GWAS have identified >200 risk loci for Inflammatory Bowel Disease (IBD). The majority of disease associations are known to be driven by regulatory variants. To identify the putative causative genes that are perturbed by these variants, we generate a large transcriptome data set (nine disease-relevant cell types) and identify 23,650 cis-eQTL. We show that these are determined by ∼9720 regulatory modules, of which ∼3000 operate in multiple tissues and ∼970 on multiple genes. We identify regulatory modules that drive the disease association for 63 of the 200 risk loci, and show that these are enriched in multigenic modules. Based on these analyses, we resequence 45 of the corresponding 100 candidate genes in 6600 Crohn disease (CD) cases and 5500 controls, and show with burden tests that they include likely causative genes. Our analyses indicate that ≥10-fold larger sample sizes will be required to demonstrate the causality of individual genes using this approach.

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes / Momozawa, Y.; Dmitrieva, J.; Theatre, E.; Deffontaine, V.; Rahmouni, S.; Charloteaux, B.; Crins, F.; Docampo, E.; Elansary, M.; Gori, A. -S.; Lecut, C.; Mariman, R.; Mni, M.; Oury, C.; Altukhov, I.; Alexeev, D.; Aulchenko, Y.; Amininejad, L.; Bouma, G.; Hoentjen, F.; Lowenberg, M.; Oldenburg, B.; Pierik, M. J.; Vander Meulen-De Jong, A. E.; Van Der Woude, C. J.; Visschedijk, M. C.; Lathrop, M.; Hugot, J. -P.; Weersma, R. K.; De Vos, M.; Franchimont, D.; Vermeire, S.; Kubo, M.; Louis, E.; Georges, M.; Abraham, C.; Achkar, J. -P.; Ahmad, T.; Ananthakrishnan, A. N.; Andersen, V.; Anderson, C. A.; Andrews, J. M.; Annese, V.; Aumais, G.; Baidoo, L.; Baldassano, R. N.; Bampton, P. A.; Barclay, M.; Barrett, J. C.; Bayless, T. M.; Bethge, J.; Bitton, A.; Boucher, G.; Brand, S.; Brandt, B.; Brant, S. R.; Buning, C.; Chew, A.; Cho, J. H.; Cleynen, I.; Cohain, A.; Croft, A.; Daly, M. J.; D'Amato, M.; Danese, S.; De Jong, D.; Denapiene, G.; Denson, L. A.; Devaney, K. L.; Dewit, O.; D'Inca, R.; Dubinsky, M.; Duerr, R. H.; Edwards, C.; Ellinghaus, D.; Essers, J.; Ferguson, L. R.; Festen, E. A.; Fleshner, P.; Florin, T.; Franke, A.; Fransen, K.; Gearry, R.; Gieger, C.; Glas, J.; Goyette, P.; Green, T.; Griffiths, A. M.; Guthery, S. L.; Hakonarson, H.; Halfvarson, J.; Hanigan, K.; Haritunians, T.; Hart, A.; Hawkey, C.; Hayward, N. K.; Hedl, M.; Henderson, P.; Hu, X.; Huang, H.; Hui, K. Y.; Imielinski, M.; Ippoliti, A.; Jonaitis, L.; Jostins, L.; Karlsen, T. H.; Kennedy, N. A.; Khan, M. A.; Kiudelis, G.; Krishnaprasad, K.; Kugathasan, S.; Kupcinskas, L.; Latiano, A.; Laukens, D.; Lawrance, I. C.; Lee, J. C.; Lees, C. W.; Leja, M.; Van Limbergen, J.; Lionetti, P.; Liu, J. Z.; Mahy, G.; Mansfield, J.; Massey, D.; Mathew, C. G.; Mcgovern, D. P. B.; Milgrom, R.; Mitrovic, M.; Montgomery, G. W.; Mowat, C.; Newman, W.; Ng, A.; Ng, S. C.; Ng, S. M. E.; Nikolaus, S.; Ning, K.; Nothen, M.; Oikonomou, I.; Palmieri, O.; Parkes, M.; Phillips, A.; Ponsioen, C. Y.; Potocnik, U.; Prescott, N. J.; Proctor, D. D.; Radford-Smith, G.; Rahier, J. -F.; Raychaudhuri, S.; Regueiro, M.; Rieder, F.; Rioux, J. D.; Ripke, S.; Roberts, R.; Russell, R. K.; Sanderson, J. D.; Sans, M.; Satsangi, J.; Schadt, E. E.; Schreiber, S.; Schulte, D.; Schumm, L. P.; Scott, R.; Seielstad, M.; Sharma, Y.; Silverberg, M. S.; Simms, L. A.; Skieceviciene, J.; Spain, S. L.; Steinhart, A. H.; Stempak, J. M.; Stronati, L.; Sventoraityte, J.; Targan, S. R.; Taylor, K. M.; Ter Velde, A.; Torkvist, L.; Tremelling, M.; Van Sommeren, S.; Vasiliauskas, E.; Verspaget, H. W.; Walters, T.; Wang, K.; Wang, M. -H.; Wei, Z.; Whiteman, D.; Wijmenga, C.; Wilson, D. C.; Winkelmann, J.; Xavier, R. J.; Zhang, B.; Zhang, C. K.; Zhang, H.; Zhang, W.; Zhao, H.; Zhao, Z. Z.. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 9:1(2018), p. 2427. [10.1038/s41467-018-04365-8]

