共 111 条
ConsRM: collection and large-scale prediction of the evolutionarily conserved RNA methylation sites, with implications for the functional epitranscriptome
被引:40
作者:

Song, Bowen
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机构:
Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

Chen, Kunqi
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机构:
Fujian Med Univ, Sch Basic Med Sci, Key Lab Minist Educ Gastrointestinal Canc, Fuzhou, Peoples R China Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

Tang, Yujiao
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机构:
Univ Liverpool, Liverpool, Merseyside, England Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

Wei, Zhen
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h-index: 0
机构:
Xian Jiaotong Liverpool Univ, Dept Biol Sci, Suzhou 215123, Jiangsu, Peoples R China Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

Su, Jionglong
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h-index: 0
机构:
Xian Jiaotong Liverpool Univ, Dept Math Sci, Suzhou, Peoples R China Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

de Magalhaes, Joao Pedro
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h-index: 0
机构:
Univ Liverpool, Inst Ageing & Chron Dis, Liverpool, Merseyside, England Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

Rigden, Daniel J.
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h-index: 0
机构:
Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England

Meng, Jia
论文数: 0 引用数: 0
h-index: 0
机构:
Xian Jiaotong Liverpool Univ, Dept Biol Sci, Suzhou 215123, Jiangsu, Peoples R China Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England
机构:
[1] Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool L7 8TX, Merseyside, England
[2] Fujian Med Univ, Sch Basic Med Sci, Key Lab Minist Educ Gastrointestinal Canc, Fuzhou, Peoples R China
[3] Univ Liverpool, Liverpool, Merseyside, England
[4] Xian Jiaotong Liverpool Univ, Dept Biol Sci, Suzhou 215123, Jiangsu, Peoples R China
[5] Xian Jiaotong Liverpool Univ, Dept Math Sci, Suzhou, Peoples R China
[6] Univ Liverpool, Inst Ageing & Chron Dis, Liverpool, Merseyside, England
基金:
中国国家自然科学基金;
关键词:
conservation analysis;
N6-methyladenosine (m(6)A);
genome analysis;
scoring framework;
MESSENGER-RNA;
M(6)A METHYLATION;
NUCLEAR-RNA;
GENE-EXPRESSION;
N-6-METHYLADENOSINE;
IDENTIFICATION;
DEMETHYLASE;
N6-METHYLADENOSINE;
DATABASE;
RESIDUES;
D O I:
10.1093/bib/bbab088
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Motivation N6-methyladenosine (m(6)A) is the most prevalent RNA modification on mRNAs and lncRNAs. Evidence increasingly demonstrates its crucial importance in essential molecular mechanisms and various diseases. With recent advances in sequencing techniques, tens of thousands of m(6)A sites are identified in a typical high-throughput experiment, posing a key challenge to distinguish the functional m(6)A sites from the remaining 'passenger' (or 'silent') sites. Results: We performed a comparative conservation analysis of the human and mouse m(6)A epitranscriptomes at single site resolution. A novel scoring framework, ConsRM, was devised to quantitatively measure the degree of conservation of individual m(6)A sites. ConsRM integrates multiple information sources and a positive-unlabeled learning framework, which integrated genomic and sequence features to trace subtle hints of epitranscriptome layer conservation. With a series validation experiments in mouse, fly and zebrafish, we showed that ConsRM outperformed well-adopted conservation scores (phastCons and phyloP) in distinguishing the conserved and unconserved m(6)A sites. Additionally, the m(6)A sites with a higher ConsRM score are more likely to be functionally important. An online database was developed containing the conservation metrics of 177 998 distinct human m(6)A sites to support conservation analysis and functional prioritization of individual m(6)A sites. And it is freely accessible at: https://www.xjtlu.edu.cn/biologicalsciences/con.
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页数:17
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