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鉴定一种新型大鼠肝脏基因,该基因由胰岛素早期诱导产生,与葡萄糖无关。

Identification of a novel rat hepatic gene induced early by insulin, independently of glucose.

作者信息

Coffy Sandrine, Decaux Jean-François, Girard Jean, de Keyzer Yves, Asfari Maryam

机构信息

Institut Cochin, INSERM U567, CNRS UMR8104, Département d'Endocrinologie, Université Paris 5, 24 rue du Faubourg Saint-Jacques, 75014 Paris, France.

出版信息

Biochem J. 2005 Jan 1;385(Pt 1):165-71. doi: 10.1042/BJ20040586.

Abstract

We used mRNA differential display to identify new genes induced early after exposure to insulin. Our screening strategy was based on the comparison of gene expression during the time course of insulin induction in the liver of 12-day-old suckling rats both in vivo and in vitro. A novel, early induced transcript, EIIH, was identified that encodes a 353-amino-acid protein with several features suggesting that it may be secreted or bound to membranes. EIIH is also distantly related to a variety of LRR (leucine-rich repeat) proteins. Insulin treatment increased EIIH mRNA levels in the hepatocytes of suckling, fasted adult and STZ (streptozotocin)-treated diabetic rats, where insulin was required to maintain the basal level of EIIH expression. EIIH expression was induced during the suckling/weaning transition, and remained detectable thereafter. Tissue distribution analysis in adult rats revealed a pattern of expression mainly in the liver, intestine and islets of Langerhans, closely following that of the Glut2 (glucose transporter 2), suggesting that it may play a role in carbohydrate metabolism. EIIH may be a primary target of the transcriptional regulation by insulin, and may therefore constitute a new model to study the mechanisms by which insulin acts on gene transcription.

摘要

我们利用mRNA差异显示技术来鉴定暴露于胰岛素后早期诱导产生的新基因。我们的筛选策略基于对12日龄哺乳大鼠肝脏在体内和体外胰岛素诱导过程中基因表达的时间进程进行比较。我们鉴定出一种新的早期诱导转录本EIIH,它编码一个353个氨基酸的蛋白质,该蛋白质具有一些特征,表明它可能是分泌型的或与膜结合的。EIIH与多种富含亮氨酸重复序列(LRR)的蛋白质也有较远的亲缘关系。胰岛素处理可增加哺乳大鼠、禁食成年大鼠和经链脲佐菌素(STZ)处理的糖尿病大鼠肝细胞中EIIH mRNA的水平,在这些大鼠中,胰岛素是维持EIIH表达基础水平所必需的。EIIH表达在哺乳/断奶过渡期被诱导,并在之后仍可检测到。成年大鼠的组织分布分析显示,其表达模式主要在肝脏、肠道和胰岛,与葡萄糖转运蛋白2(Glut2)的表达模式密切相关,表明它可能在碳水化合物代谢中发挥作用。EIIH可能是胰岛素转录调控的主要靶点,因此可能构成一个研究胰岛素作用于基因转录机制的新模型。

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