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes

Stronati L.;Zhang W.;Zhao H.;
2018

Abstract

GWAS have identified >200 risk loci for Inflammatory Bowel Disease (IBD). The majority of disease associations are known to be driven by regulatory variants. To identify the putative causative genes that are perturbed by these variants, we generate a large transcriptome data set (nine disease-relevant cell types) and identify 23,650 cis-eQTL. We show that these are determined by ∼9720 regulatory modules, of which ∼3000 operate in multiple tissues and ∼970 on multiple genes. We identify regulatory modules that drive the disease association for 63 of the 200 risk loci, and show that these are enriched in multigenic modules. Based on these analyses, we resequence 45 of the corresponding 100 candidate genes in 6600 Crohn disease (CD) cases and 5500 controls, and show with burden tests that they include likely causative genes. Our analyses indicate that ≥10-fold larger sample sizes will be required to demonstrate the causality of individual genes using this approach.
2018
Adult; Aged; Aged, 80 and over; Cohort Studies; Crohn Disease; Female; Gene Expression Profiling; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Inflammatory Bowel Diseases; Male; Middle Aged; Polymorphism, Single Nucleotide; Quantitative Trait Loci; Sequence Analysis, DNA; Multifactorial Inheritance
01 Pubblicazione su rivista::01a Articolo in rivista
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes / Momozawa, Y.; Dmitrieva, J.; Theatre, E.; Deffontaine, V.; Rahmouni, S.; Charloteaux, B.; Crins, F.; Docampo, E.; Elansary, M.; Gori, A. -S.; Lecut, C.; Mariman, R.; Mni, M.; Oury, C.; Altukhov, I.; Alexeev, D.; Aulchenko, Y.; Amininejad, L.; Bouma, G.; Hoentjen, F.; Lowenberg, M.; Oldenburg, B.; Pierik, M. J.; Vander Meulen-De Jong, A. E.; Van Der Woude, C. J.; Visschedijk, M. C.; Lathrop, M.; Hugot, J. -P.; Weersma, R. K.; De Vos, M.; Franchimont, D.; Vermeire, S.; Kubo, M.; Louis, E.; Georges, M.; Abraham, C.; Achkar, J. -P.; Ahmad, T.; Ananthakrishnan, A. N.; Andersen, V.; Anderson, C. A.; Andrews, J. M.; Annese, V.; Aumais, G.; Baidoo, L.; Baldassano, R. N.; Bampton, P. A.; Barclay, M.; Barrett, J. C.; Bayless, T. M.; Bethge, J.; Bitton, A.; Boucher, G.; Brand, S.; Brandt, B.; Brant, S. R.; Buning, C.; Chew, A.; Cho, J. H.; Cleynen, I.; Cohain, A.; Croft, A.; Daly, M. J.; D'Amato, M.; Danese, S.; De