Molecular screening in Japanese and Asian Indian NIDDM patients associated with obesity

被引:59
作者
Niki, T
Mori, H
Tamori, Y
KishimotoHashiramoto, M
Ueno, H
Araki, S
Masugi, J
Sawant, N
Majithia, HR
Rais, N
Hashiramoto, M
Taniguchi, H
Kasuga, M
机构
[1] KOBE UNIV,SCH MED,DEPT INTERNAL MED 2,CHUO KU,KOBE 650,JAPAN
[2] KOBE UNIV,SCH MED,FAC HLTH SCI,KOBE 650,JAPAN
[3] SIR HURKISONDAS NURROTAMDAS MED RES SOC,BOMBAY,MAHARASHTRA,INDIA
关键词
D O I
10.2337/diabetes.45.5.675
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mouse obese (ob) gene has recently been isolated through the positional cloning technique and has been proved to result in the obese and NIDDM phenotype in mice when mutated (Nature 372:425-432, 1994). More recently, it has been demonstrated, by experiments with recombinant ob protein, that ob gene product can cause mice, including ob/ob mice, diet-induced obesity mice, and normal mice, to lower their food intake and body weight (Science 269:540-549, 1995). To investigate the genetic and/or environmental fluences underlying the development of NIDDM associated with obesity, we isolated and partially sequenced the human obese (OB) gene. The human OB gene isolated in this study encoded 167 amino acids and its open reading frame was revealed to be divided into two parts with an intermediate intron of similar to 2.4 kb. Using the single-strand conformation polymorphism (SSCP) technique, we screened Japanese and Asian Indian subjects for mutations in the protein coding regions of the OB gene. A total of 75 NIDDM patients with obesity (54 Japanese and 21 Asian Indians), 40 NIDDM patients without obesity (34 Japanese and 6 Asian Indians), and 34 Japanese patients with simple obesity showed no abnormal SSCP patterns in either component of the coding sequences. These results suggested that mutations in the coding regions of the OB gene are not Likely to be commonly identifiable and that there would likely be a kind of obesity-associated NIDDM not caused by mutations of the OB gene.
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收藏
页码:675 / 678
页数:4
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