNA. 2021 Dec;27(12):1471-1481. doi: 10.1261/rna.078802.121. Epub 2021 Sep 16.

Abstract

Type I toxin-antitoxin (T1TA) systems constitute a large class of genetic modules with antisense RNA (asRNA)-mediated regulation of gene expression. They are widespread in bacteria and consist of an mRNA coding for a toxic protein and a noncoding asRNA that acts as an antitoxin preventing the synthesis of the toxin by directly base-pairing to its cognate mRNA. The co- and post-transcriptional regulation of T1TA systems is intimately linked to RNA sequence and structure, therefore it is essential to have an accurate annotation of the mRNA and asRNA molecules to understand this regulation. However, most T1TA systems have been identified by means of bioinformatic analyses solely based on the toxin protein sequences, and there is no central repository of information on their specific RNA features. Here we present the first database dedicated to type I TA systems, named T1TAdb. It is an open-access web database (https://d-lab.arna.cnrs.fr/t1tadb) with a collection of ∼1900 loci in ∼500 bacterial strains in which a toxin-coding sequence has been previously identified. RNA molecules were annotated with a bioinformatic procedure based on key determinants of the mRNA structure and the genetic organization of the T1TA loci. Besides RNA and protein secondary structure predictions, T1TAdb also identifies promoter, ribosome-binding, and mRNA-asRNA interaction sites. It also includes tools for comparative analysis, such as sequence similarity search and computation of structural multiple alignments, which are annotated with covariation information. To our knowledge, T1TAdb represents the largest collection of features, sequences, and structural annotations on this class of genetic modules.

摘要

I 型毒素-抗毒素(T1TA)系统是一大类具有反义 RNA(asRNA)介导的基因表达调控的遗传模块。它们广泛存在于细菌中,由编码毒性蛋白的 mRNA 和作为抗毒素的非编码 asRNA 组成,后者通过与同源 mRNA 直接碱基配对来防止毒素的合成。T1TA 系统的共转录和后转录调控与 RNA 序列和结构密切相关,因此准确注释 mRNA 和 asRNA 分子对于理解这种调控至关重要。然而,大多数 T1TA 系统是通过仅基于毒素蛋白序列的生物信息学分析来识别的,并且没有关于其特定 RNA 特征的信息中央存储库。在这里,我们提出了第一个专门用于 I 型 TA 系统的数据库,命名为 T1TAdb。它是一个开放访问的网络数据库(https://d-lab.arna.cnrs.fr/t1tadb),其中包含约 1900 个位点,分布在约 500 种细菌菌株中,这些菌株之前已经鉴定出毒素编码序列。RNA 分子是通过基于 mRNA 结构关键决定因素和 T1TA 基因座遗传组织的生物信息学程序进行注释的。除了 RNA 和蛋白质二级结构预测外,T1TAdb 还可以识别启动子、核糖体结合和 mRNA-asRNA 相互作用位点。它还包括用于比较分析的工具,例如序列相似性搜索和结构多重比对的计算,这些都带有共变信息进行注释。据我们所知,T1TAdb 代表了这一类遗传模块的最大特征、序列和结构注释集合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cbe/8594479/3bedd01f90de/1471f01.jpg

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