Jong, D.; Denapiene, G.; Denson, L. A.; Devaney, K. L.; Dewit, O.; D'Inca, R.; Dubinsky, M.; Duerr, R. H.; Edwards, C.; Ellinghaus, D.; Essers, J.; Ferguson, L. R.; Festen, E. A.; Fleshner, P.; Florin, T.; Franke, A.; Fransen, K.; Gearry, R.; Gieger, C.; Glas, J.; Goyette, P.; Green, T.; Griffiths, A. M.; Guthery, S. L.; Hakonarson, H.; Halfvarson, J.; Hanigan, K.; Haritunians, T.; Hart, A.; Hawkey, C.; Hayward, N. K.; Hedl, M.; Henderson, P.; Hu, X.; Huang, H.; Hui, K. Y.; Imielinski, M.; Ippoliti, A.; Jonaitis, L.; Jostins, L.; Karlsen, T. H.; Kennedy, N. A.; Khan, M. A.; Kiudelis, G.; Krishnaprasad, K.; Kugathasan, S.; Kupcinskas, L.; Latiano, A.; Laukens, D.; Lawrance, I. C.; Lee, J. C.; Lees, C. W.; Leja, M.; Van Limbergen, J.; Lionetti, P.; Liu, J. Z.; Mahy, G.; Mansfield, J.; Massey, D.; Mathew, C. G.; Mcgovern, D. P. B.; Milgrom, R.; Mitrovic, M.; Montgomery, G. W.; Mowat, C.; Newman, W.; Ng, A.; Ng, S. C.; Ng, S. M. E.; Nikolaus, S.; Ning, K.; Nothen, M.; Oikonomou, I.; Palmieri, O.; Parkes, M.; Phillips, A.; Ponsioen, C. Y.; Potocnik, U.; Prescott, N. J.; Proctor, D. D.; Radford-Smith, G.; Rahier, J. -F.; Raychaudhuri, S.; Regueiro, M.; Rieder, F.; Rioux, J. D.; Ripke, S.; Roberts, R.; Russell, R. K.; Sanderson, J. D.; Sans, M.; Satsangi, J.; Schadt, E. E.; Schreiber, S.; Schulte, D.; Schumm, L. P.; Scott, R.; Seielstad, M.; Sharma, Y.; Silverberg, M. S.; Simms, L. A.; Skieceviciene, J.; Spain, S. L.; Steinhart, A. H.; Stempak, J. M.; Stronati, L.; Sventoraityte, J.; Targan, S. R.; Taylor, K. M.; Ter Velde, A.; Torkvist, L.; Tremelling, M.; Van Sommeren, S.; Vasiliauskas, E.; Verspaget, H. W.; Walters, T.; Wang, K.; Wang, M. -H.; Wei, Z.; Whiteman, D.; Wijmenga, C.; Wilson, D. C.; Winkelmann, J.; Xavier, R. J.; Zhang, B.; Zhang, C. K.; Zhang, H.; Zhang, W.; Zhao, H.; Zhao, Z. Z.. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 9:1(2018), p. 2427. [10.1038/s41467-018-04365-8]
File allegati a questo prodotto
File Dimensione Formato  
Momozawa_IBD-risk_2018.pdf

accesso aperto

Tipologia: Documento in Post-print (versione successiva alla peer review e accettata per la pubblicazione)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 1.79 MB
Formato Adobe PDF
1.79 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1508394
Citazioni
  • ???jsp.display-item.citation.pmc??? 68
  • Scopus 126
  • ???jsp.display-item.citation.isi??? 125
social impact