共 35 条
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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