Suppr超能文献

葡萄糖-6-磷酸酶催化亚基信使核糖核酸的表达与分布及其在糖尿病状态下的变化

Expression and distribution of glucose-6-phosphatase catalytic subunit messenger RNA and its changes in the diabetic state.

作者信息

Shingu R, Nakajima H, Horikawa Y, Hamaguchi T, Yamasaki T, Miyagawa J, Namba M, Hanafusa T, Matsuzawa Y

机构信息

Second Department of Internal Medicine, Osaka University Medical School, Suita, Japan.

出版信息

Res Commun Mol Pathol Pharmacol. 1996 Jul;93(1):13-24.

PMID:8865366
Abstract

Glucose-6-phosphatase (G6Pase) plays a major role in gluconeogenic pathway. To analyze its regulation, we have cloned a full-length cDNA for G6Pase catalytic subunit from the rat liver. In the cloned cDNA, a 492 base insertion, respective to the previously reported sequence, was found in the 3'-noncoding region. In both ends of this insertion, 5'- and 3' 2' splice site motifs were identified. However, spliced mRNA was hardly observed in the rat RNA. Abundant expression was observed in the liver and the kidney by Northern analysis. Expression was also observed in the spleen, adrenal gland and small intestines. Reverse-transcription (RT) polymerase chain reaction (PCR) analysis revealed that G6Pase mRNA was also expressed in a variety of tissues including pancreatic islets. Its expression was increased in the ketotic diabetic mice livers and was corrected by insulin treatment. However, no appreciable changes were observed in kidneys. Broad tissue distribution in expression and the tissue specificity in regulation were thus considered to be the important features of G6Pase gene.

摘要

葡萄糖-6-磷酸酶(G6Pase)在糖异生途径中起主要作用。为了分析其调控机制,我们从大鼠肝脏中克隆了G6Pase催化亚基的全长cDNA。在克隆的cDNA中,在3'-非编码区发现了一个相对于先前报道序列的492个碱基的插入片段。在该插入片段的两端,鉴定出了5'-和3' 2'剪接位点基序。然而,在大鼠RNA中几乎未观察到剪接后的mRNA。通过Northern分析在肝脏和肾脏中观察到丰富的表达。在脾脏、肾上腺和小肠中也观察到表达。逆转录(RT)聚合酶链反应(PCR)分析表明,G6Pase mRNA也在包括胰岛在内的多种组织中表达。其在酮症糖尿病小鼠肝脏中的表达增加,并通过胰岛素治疗得到纠正。然而,在肾脏中未观察到明显变化。因此,广泛的组织表达分布和调控中的组织特异性被认为是G6Pase基因的重要特征。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验