Baier L J, Dobberfuhl A M, Pratley R E, Hanson R L, Bogardus C
Phoenix Epidemiology and Clinical Research Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Arizona 85016, USA.
J Clin Endocrinol Metab. 1998 Aug;83(8):2993-6. doi: 10.1210/jcem.83.8.5043.
Electrophoretic variants of the vitamin D-binding protein (DBP) have been associated with type 2 diabetes as well as with metabolic characteristics that predispose to type 2 diabetes in several populations. The Gc gene that encodes DBP maps to chromosome 4q12, a region that has recently been found to be potentially linked to plasma glucose and insulin concentrations in Pima Indians. Therefore, the gene that encodes DBP was analyzed as a candidate gene for our linkage findings in the Pima Indians. Sequence analysis of the coding exons identified two previously described missense polymorphisms at codons 416 and 420, which are the genetic basis for the three common electrophoretic variants of DBP (Gc1f, Gc1s, and Gc2). These variants in DBP were associated with differences in oral glucose tolerance in nondiabetic Pima Indians.
维生素D结合蛋白(DBP)的电泳变体与2型糖尿病以及在多个人群中易患2型糖尿病的代谢特征有关。编码DBP的Gc基因定位于4号染色体q12区域,最近发现该区域可能与皮马印第安人的血糖和胰岛素浓度有关。因此,编码DBP的基因被作为皮马印第安人连锁研究结果的候选基因进行分析。对编码外显子的序列分析确定了密码子416和420处两个先前描述的错义多态性,这是DBP三种常见电泳变体(Gc1f、Gc1s和Gc2)的遗传基础。DBP中的这些变体与非糖尿病皮马印第安人的口服葡萄糖耐量差异有关。