Ten nucleotide cis element in the 3′-untranslated region of the GLUT1 glucose transporter mRNA increases gene expression via mRNA stabilization

被引:48
|
作者
Boado, RJ [1 ]
Pardridge, WM
机构
[1] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USA
来源
MOLECULAR BRAIN RESEARCH | 1998年 / 59卷 / 01期
关键词
gene expression; blood-brain barrier; brain tumor; post-transcription; mRNA;
D O I
10.1016/S0169-328X(98)00134-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The GLUT1 glucose transporter gene is regulated at the post-transcriptional level, and a 10 nucleotide (nt) cis-acting element located at nt 2181-2190 of the GLUT1 3'-untranslated region (3'-UTR) increases the transient expression of a luciferase reporter gene. To investigate the role of this mRNA cis-element, stable transfectants expressing luciferase reporter genes were established in rat C6 glioma cells. Insertion of nt 2100-2300 of GLUT1 3'-UTR resulted in a marked increase in the abundance of both reporter gene mRNA and protein compared to the control, in parallel with a 228% increase in the mRNA t(1/2) determined with actinomycin D. Deletion of the 10 nt cis-acting element in the GLUT1 3'-UTR reduced the abundance of reporter gene products and the mRNA t(1/2) to levels similar to the control clone. Data suggest that the cis-acting element located at nt 2181-2190 of bovine GLUT1 mRNA 3'-UTR is responsible for increased GLUT1 gene expression via enhanced GLUT1 mRNA stabilization. (C) 1998 Elsevier Science B.V. All rights reserved.
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页码:109 / 113
页数:5
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