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……的转录组图谱

Transcriptome Landscape of .

作者信息

Li Xinfeng, Mei Han, Chen Fang, Tang Qing, Yu Zhaoqing, Cao Xiaojian, Andongma Binda T, Chou Shan-Ho, He Jin

机构信息

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, China.

Institute of Biochemistry and NCHU Agricultural Biotechnology Center, National Chung Hsing University, Taichung, Taiwan.

出版信息

Front Microbiol. 2017 Dec 18;8:2505. doi: 10.3389/fmicb.2017.02505. eCollection 2017.

Abstract

The non-pathogenic bacterium mc155 has been widely used as a model organism in mycobacterial research, yet a detailed study about its transcription landscape remains to be established. Here we report the transcriptome, expression profiles and transcriptional structures through growth-phase-dependent RNA sequencing (RNA-seq) as well as other related experiments. We found: (1) 2,139 transcriptional start sites (TSSs) in the genome-wide scale, of which eight samples were randomly selected and further verified by 5'-RACE; (2) 2,233 independent monocistronic or polycistronic mRNAs in the transcriptome within the operon/sub-operon structures which are classified into five groups; (3) 47.50% (1016/2139) genes were transcribed into leaderless mRNAs, with the TSSs of 41.3% (883/2139) mRNAs overlapping with the first base of the annotated start codon. Initial amino acids of MSMEG_4921 and MSMEG_6422 proteins were identified by Edman degradation, indicating the presence of distinctive widespread leaderless features in mc155. (4) 150 genes with potentially wrong structural annotation, of which 124 proposed genes have been corrected; (5) eight highly active promoters, with their activities further determined by β-galactosidase assays. These data integrated the transcriptional landscape to genome information of model organism mc155 and lay a solid foundation for further works in .

摘要

非致病性细菌mc155已被广泛用作分枝杆菌研究中的模式生物,但关于其转录图谱的详细研究仍有待开展。在此,我们通过生长阶段依赖性RNA测序(RNA-seq)以及其他相关实验报告了转录组、表达谱和转录结构。我们发现:(1)在全基因组范围内有2139个转录起始位点(TSS),其中随机选择了8个样本并通过5'-RACE进一步验证;(2)转录组中在操纵子/亚操纵子结构内有2233个独立的单顺反子或多顺反子mRNA,这些结构被分为五组;(3)47.50%(1016/2139)的基因转录为无 leader 的mRNA,41.3%(883/2139)的mRNA的TSS与注释的起始密码子的第一个碱基重叠。通过Edman降解鉴定了MSMEG_4921和MSMEG_6422蛋白的起始氨基酸,表明mc155中存在独特的广泛的无leader特征。(4)150个具有潜在错误结构注释的基因,其中124个提出的基因已得到纠正;(5)8个高活性启动子,其活性通过β-半乳糖苷酶测定进一步确定。这些数据将转录图谱与模式生物mc155的基因组信息整合在一起,为进一步的研究奠定了坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/500d/5741613/ca68db7ff57d/fmicb-08-02505-g0001.jpg

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