Corti Corrado, Clarkson Richard W E, Crepaldi Luca, Sala Cinzia F, Xuereb John H, Ferraguti Francesco
Cambridge Brain Bank Laboratory, Department of Pathology, University of Cambridge, Level 3 Laboratory Block Addenbrooke's Hospital, Hills Road, CB2 2QQ Cambridge, United Kingdom.
J Biol Chem. 2003 Aug 29;278(35):33105-19. doi: 10.1074/jbc.M212380200. Epub 2003 Jun 3.
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.
代谢型谷氨酸受体5(mGluR5)具有离散的组织表达,主要局限于神经细胞。mGluR5的表达受发育调控,并与神经病理疾病相关发生显著变化。我们报告了mGluR5基因的完整基因组结构,该基因由11个外显子组成,约含563千碱基对。已鉴定出位于三个不同外显子(IA、IB和II)上的三个多转录起始位点簇,这些外显子会发生可变剪接。分离出这些外显子的5'侧翼区域,并通过荧光素酶报告基因检测表明,它们在SKN-MC神经母细胞瘤和U178-MG星形胶质瘤细胞中具有活性启动子元件。启动子IA的特征是有一个CpG岛;启动子IB含有一个TATA盒,启动子II有三个活性Oct-1结合位点。在SKN-MC中观察到了优先的荧光素酶活性,同时伴随着对包括CREB、Oct-1、C/EBP和Brn-2在内的几个反应元件的不同DNA结合活性。暴露于生长因子会使星形胶质瘤细胞中启动子IB和II的表达增强,并激活NF-κB。这些结果表明,5'端可变剪接和多个启动子的使用可能为mGluR5基因的组织特异性和背景特异性表达提供调控机制。