Cargando…

In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation

BACKGROUND: Subtypes of the GABA(A )receptor subunit exhibit diverse temporal and spatial expression patterns. In silico comparative analysis was used to predict transcriptional regulatory features in individual mammalian GABA(A )receptor subunit genes, and to identify potential transcriptional regu...

Descripción completa

Detalles Bibliográficos
Autor principal: Joyce, Christopher J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1934366/
https://www.ncbi.nlm.nih.gov/pubmed/17603907
http://dx.doi.org/10.1186/1471-2164-8-203
_version_ 1782134344213594112
author Joyce, Christopher J
author_facet Joyce, Christopher J
author_sort Joyce, Christopher J
collection PubMed
description BACKGROUND: Subtypes of the GABA(A )receptor subunit exhibit diverse temporal and spatial expression patterns. In silico comparative analysis was used to predict transcriptional regulatory features in individual mammalian GABA(A )receptor subunit genes, and to identify potential transcriptional regulatory components involved in the coordinate regulation of the GABA(A )receptor gene clusters. RESULTS: 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(A )receptor 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). CONCLUSION: The putative regulatory features identified by genomic analysis of GABA(A )receptor 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.
format Text
id pubmed-1934366
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-19343662007-07-28 In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation Joyce, Christopher J BMC Genomics Research Article BACKGROUND: Subtypes of the GABA(A )receptor subunit exhibit diverse temporal and spatial expression patterns. In silico comparative analysis was used to predict transcriptional regulatory features in individual mammalian GABA(A )receptor subunit genes, and to identify potential transcriptional regulatory components involved in the coordinate regulation of the GABA(A )receptor gene clusters. RESULTS: 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(A )receptor 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). CONCLUSION: The putative regulatory features identified by genomic analysis of GABA(A )receptor 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. BioMed Central 2007-06-30 /pmc/articles/PMC1934366/ /pubmed/17603907 http://dx.doi.org/10.1186/1471-2164-8-203 Text en Copyright © 2007 Joyce; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Joyce, Christopher J
In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation
title In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation
title_full In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation
title_fullStr In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation
title_full_unstemmed In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation
title_short In silico comparative genomic analysis of GABA(A )receptor transcriptional regulation
title_sort in silico comparative genomic analysis of gaba(a )receptor transcriptional regulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1934366/
https://www.ncbi.nlm.nih.gov/pubmed/17603907
http://dx.doi.org/10.1186/1471-2164-8-203
work_keys_str_mv AT joycechristopherj insilicocomparativegenomicanalysisofgabaareceptortranscriptionalregulation