Open AccessNucleotide substitutions in CD 101 , the human homolog of a diabetes susceptibility gene in non‐obese diabetic mouse, in patients with type 1 diabetes
Author(s) -
Okuno Misako,
Kasahara Yoshihito,
Onodera Masafumi,
Takubo Noriyuki,
Okajima Michiko,
Suga Shigeru,
Watanabe Nobuyuki,
Suzuki Junichi,
Ayabe Tadayuki,
Urakami Tatsuhiko,
Kawamura Tomoyuki,
Kikuchi Nobuyuki,
Yokota Ichiro,
Kikuchi Toru,
Amemiya Shin,
Nakabayashi Kazuhiko,
Hayashi Keiko,
Hata Kenichiro,
Matsubara Yoichi,
Ogata Tsutomu,
Fukami Maki,
Sugihara Shigetaka
Publication year - 2017
Publication title -
journal of diabetes investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.089
H-Index - 50
eISSN - 2040-1124
pISSN - 2040-1116
DOI - 10.1111/jdi.12586
Subject(s) - medicine , diabetes mellitus , type 2 diabetes , gene , type 1 diabetes , single nucleotide polymorphism , nucleotide , genetics , endocrinology , bioinformatics , genotype , biology
Aims/Introduction Although genome‐wide association studies have identified more than 50 susceptibility genes for type 1 diabetes, low‐frequency risk variants could remain unrecognized. The present study aimed to identify novel type 1 diabetes susceptibility genes by newly established methods. Materials and Methods We carried out whole‐exome sequencing and genome‐wide copy‐number analysis for a Japanese family consisting of two patients with type 1 diabetes and three unaffected relatives. Further mutation screening was carried out for 127 sporadic cases. The functional consequences of identified substitutions were evaluated by in silico analyses and fluorescence‐activated cell sorting of blood samples. Results Whole‐exome sequencing and genome‐wide copy‐number analysis of familial cases showed co‐segregation of the p.V863L substitution in CD 101 , the human homolog of an autoimmune diabetes gene in the non‐obese diabetic mouse, with type 1 diabetes. Mutation screening of CD 101 in 127 sporadic cases detected the p.V678L and p.T944R substitutions in two patients. The p.V863L, p.V678L and p.T944R substitutions were absent or extremely rare in the general population, and were assessed as ‘probably/possibly damaging’ by in silico analyses. CD 101 expression on monocytes, granulocytes and myeloid dendritic cells of mutation‐positive patients was weaker than that of control individuals. Conclusions These results raise the possibility that CD 101 is a susceptibility gene for type 1 diabetes.