Uncovering the rules for protein-protein interactions from yeast genomic data

被引:16
|
作者
Wang, Jin [1 ,2 ]
Li, Chunhe [1 ,3 ]
Wang, Erkang [1 ]
Wang, Xidi [4 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] SUNY Stony Brook, Dept Chem Phys & Appl Math, Stony Brook, NY 11790 USA
[3] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[4] Citibank NA, BR-01311920 Sao Paulo, Brazil
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
FPT; frequent pattern tree search; indentifications of protein functions; predictions of protein-protein interactions; MITOCHONDRIAL RIBOSOMAL-PROTEINS; SACCHAROMYCES-CEREVISIAE; BAYESIAN NETWORKS; DATA INTEGRATION; EXPRESSION DATA; IDENTIFICATION; GENERATION; ALGORITHM; SEQUENCES; COMPLEX;
D O I
10.1073/pnas.0806427106
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
Identifying protein-protein interactions is crucial for understanding cellular functions. Genomic data provides opportunities and challenges in identifying these interactions. We uncover the rules for predicting protein-protein interactions using a frequent pattern tree (FPT) approach modified to generate a minimum set of rules (mFPT), with rule attributes constructed from the interaction features of the yeast genomic data. The mFPT prediction accuracy is benchmarked against other commonly used methods such as Bayesian networks and logistic regressions under various statistical measures. Our study indicates that mFPT outranks other methods in predicting the protein-protein interactions for the database used. We predict a new protein-protein interaction complex whose biological function is related to premRNA splicing and new protein-protein interactions within existing complexes based on the rules generated. Our method is general and can be used to discover the underlying rules for protein-protein interactions, genomic interactions, structure-function relationships, and other fields of research.
引用
收藏
页码:3752 / 3757
页数:6
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