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Microarray Analysis of Gene Expression in the Kidneys of New- and Post-Onset Diabetic NOD Mice

机译:基因芯片在新发和发作后糖尿病NOD小鼠肾脏中的基因表达分析

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We profiled the expression of 5,760 clones from a kidney subtraction library in the kidneys of three groups of NOD mice: nondiabetic, new-onset, and long-term diabetic. A total of 27 genes had lower expression and 1 gene (Gpx3) had higher expression in the new-onset diabetic mice compared with nondiabetic control NOD mice (P < 0.001). Similarly, 19 of the above 27 genes and 7 additional genes had higher expression and the Gpx3 gene had lower expression in long-term diabetic mice compared with controls (P < 0.001). Interestingly, only three genes may be different between new-onset and long-term diabetic mice (P < 0.0004). These genes are from diverse functional groups, including oxidative phosphorylation, free radical neutralization, channels, pumps, lipid processing, transcription and translation machinery, protein trafficking, constitutive protein processing, and immune function. The majority of these genes fall into four signaling pathways: insulin, transforming growth factor-β, tumor necrosis factor-α, and peroxisome profiferator-activated receptor. The most significant expression change was found for the stearoyl-coenzyme A desaturase 1 (SCD1) gene (P < 10~(-7)). The lower expression levels of the SCD1 gene in both diabetic groups compared with controls were further confirmed by Northern blot analysis and immunohistochemistry.
机译:我们分析了三组NOD小鼠肾脏中肾脏减损文库中5,760个克隆的表达:非糖尿病,新发糖尿病和长期糖尿病。与非糖尿病对照组的NOD小鼠相比,新发病的糖尿病小鼠中共有27个基因表达较低,而1个基因(Gpx3)具有较高的表达(P <0.001)。类似地,与对照组相比,长期糖尿病小鼠中上述27个基因中的19个基因和7个其他基因具有较高的表达,而Gpx3基因具有较低的表达(P <0.001)。有趣的是,新发病和长期糖尿病小鼠之间只有三个基因可能不同(P <0.0004)。这些基因来自不同的功能组,包括氧化磷酸化,自由基中和,通道,泵,脂质加工,转录和翻译机制,蛋白质运输,组成型蛋白质加工和免疫功能。这些基因中的大多数属于四个信号传导途径:胰岛素,转化生长因子-β,肿瘤坏死因子-α和过氧化物酶体增效剂激活的受体。硬脂酰辅酶A去饱和酶1(SCD1)基因的表达变化最为明显(P <10〜(-7))。通过Northern印迹分析和免疫组织化学进一步证实了两个糖尿病组中SCD1基因的表达水平均低于对照组。

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