In silico comparative genomic analysis of GABA_Areceptor transcriptional regulation

• Main Author: Joyce Christopher J
• Format: Article
• Language: English
• Published: BMC 2007-06-01
• Series: BMC Genomics
• Online Access: http://www.biomedcentral.com/1471-2164/8/203

<p>Abstract</p> <p>Background</p> <p>Subtypes of the GABA_Areceptor subunit exhibit diverse temporal and spatial expression patterns. <it>In silico </it>comparative analysis was used to predict transcriptional regulatory features in individual mammalian GABA_Areceptor subunit genes, and to identify potential transcriptional regulatory components involved in the coordinate regulation of the GABA_Areceptor gene clusters.</p> <p>Results</p> <p>Previously unreported putative promoters were identified for the β2, γ1, γ3, ε, θ and π subunit genes. Putative core elements and proximal transcriptional factors were identified within these predicted promoters, and within the experimentally determined promoters of other subunit genes. Conserved intergenic regions of sequence in the mammalian GABA_Areceptor gene cluster comprising the α1, β2, γ2 and α6 subunits were identified as potential long range transcriptional regulatory components involved in the coordinate regulation of these genes. A region of predicted DNase I hypersensitive sites within the cluster may contain transcriptional regulatory features coordinating gene expression. A novel model is proposed for the coordinate control of the gene cluster and parallel expression of the α1 and β2 subunits, based upon the selective action of putative Scaffold/Matrix Attachment Regions (S/MARs).</p> <p>Conclusion</p> <p>The putative regulatory features identified by genomic analysis of GABA_Areceptor genes were substantiated by cross-species comparative analysis and now require experimental verification. The proposed model for the coordinate regulation of genes in the cluster accounts for the head-to-head orientation and parallel expression of the α1 and β2 subunit genes, and for the disruption of transcription caused by insertion of a neomycin gene in the close vicinity of the α6 gene, which is proximal to a putative critical S/MAR.</p>