González Rodrigo, Tirado Ares, Balanda Monserrat, Alvo Miriam, Barquín Inés, Durruty Pilar, Lobos Sergio, Seelenfreund Daniela
Laboratorio de Bioquímica, Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Santiago, Chile.
Biol Res. 2007;40(3):357-64. Epub 2008 Apr 17.
Diabetic nephropathy (DN) is one of the major complications of type 2 diabetes and is associated with coronary disease. Nephrin, a protein mainly expressed in glomeruli, is decreased in DN and other kidney diseases. Since insulin levels are misregulated in type 2 diabetes, a possible connection between DN and its decreased nephrin expression could be the presence of regulatory elements responsive to insulin in the nephrin gene (NPHS1) promoter region. In this work, using bioinformatic tools, we identified a purine-rich GAGA element in the nephrin gene promoter and conducted a genomic study in search of the presence of polymorphisms in this element and its possible association with DN in type 2 diabetic patients. We amplified and sequenced a 514 bp promoter region of 100 individuals and found no genetic variants in the purine-rich GAGA-box of the nephrin gene promoter between groups of patients with diabetes type 2 with and without renal and coronary complications, control patients without diabetes and healthy controls.
糖尿病肾病(DN)是2型糖尿病的主要并发症之一,与冠心病相关。Nephrin是一种主要在肾小球表达的蛋白质,在糖尿病肾病和其他肾脏疾病中表达降低。由于2型糖尿病患者胰岛素水平失调,糖尿病肾病与其nephrin表达降低之间的一个可能联系可能是nephrin基因(NPHS1)启动子区域存在对胰岛素有反应的调控元件。在这项研究中,我们使用生物信息学工具,在nephrin基因启动子中鉴定出一个富含嘌呤的GAGA元件,并进行了一项基因组研究,以寻找该元件中多态性的存在及其与2型糖尿病患者糖尿病肾病的可能关联。我们扩增并测序了100名个体的514 bp启动子区域,发现在伴有和不伴有肾脏及冠状动脉并发症的2型糖尿病患者组、无糖尿病的对照患者和健康对照之间,nephrin基因启动子的富含嘌呤的GAGA框中没有基因变异。