An integrative network-based approach to identify novel disease genes and pathways: a case study in the context of inflammatory bowel disease

被引:20
作者
Eguchi, Ryohei [1 ,2 ]
Karim, Mohammand Bozlul [1 ,2 ]
Hu, Pingzhao [3 ,4 ,5 ]
Sato, Tetsuo [1 ,2 ,6 ]
Ono, Naoaki [1 ,2 ]
Kanaya, Shigehiko [1 ,2 ]
Altaf-Ul-Amin, Md. [1 ,2 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Sci & Technol, Nara, Japan
[2] Nara Inst Sci & Technol, NAIST Data Sci Ctr, Nara, Japan
[3] Univ Manitoba, Dept Biochem & Med Genet, Winnipeg, MB, Canada
[4] Univ Manitoba, George & Fay Yee Ctr Healthcare Innovat, Winnipeg, MB, Canada
[5] Univ Manitoba, Dept Elect & Comp Engn, Winnipeg, MB, Canada
[6] Gunma Prefectural Coll Hlth Sci, Dept Radiol Technol, Gunma, Japan
关键词
Disease gene; Inflammatory bowel disease; Gene expression; Protein-protein interaction; FALSE DISCOVERY RATE; FACTOR RECEPTOR; SUSCEPTIBILITY LOCI; ULCERATIVE-COLITIS; PROTEIN COMPLEXES; KAPPA-B; EXPRESSION; PRIORITIZATION; REGULATOR; NUMBER;
D O I
10.1186/s12859-018-2251-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: There are different and complicated associations between genes and diseases. Finding the causal associations between genes and specific diseases is still challenging. In this work we present a method to predict novel associations of genes and pathways with inflammatory bowel disease (IBD) by integrating information of differential gene expression, protein-protein interaction and known disease genes related to IBD. Results: We downloaded IBD gene expression data from NCBI's Gene Expression Omnibus, performed statistical analysis to determine differentially expressed genes, collected known IBD genes from DisGeNet database, which were used to construct a IBD related PPI network with HIPPIE database. We adapted our graph-based clustering algorithm DPCIusO to cluster the disease PPI network. We evaluated the statistical significance of the identified clusters in the context of determining the richness of IBD genes using Fisher's exact test and predicted novel genes related to IBD. We showed 93.8% of our predictions are correct in the context of other databases and published literatures related to IBD. Conclusions: Finding disease-causing genes is necessary for developing drugs with synergistic effect targeting many genes simultaneously. Here we present an approach to identify novel disease genes and pathways and discuss our approach in the context of IBD. The approach can be generalized to find disease-associated genes for other diseases.
引用
收藏
页数:12
相关论文
共 87 条
[1]   SUSPECTS: enabling fast and effective prioritization of positional candidates [J].
Adie, EA ;
Adams, RR ;
Evans, KL ;
Porteous, DJ ;
Pickard, BS .
BIOINFORMATICS, 2006, 22 (06) :773-774
[2]   Gene prioritization through genomic data fusion [J].
Aerts, S ;
Lambrechts, D ;
Maity, S ;
Van Loo, P ;
Coessens, B ;
De Smet, F ;
Tranchevent, LC ;
De Moor, B ;
Marynen, P ;
Hassan, B ;
Carmeliet, P ;
Moreau, Y .
NATURE BIOTECHNOLOGY, 2006, 24 (05) :537-544
[3]  
Altaf-Ul-Amin M., 2012, ISRN Biomath, V2012, DOI [10.5402/2012/726429, DOI 10.5402/2012/726429]
[4]  
Altaf-Ul-Amin M, 2006, J COMPUT AIDED CHEM, V7, P150
[5]   Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47 [J].
Anderson, Carl A. ;
Boucher, Gabrielle ;
Lees, Charlie W. ;
Franke, Andre ;
D'Amato, Mauro ;
Taylor, Kent D. ;
Lee, James C. ;
Goyette, Philippe ;
Imielinski, Marcin ;
Latiano, Anna ;
Lagace, Caroline ;
Scott, Regan ;
Amininejad, Leila ;
Bumpstead, Suzannah ;
Baidoo, Leonard ;
Baldassano, Robert N. ;
Barclay, Murray ;
Bayless, Theodore M. ;
Brand, Stephan ;
Buening, Carsten ;
Colombel, Jean-Frederic ;
Denson, Lee A. ;
De Vos, Martine ;
Dubinsky, Marla ;
Edwards, Cathryn ;
Ellinghaus, David ;
Fehrmann, Rudolf S. N. ;
Floyd, James A. B. ;
Florin, Timothy ;
Franchimont, Denis ;
Franke, Lude ;
Georges, Michel ;
Glas, Juergen ;
Glazer, Nicole L. ;
Guthery, Stephen L. ;
Haritunians, Talin ;
Hayward, Nicholas K. ;
Hugot, Jean-Pierre ;
Jobin, Gilles ;
Laukens, Debby ;
Lawrance, Ian ;
Lemann, Marc ;
Levine, Arie ;
Libioulle, Cecile ;
Louis, Edouard ;
McGovern, Dermot P. ;
Milla, Monica ;
Montgomery, Grant W. ;
Morley, Katherine I. ;
Mowat, Craig .
NATURE GENETICS, 2011, 43 (03) :246-U94
[6]   Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway [J].
Andreoletti, Gaia ;
Shakhnovich, Valentina ;
Christenson, Kathy ;
Coelho, Tracy ;
Haggarty, Rachel ;
Afzal, Nadeem A. ;
Batra, Akshay ;
Petersen, Britt-Sabina ;
Mort, Matthew ;
Beattie, R. Mark ;
Ennis, Sarah .
SCIENTIFIC REPORTS, 2017, 7
[7]  
[Anonymous], 2006, 23 INT C MACH LEARN, DOI [10.1145/1143844.1143874, DOI 10.1145/1143844.1143874]
[8]  
[Anonymous], GENOME BIOL
[9]   Tumor necrosis factor receptor-associated factors (TRAFs) - a family of adaptor proteins that regulates life and death [J].
Arch, RH ;
Gedrich, RW ;
Thompson, CB .
GENES & DEVELOPMENT, 1998, 12 (18) :2821-2830
[10]   Monitoring of blood vessels and tissues by a population of monocytes with patrolling behavior [J].
Auffray, Cedric ;
Fogg, Darin ;
Garfa, Meriem ;
Elain, Gaelle ;
Join-Lambert, Olivier ;
Kayal, Samer ;
Sarnacki, Sabine ;
Cumano, Ana ;
Lauvau, Gregoire ;
Geissmann, Frederic .
SCIENCE, 2007, 317 (5838) :666-670