Genome-Wide De Novo Prediction of Cis-Regulatory Binding Sites in Mycobacterium tuberculosis H37Rv

被引:2
|
作者
Wu, Wei [1 ]
Sun, Xian [1 ]
Gao, Yun [1 ]
Jiang, Jun [1 ]
Cui, Zhenling [2 ]
Ge, Baoxue [2 ]
Wu, Hai [1 ]
Zhang, Lu [1 ]
Li, Yao [1 ]
机构
[1] Fudan Univ, Coll Life Sci, Shanghai Engn Res Ctr Ind Microorganisms, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] Tongji Univ, Sch Med, Shanghai Pulm Hosp, Shanghai Key Lab TB, Shanghai 200092, Peoples R China
来源
PLOS ONE | 2016年 / 11卷 / 02期
基金
中国国家自然科学基金; 国家科技攻关计划;
关键词
TRANSCRIPTION FACTOR; REPRESSOR; DATABASE; REGULON; NUCLEOTIDE; COMPLEXITY;
D O I
10.1371/journal.pone.0148965
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The transcription regulatory system of Mycobacterium tuberculosis (M. tb) remains incompletely understood. In this study, we have applied the eGLECLUBS algorithm to a group of related prokaryotic genomes for de novo genome-wide prediction of cis-regulatory binding sites (CRBSs) inM. tb H37Rv. The top 250 clusters from our prediction recovered 83.3% (50/60) of all known CRBSs in extracted inter-operonic sequences of this strain. We further demonstrated that the integration of our prediction results with the ChIP-Seq datasets is very effective in identifying true binding sites of TFs. Using electrophoretic mobility shift assays and real-time RT-PCR, we experimentally verified our prediction of CRBSs for Rv0081, an important transcription factor thought to be involved in regulation ofM. tb under hypoxia.
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页数:11
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