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Glucokinase Gene Expression in Pancreatic Beta Cell

胰腺β细胞中的葡萄糖激酶基因表达

基本信息

批准号：
6905536
负责人：
MARK A MAGNUSON
金额：
$ 30.2万
依托单位：
VANDERBILT UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
1990
资助国家：
美国
起止时间：
1990-06-01 至 2007-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/6905536
关键词：
RNA splicing biological models blood glucose brain enzyme activity gene expression gene targeting genetically modified animals glucokinase glucose metabolism homeostasis insulin insulin receptor laboratory mouse model design /development noninsulin dependent diabetes mellitus pancreatic islet function

项目摘要

DESCRIPTION (provided by applicant): Knowledge of the mechanisms that modulate glucose-stimulated insulin secretion (GSIS) by pancreatic beta cells, particularly in the face of insulin resistance, is of paramount importance for understanding the pathogenesis of type 2 diabetes mellitus. Over the previous project period, it has become clear that even small changes in glucokinase (GK) activity in the pancreatic beta cell affect GSIS, that insulin action in the beta cell modulates GSIS, and that insulin affects GK gene expression, both at the transcriptional and post-translational levels. This proposal will explore several aspects of GK regulation and function. We will continue to place an emphasis both on the pancreatic beta cell, since it plays a principal role in most glycemic disorders and serves as a model for other glucose-sensitive cells, and on the generation of novel new mouse models. However, some studies will involve other sites of GK expression, such as the brain, in order to learn more about how the expression of GK in certain neurons contributes to the regulatory feedback loops that control the blood glucose concentration. In Aim 1 we will determine whether GK is necessary for neural glucose sensing by generating and characterizing brain-specific GK gene knockout mice. In Aim 2 we will establish true mouse models for PHHI and MODY-2 in order to correlate changes in enzyme kinetics with insuIin secretion and glucose homeostasis. In Aim 3 we will determine the role of alternate RNA processing the insulin receptor in modulating both GK gene transcription and subcellular localization in the pancreatic beta cell.

描述（由申请人提供）：了解胰腺β细胞调节葡萄糖刺激的胰岛素分泌（GSIS）的机制，特别是在胰岛素抵抗的情况下，对于理解2型糖尿病的发病机制至关重要。在前一个项目期间，已经清楚的是，即使是胰腺β细胞中葡萄糖激酶（GK）活性的微小变化也会影响GSIS，β细胞中的胰岛素作用调节GSIS，胰岛素在转录和翻译后水平上影响GK基因表达。本文将从几个方面探讨GK的调控和功能。我们将继续把重点放在胰腺β细胞，因为它在大多数血糖紊乱中起着主要作用，并作为其他葡萄糖敏感细胞的模型，并在新的新的小鼠模型的产生。然而，一些研究将涉及GK表达的其他部位，如大脑，以了解更多关于GK在某些神经元中的表达如何有助于控制血糖浓度的调节反馈回路。在目的1中，我们将通过产生和表征脑特异性GK基因敲除小鼠来确定GK是否是神经葡萄糖感知所必需的。目的2：建立PHHI和MODY-2的小鼠模型，以使酶动力学变化与胰岛素分泌和葡萄糖稳态相关。在目标3中，我们将确定交替RNA加工胰岛素受体在调节GK基因转录和胰腺β细胞亚细胞定位中的作用。

项目成果

期刊论文数量（29）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Variable expression of hepatic glucokinase in mice is due to a regulational locus that cosegregates with the glucokinase gene.

小鼠中肝葡萄糖激酶的可变表达是由于与葡萄糖激酶基因共分离的调节位点所致。

DOI：
10.1006/geno.1997.4936
发表时间：
1997
期刊：
Genomics.
影响因子：
0
作者：
Moates,JM;Postic,C;Decaux,JF;Girard,J;Magnuson,MA
通讯作者：
Magnuson,MA

Substrate-induced nuclear export and peripheral compartmentalization of hepatic glucokinase correlates with glycogen deposition.

DOI：
10.1155/edr.2001.173
发表时间：
2001-01-01
期刊：
International journal of experimental diabetes research
影响因子：
0
作者：
Jetton, T L;Shiota, M;Magnuson, M A
通讯作者：
Magnuson, M A

Cloning and characterization of the mouse glucokinase gene locus and identification of distal liver-specific DNase I hypersensitive sites.

DOI：
10.1006/geno.1995.9943
发表时间：
1995-10
期刊：
Genomics
影响因子：
4.4
作者：
Catherine Postic;K. D. Niswender;J. Decaux;Ramine Parsa;K. Shelton;Betty Gouhot;C. C. Pettepher-C.
通讯作者：
Catherine Postic;K. D. Niswender;J. Decaux;Ramine Parsa;K. Shelton;Betty Gouhot;C. C. Pettepher-C.

Nucleotide sequence of mouse SCIP cDNA, a POU-domain transcription factor.

小鼠 SCIP cDNA（一种 POU 域转录因子）的核苷酸序列。