Abstract

The metabotropic glutamate receptor 5 (mGluR5) has a discrete tissue expression mainly limited to neural cells. Expression of mGluR5 is developmentally regulated and undergoes dramatic changes in association with neuropathological disorders. We report the complete genomic structure of the mGluR5 gene, which is composed of 11 exons and encompasses approximately 563 kbp. Three clusters of multiple transcription initiation sites located on three distinct exons (IA, IB, and II), which undergo alternative splicing, have been identified. The 5'-flanking regions of these exons were isolated and, using a luciferase reporter gene assay, shown to possess active promoter elements in SKN-MC neuroblastoma and U178-MG astroglioma cells. Promoter IA was characterized by a CpG island; promoter IB contained a TATA box, and promoter II possessed three active Oct-1-binding sites. Preferential luciferase activity was observed in SKN-MC concomitant with differential DNA binding activity to several responsive elements, including CREB, Oct-1, C/EBP, and Brn-2. Exposure to growth factors produced enhanced expression of promoters IB and II in astroglioma cells and activation of NF-kappa B. These results suggest that alternative 5'-splicing and usage of multiple promoters may contribute regulatory mechanisms for tissue- and context-specific expression of the mGluR5 gene.

Highlights

  • Glutamate, the main excitatory neurotransmitter in the brain, exerts a variety of physiological roles through the activation of multiple receptor proteins [1]

  • We report the complete genomic structure of the metabotropic glutamate receptor 5 (mGluR5) gene, which is composed of 11 exons and encompasses ϳ563 kbp

  • The transcriptionally competent regions for each promoter were determined by means of a luciferase reporter gene in both neuroblastoma and astroglioma cells; the cis regulatory elements within these promoter regions were identified based on gel-shift analysis

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Summary

Introduction

The main excitatory neurotransmitter in the brain, exerts a variety of physiological roles through the activation of multiple receptor proteins [1]. The 5؅-flanking regions of these exons were isolated and, using a luciferase reporter gene assay, shown to possess active promoter elements in SKN-MC neuroblastoma and U178-MG astroglioma cells.

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