Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk

被引:29
作者
Huang, Yuanhua [1 ,4 ,5 ,6 ]
Xu, Bosen [2 ]
Zhou, Xueya [7 ,8 ]
Li, Ying [1 ]
Lu, Ming [1 ]
Jiang, Rui [4 ,5 ]
Li, Tingting [1 ,3 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Sch Basic Med, Dept Biomed Informat, Beijing 100191, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Sch Basic Med, Dept Biochem & Mol Biol, Beijing 100191, Peoples R China
[3] Peking Univ, Hlth Sci Ctr, Sch Basic Med, Inst Syst Biomed, Beijing 100191, Peoples R China
[4] Tsinghua Univ, MOE, Key Lab Bioinformat, Beijing 100084, Peoples R China
[5] Tsinghua Univ, Bioinformat Div, TNLIST Dept Automat, Beijing 100084, Peoples R China
[6] European Mol Biol Lab, European Bioinformat Inst, Cambridge, England
[7] Univ Hong Kong, Li Ka Shing Fac Med, Dept Psychiat, Hong Kong, Hong Kong, Peoples R China
[8] Univ Hong Kong, Li Ka Shing Fac Med, Ctr Genom Sci, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
ARGININE METHYLATION; O-GLCNACYLATION; P53; ACTIVITY; PHOSPHORYLATION; KINASE; LYSINE; TRANSCRIPTION; ACETYLATION; DEGRADATION; INFORMATION;
D O I
10.1074/mcp.M114.037994
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Post-translational modification (PTM) 1 plays an important role in regulating the functions of proteins. PTMs of multiple residues on one protein may work together to determine a functional outcome, which is known as PTM crosstalk. Identification of PTM cross-talks is an emerging theme in proteomics and has elicited great interest, but their properties remain to be systematically characterized. To this end, we collected 193 PTM cross-talk pairs in 77 human proteins from the literature and then tested location preference and co-evolution at the residue and modification levels. We found that cross-talk events preferentially occurred among nearby PTM sites, especially in disordered protein regions, and cross-talk pairs tended to co-evolve. Given the properties of PTM cross-talk pairs, a naIve Bayes classifier integrating different features was built to predict cross-talks for pairwise combination of PTM sites. By using a 10-fold cross-validation, the integrated prediction model showed an area under the receiver operating characteristic (ROC) curve of 0.833, superior to using any individual feature alone. The prediction performance was also demonstrated to be robust to the biases in the collected PTM cross-talk pairs. The integrated approach has the potential for large-scale prioritization of PTM cross-talk candidates for functional validation and was implemented as a web server available at http://bioinfo.bjmu.edu.cn/ptm-x/.
引用
收藏
页码:761 / 770
页数:10
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共 50 条
[41]  
Swaney DL, 2013, NAT METHODS, V10, P676, DOI [10.1038/nmeth.2519, 10.1038/NMETH.2519]
[42]   Cross-talk between phosphorylation and lysine acetylation in a genome-reduced bacterium [J].
van Noort, Vera ;
Seebacher, Jan ;
Bader, Samuel ;
Mohammed, Shabaz ;
Vonkova, Ivana ;
Betts, Matthew J. ;
Kuehner, Sebastian ;
Kumar, Runjun ;
Maier, Tobias ;
O'Flaherty, Martina ;
Rybin, Vladimir ;
Schmeisky, Arne ;
Yus, Eva ;
Stuelke, Joerg ;
Serrano, Luis ;
Russell, Robert B. ;
Heck, Albert J. R. ;
Bork, Peer ;
Gavin, Anne-Claude .
MOLECULAR SYSTEMS BIOLOGY, 2012, 8
[43]   The switches. ELM Resource: A Compendium of Conditional Regulatory Interaction Interfaces [J].
Van Roey, Kim ;
Dinkel, Holger ;
Weatheritt, Robert J. ;
Gibson, Toby J. ;
Davey, Norman E. .
SCIENCE SIGNALING, 2013, 6 (269) :rs7
[44]   Histone demethylases in chromatin cross-talks [J].
Verrier, Laure ;
Vandromme, Marie ;
Trouche, Didier .
BIOLOGY OF THE CELL, 2011, 103 (08) :381-401
[45]   Purification and functional characterization of a histone H3-lysine 4-specific methyltransferase [J].
Wang, HB ;
Cao, R ;
Xia, L ;
Erdjument-Bromage, H ;
Borchers, C ;
Tempst, P ;
Zhang, Y .
MOLECULAR CELL, 2001, 8 (06) :1207-1217
[46]   Methylation of histone H4 at arginine 3 facilitating transcriptional activation by nuclear hormone receptor [J].
Wang, HB ;
Huang, ZQ ;
Xia, L ;
Feng, Q ;
Erdjument-Bromage, H ;
Strahl, BD ;
Briggs, SD ;
Allis, CD ;
Wong, JM ;
Tempst, P ;
Zhang, Y .
SCIENCE, 2001, 293 (5531) :853-857
[47]   Aurora A mediates cross-talk between N- and C-terminal post-translational modifications of p53 [J].
Warnock, Lorna Jane ;
Raines, Sally Anne ;
Milner, Jo .
CANCER BIOLOGY & THERAPY, 2011, 12 (12) :1059-1068
[48]   Arginine Methylation of FOXO Transcription Factors Inhibits Their Phosphorylation by Akt [J].
Yamagata, Kazuyuki ;
Daitoku, Hiroaki ;
Takahashi, Yuta ;
Namiki, Kana ;
Hisatake, Koji ;
Kako, Koichiro ;
Mukai, Hidehito ;
Kasuya, Yoshitoshi ;
Fukamizu, Akiyoshi .
MOLECULAR CELL, 2008, 32 (02) :221-231
[49]   Modification of p53 with O-linked N-acetylglucosamine regulates p53 activity and stability [J].
Yang, Won Ho ;
Kim, Ji Eun ;
Nam, Hyung Wook ;
Ju, Jung Won ;
Kim, Hoe Suk ;
Kim, Yu Sam ;
Cho, Jin Won .
NATURE CELL BIOLOGY, 2006, 8 (10) :1074-U53
[50]   A recurrent phospho-sumoyl switch in transcriptional repression and beyond [J].
Yang, Xiang-Jiao ;
Gregoire, Serge .
MOLECULAR CELL, 2006, 23 (06) :779-786