TY - JOUR
T1 - Lack of association between tyrosine kinase 2 (TYK2) gene polymorphisms and susceptibility to SLE in a Japanese population
AU - Kyogoku, Chieko
AU - Morinobu, Akio
AU - Nishimura, Kunihiro
AU - Sugiyama, Daisuke
AU - Hashimoto, Hiroshi
AU - Tokano, Yoshiaki
AU - Mimori, Tsuneyo
AU - Terao, Chikashi
AU - Matsuda, Fumihiko
AU - Kuno, Takayoshi
AU - Kumagai, Shunichi
PY - 2009
Y1 - 2009
N2 - Tyrosine kinase 2 (TYK2) is a type I interferon (IFN) signaling pathway gene and was previously reported to be a risk factor for systemic lupus erythematosus (SLE) in Caucasian populations. In order to test for its genetic association with SLE in a Japanese population, TYK2 single nucleotide polymorphisms (SNPs), rs2304256, rs12720270 and rs280519, were genotyped. A case - control association study was performed in a total of 411 Japanese SLE patients and 467 healthy controls. Linkage disequilibrium (LD) among TYK2 SNPs was examined. According to the data from 94 healthy controls, non-synonymous rs2304256 resulting in Val → Phe substitution was revealed to be in a LD with rs12720270 and rs280519. Therefore, we further genotyped rs2304256 as a tag SNP in the full sample sets. As a result, no differences in genotype distribution and allelic frequencies of rs2304256 were found between SLE patients and healthy controls. In conclusion, TYK2 is not a genetic risk factor for SLE in a Japanese population. Our result suggests that there is an ethnic difference in the susceptibility genes for SLE.
AB - Tyrosine kinase 2 (TYK2) is a type I interferon (IFN) signaling pathway gene and was previously reported to be a risk factor for systemic lupus erythematosus (SLE) in Caucasian populations. In order to test for its genetic association with SLE in a Japanese population, TYK2 single nucleotide polymorphisms (SNPs), rs2304256, rs12720270 and rs280519, were genotyped. A case - control association study was performed in a total of 411 Japanese SLE patients and 467 healthy controls. Linkage disequilibrium (LD) among TYK2 SNPs was examined. According to the data from 94 healthy controls, non-synonymous rs2304256 resulting in Val → Phe substitution was revealed to be in a LD with rs12720270 and rs280519. Therefore, we further genotyped rs2304256 as a tag SNP in the full sample sets. As a result, no differences in genotype distribution and allelic frequencies of rs2304256 were found between SLE patients and healthy controls. In conclusion, TYK2 is not a genetic risk factor for SLE in a Japanese population. Our result suggests that there is an ethnic difference in the susceptibility genes for SLE.
KW - Association study
KW - Single nucleotide polymorphism (SNP)
KW - Systemic lupus erythematosus (SLE)
KW - Type I interferon (IFN) signaling pathway
KW - Tyrosine kinase 2 (TYK2)
UR - https://www.scopus.com/pages/publications/68549094358
UR - https://www.scopus.com/pages/publications/68549094358#tab=citedBy
U2 - 10.1007/s10165-009-0173-1
DO - 10.1007/s10165-009-0173-1
M3 - Article
C2 - 19440814
AN - SCOPUS:68549094358
SN - 1439-7595
VL - 19
SP - 401
EP - 406
JO - Modern Rheumatology
JF - Modern Rheumatology
IS - 4
ER -