TY - JOUR
T1 - An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn’s Disease in Japanese Populations
AU - Kakuta, Yoichi
AU - Ichikawa, Ryo
AU - Fuyuno, Yuta
AU - Hirano, Atsushi
AU - Umeno, Junji
AU - Torisu, Takehiro
AU - Watanabe, Kazuhiro
AU - Asakura, Akihiro
AU - Nakano, Takeru
AU - Izumiyama, Yasuhiro
AU - Okamoto, Daisuke
AU - Naito, Takeo
AU - Moroi, Rintaro
AU - Kuroha, Masatake
AU - Kanazawa, Yoshitake
AU - Kimura, Tomoya
AU - Shiga, Hisashi
AU - Naito, Takeshi
AU - Esaki, Motohiro
AU - Kawai, Yosuke
AU - Tokunaga, Katsushi
AU - Nakamura, Minoru
AU - Matsumoto, Takayuki
AU - Nagasaki, Masao
AU - Kinouchi, Yoshitaka
AU - Unno, Michiaki
AU - Masamune, Atsushi
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Numbers JP15H04805, 18K07929 and in part by the Tohoku Medical Megabank Project (Special Account for reconstruction from the Great East Japan Earthquake). SNP genotyping was supported in part by the Center of Innovation Program from the Japan Science and Technology Agency, JST. Computational resources were provided in part by the ToMMo supercomputer system.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Expression quantitative trait locus (eQTL) analyses have enabled us to predict the function of disease susceptibility SNPs. However, eQTL for the effector memory T cells (TEM) located in the lamina propria mononuclear cells (LPMCs), which play an important role in Crohn’s disease (CD), are not yet available. Thus, we conducted RNA sequencing and eQTL analyses of TEM cells located in the LPMCs from IBD patients (n = 20). Genome-wide association study (GWAS) was performed using genotyping data of 713 Japanese CD patients and 2,063 controls. We compared the results of GWAS and eQTL of TEM, and also performed a transcriptome-wide association study using eQTL from Genotype Tissue Expression project. By eQTL analyses of TEM, correlations of possible candidates were confirmed in 22,632 pairs and 2,463 genes. Among these candidates, 19 SNPs which showed significant correlation with tenascin-XA (TNXA) expression were significantly associated with CD in GWAS. By TWAS, TNFSF15 (FDR = 1.35e-13) in whole blood, ERV3-1 (FDR = 2.18e-2) in lymphocytes, and ZNF713 (FDR = 3.04e-2) in the sigmoid colon was significantly associated with CD. By conducting integration analyses using GWAS and eQTL data, we confirmed multiple gene transcripts are involved in the development of CD.
AB - Expression quantitative trait locus (eQTL) analyses have enabled us to predict the function of disease susceptibility SNPs. However, eQTL for the effector memory T cells (TEM) located in the lamina propria mononuclear cells (LPMCs), which play an important role in Crohn’s disease (CD), are not yet available. Thus, we conducted RNA sequencing and eQTL analyses of TEM cells located in the LPMCs from IBD patients (n = 20). Genome-wide association study (GWAS) was performed using genotyping data of 713 Japanese CD patients and 2,063 controls. We compared the results of GWAS and eQTL of TEM, and also performed a transcriptome-wide association study using eQTL from Genotype Tissue Expression project. By eQTL analyses of TEM, correlations of possible candidates were confirmed in 22,632 pairs and 2,463 genes. Among these candidates, 19 SNPs which showed significant correlation with tenascin-XA (TNXA) expression were significantly associated with CD in GWAS. By TWAS, TNFSF15 (FDR = 1.35e-13) in whole blood, ERV3-1 (FDR = 2.18e-2) in lymphocytes, and ZNF713 (FDR = 3.04e-2) in the sigmoid colon was significantly associated with CD. By conducting integration analyses using GWAS and eQTL data, we confirmed multiple gene transcripts are involved in the development of CD.
UR - http://www.scopus.com/inward/record.url?scp=85087086754&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85087086754&partnerID=8YFLogxK
U2 - 10.1038/s41598-020-66951-5
DO - 10.1038/s41598-020-66951-5
M3 - Article
C2 - 32581322
AN - SCOPUS:85087086754
SN - 2045-2322
VL - 10
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 10236
ER -