Exploration of gene-gene interaction effects using entropy-based methods

被引:71
作者
Dong, Changzheng [1 ,2 ,3 ]
Chu, Xun [2 ]
Wang, Ying [2 ]
Wang, Yi [4 ]
Jin, Li [4 ]
Shi, Tieliu [1 ]
Huang, Wei [2 ,6 ]
Li, Yixue [1 ,5 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Syst Biol, Bioinformat Ctr, Shanghai, Peoples R China
[2] Chinese Natl Human Genome Ctr Shanghai, Shanghai, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
[4] Fudan Univ, Ctr Evolut Biol, MOE Key Lab Contemporary Anthropol, Shanghai 200433, Peoples R China
[5] Shanghai Ctr Bioinformat Technol, Shanghai, Peoples R China
[6] Shanghai Jiao Tong Univ, Rui Jin Hosp, Sch Med, Shanghai 200025, Peoples R China
关键词
genetic interaction; epistasis; interaction model; entropy; logistic regression;
D O I
10.1038/sj.ejhg.5201921
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene-gene interaction may play important roles in complex disease studies, in which interaction effects coupled with single-gene effects are active. Many interaction models have been proposed since the beginning of the last century. However, the existing approaches including statistical and data mining methods rarely consider genetic interaction models, which make the interaction results lack biological or genetic meaning. In this study, we developed an entropy-based method integrating two-locus genetic models to explore such interaction effects. We performed our method to simulated and real data for evaluation. Simulation results show that this method is effective to detect gene-gene interaction and, furthermore, it is able to identify the best-fit model from various interaction models. Moreover, our method, when applied to malaria data, successfully revealed negative epistatic effect between sickle cell anemia and alpha(+)-thalassemia against malaria.
引用
收藏
页码:229 / 235
页数:7
相关论文
共 38 条
[1]   A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization [J].
Arking, Dan E. ;
Pfeufer, Arne ;
Post, Wendy ;
Kao, W. H. Linda ;
Newton-Cheh, Christopher ;
Ikeda, Morna ;
West, Kristen ;
Kashuk, Carl ;
Akyol, Mahmut ;
Perz, Siegfried ;
Jalilzadeh, Shapour ;
Illig, Thomas ;
Gieger, Christian ;
Guo, Chao-Yu ;
Larson, Martin G. ;
Wichmann, H. Erich ;
Marban, Eduardo ;
O'Donnell, Christopher J. ;
Hirschhorn, Joel N. ;
Kaeaeb, Stefan ;
Spooner, Peter M. ;
Meitinger, Thomas ;
Chakravarti, Aravinda .
NATURE GENETICS, 2006, 38 (06) :644-651
[2]  
Bateson W., 1909, Mendel's Principles of Heredity
[3]   Identifying SNPs predictive of phenotype using random forests [J].
Bureau, A ;
Dupuis, J ;
Falls, K ;
Lunetta, KL ;
Hayward, B ;
Keith, TP ;
Van Eerdewegh, P .
GENETIC EPIDEMIOLOGY, 2005, 28 (02) :171-182
[4]   Association study designs for complex diseases [J].
Cardon, LR ;
Bell, JI .
NATURE REVIEWS GENETICS, 2001, 2 (02) :91-99
[5]   Epistasis:: too often neglected in complex trait studies? [J].
Carlborg, Ö ;
Haley, CS .
NATURE REVIEWS GENETICS, 2004, 5 (08) :618-U4
[6]   A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels [J].
Chen, CH ;
Chang, CJ ;
Yang, WS ;
Chen, CL ;
Fann, CSJ .
BMC GENETICS, 2003, 4 (Suppl 1)
[7]   Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans [J].
Cordell, HJ .
HUMAN MOLECULAR GENETICS, 2002, 11 (20) :2463-2468
[8]   A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data:: Application to HLA in type 1 diabetes [J].
Cordell, HJ ;
Clayton, DG .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (01) :124-141
[9]   Detecting epistatic interactions contributing to quantitative traits [J].
Culverhouse, R ;
Klein, T ;
Shannon, W .
GENETIC EPIDEMIOLOGY, 2004, 27 (02) :141-152
[10]   A perspective on epistasis: Limits of models displaying no main effect [J].
Culverhouse, R ;
Suarez, BK ;
Lin, J ;
Reich, T .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (02) :461-471