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肥胖/糖尿病患者中人类OB基因无突变。

Absence of mutations in the human OB gene in obese/diabetic subjects.

作者信息

Maffei M, Stoffel M, Barone M, Moon B, Dammerman M, Ravussin E, Bogardus C, Ludwig D S, Flier J S, Talley M

机构信息

Department of Genetics, Rockefeller University, New York 10021, USA.

出版信息

Diabetes. 1996 May;45(5):679-82. doi: 10.2337/diab.45.5.679.

Abstract

The product of the obese (ob) gene, leptin, is a secreted protein that is important in the regulation of body weight. Mice with mutations in the ob gene are obese and diabetic and manifest reduced physical as well as metabolic activity. In this study, we tested the possibility that mutations in the OB gene may contribute to human obesity. We report the isolation and partial sequence of the human OB gene and the screening of 105 obese patients for mutations in the protein coding sequence using the technique of single-strand conformational polymorphism. No coding sequence polymorphism was found, suggesting that mutations in the coding sequence of the OB gene do not constitute a common cause of increased body weight in humans. We also identified a highly polymorphic simple dinucleotide repeat DNA polymorphism in this gene that will be useful for genetic studies.

摘要

肥胖(ob)基因的产物瘦素是一种分泌蛋白,在体重调节中起重要作用。ob基因发生突变的小鼠会出现肥胖和糖尿病症状,身体活动及代谢活动均减弱。在本研究中,我们测试了OB基因的突变可能导致人类肥胖的可能性。我们报告了人类OB基因的分离及部分序列,并用单链构象多态性技术对105名肥胖患者的蛋白质编码序列进行了突变筛查。未发现编码序列多态性,这表明OB基因编码序列的突变并非人类体重增加的常见原因。我们还在该基因中鉴定出一种高度多态的简单二核苷酸重复DNA多态性,这将有助于遗传学研究。

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