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The Association of Nucleobindin 2 Gene (NUCB2) Variants with Type 2 Diabetes Mellitus Among Iranian Azeri-Turkish Population

机译:Nuclebindin 2基因(NUCB2)变异与2型糖尿病患者的糖尿病患者之间的缔合作蛋白酶

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摘要

Nesfatin-1, which is derived from the NEFA/nucleobindin 2 (NUCB2) precursor, is a satiety factor secreted by several tissues, including the hypothalamus. NUCB2 gene expression positively correlates with insulin secretory capacity, as well as with insulin and glucagon gene expression in human islets. Therefore, we hypothesized that polymorphisms in the NUCB2 gene promoter influence the susceptibility for the development of diabetes. In the current study, we investigated the association of NUCB2 polymorphisms in the promoter region and 52 UTR, exonl, and 52 part of intron 1 of NUCB2 gene with type II diabetes. A total of 200 patients with type II diabetes and 200 healthy controls subjects were enrolled in this study. The 52 part of NUCB2 variants was assessed using PCR and direct sequencing. Twelve variants, including rsl86174(c.-427A > C), rs214088 (c.-406C > G), rs4757506(c.254A > G), rs369209853 (c.- 205G > A), rs214087 (c.-166G > C), rs373592192 (c.-281G > A), rsl82903196 (c.-308G > A), rs 370538176 (c.- 426C > G), rs 190662423 (c.-612C > A), rsll5148100 (c.-653G > A), rs374389403 (c.-233T > C), and rs377756452 (c.-207G > A), were identified. Analysis of the results showed that the frequency of seven of the polymorphisms [rsl86174 (c.-427A > C), rs 4757506 (c.254A > G), rs369209853 (c.-205G > A), rs214087 (c.-166G > C), and rsl82903196 (c.-308G > A)] is significantly different between patients and controls subjects (P< 0.05), which indicates the association of these polymorphisms with type 2 diabetes. Although the relationship between the promoter region of NUCB2 gene and T2D remains uncertain at present, These findings may support the role of NUCB2 gene in the regulation of the regulation of blood glucose and the increased type 2 diabetes in humans.
机译:Nesfatin-1来自Nefa / nuclebindin 2(NUCB2)前体,是由几种组织分泌的饱腹感因素,包括下丘脑。 NUCB2基因表达与胰岛素分泌能力以及人类胰岛中的胰岛素和胰高血糖素基因表达呈正相关。因此,我们假设NUCB2基因启动子中的多态性影响糖尿病发育的易感性。在目前的研究中,我们研究了NUCB2多态性在启动子区和52 UTR,EXON1和52部分NUCB2基因的52部分与II型糖尿病的第5部分的关联。本研究招生了共有200型糖尿病患者和200型健康对照受试者。使用PCR评估NUCB2变体的52部分,直接测序。 12个变体,包括RSL86174(C.-427A> C),RS214088(C.-406C> G),RS4757506(C.54A> G),RS369209853(C.-205G> A),RS214087(C.-166G> C),RS373592192(C.-281G> A),RSL82903196(C.-308G> A),Rs 370538176(C.-426C> G),RS190662423(C.-612C> A),RSLL5148100(C.-鉴定了653g> a),RS374389403(C.-233T> C)和RS377756452(C.-207G> A)。结果分析显示,七种多态性的频率[RSL86174(C.-427A> C),RS 4757506(C.54A> G),RS369209853(C.-205G> A),RS214087(C.-166G) > C)和RSL82903196(C.-308G> A)在患者和对照受试者之间有显着差异(P <0.05),这表明这些多态性与2型糖尿病的关联。虽然NUCB2基因的启动子区与T2D之间的关系仍然不确定目前,但这些发现可以支持NUCB2基因在调节血糖调节中的作用和人类中增加的2型糖尿病。

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