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Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene

The sarco(endo)plasmic reticulum Ca-ATPases (SERCAs) belong to a family of active calcium transport enzymes encoded by the SERCA1, 2, and 3 genes. In this study, we describe the complete structure of the human SERCA2 gene and its 5’ -regulatory region. The hSERCA2 gene is located in chromosome 12 po...

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Autores principales: Zarain-Herzberg, Angel, Alvarez-Fernandez, Georgina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009281/
https://www.ncbi.nlm.nih.gov/pubmed/12805933
http://dx.doi.org/10.1100/tsw.2002.228
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author Zarain-Herzberg, Angel
Alvarez-Fernandez, Georgina
author_facet Zarain-Herzberg, Angel
Alvarez-Fernandez, Georgina
author_sort Zarain-Herzberg, Angel
collection PubMed
description The sarco(endo)plasmic reticulum Ca-ATPases (SERCAs) belong to a family of active calcium transport enzymes encoded by the SERCA1, 2, and 3 genes. In this study, we describe the complete structure of the human SERCA2 gene and its 5’ -regulatory region. The hSERCA2 gene is located in chromosome 12 position q24.1 in Contig NT_009770.8, spans 70 kb, and is organized in 21 exons intervened by 20 introns. The last two exons of the pre-mRNA produce by alternatively splicing the cardiac/slow-twitch muscle-specific SERCA2a isoform and the ubiquitous SERCA2b isoform. The sequence of the proximal 225-bp regulatory region of the SERCA2 genes is 80% G+C-rich and is conserved among human, rabbit, rat, and mouse species. It contains a TATA-like-box, an E-box/USF sequence, a CAAT-box, four Sp1 binding sites, and a thyroid hormone responsive element (TRE). There are two other conserved regulatory regions located between positions -410 to -661 bp and from -919 to -1410 bp. Among the DNA cis-elements present in these two regulatory regions there are potential binding sites for: GATA-4, -5, -6, Nkx-2.5/Csx, OTF-1, USF, MEF-2, SRF, PPAR/RXR, AP-2, and TREs. Upstream from position -1.5 kb, there is no significant homology among the SERCA2 genes cloned. In addition, the human gene has several repeated sequences mainly of the Alu and L2 type located upstream from position -1.7 kb, spanning in a continuous fashion for more than 40 kb. In this study, we report the cloning of 2.4 kb of 5’-regulatory region and demonstrate that the proximal promoter region is sufficient for expression in cardiac myocytes, and the region from -225 to -1232 bp contains regulatory DNA elements which down-regulate the expression of the SERCA2 gene in neonatal cardiomyocytes.
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spelling pubmed-60092812018-07-04 Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene Zarain-Herzberg, Angel Alvarez-Fernandez, Georgina ScientificWorldJournal Research Article The sarco(endo)plasmic reticulum Ca-ATPases (SERCAs) belong to a family of active calcium transport enzymes encoded by the SERCA1, 2, and 3 genes. In this study, we describe the complete structure of the human SERCA2 gene and its 5’ -regulatory region. The hSERCA2 gene is located in chromosome 12 position q24.1 in Contig NT_009770.8, spans 70 kb, and is organized in 21 exons intervened by 20 introns. The last two exons of the pre-mRNA produce by alternatively splicing the cardiac/slow-twitch muscle-specific SERCA2a isoform and the ubiquitous SERCA2b isoform. The sequence of the proximal 225-bp regulatory region of the SERCA2 genes is 80% G+C-rich and is conserved among human, rabbit, rat, and mouse species. It contains a TATA-like-box, an E-box/USF sequence, a CAAT-box, four Sp1 binding sites, and a thyroid hormone responsive element (TRE). There are two other conserved regulatory regions located between positions -410 to -661 bp and from -919 to -1410 bp. Among the DNA cis-elements present in these two regulatory regions there are potential binding sites for: GATA-4, -5, -6, Nkx-2.5/Csx, OTF-1, USF, MEF-2, SRF, PPAR/RXR, AP-2, and TREs. Upstream from position -1.5 kb, there is no significant homology among the SERCA2 genes cloned. In addition, the human gene has several repeated sequences mainly of the Alu and L2 type located upstream from position -1.7 kb, spanning in a continuous fashion for more than 40 kb. In this study, we report the cloning of 2.4 kb of 5’-regulatory region and demonstrate that the proximal promoter region is sufficient for expression in cardiac myocytes, and the region from -225 to -1232 bp contains regulatory DNA elements which down-regulate the expression of the SERCA2 gene in neonatal cardiomyocytes. TheScientificWorldJOURNAL 2002-05-29 /pmc/articles/PMC6009281/ /pubmed/12805933 http://dx.doi.org/10.1100/tsw.2002.228 Text en Copyright © 2002 Angel Zarain-Herzberg and Georgina Alvarez-Fernandez. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zarain-Herzberg, Angel
Alvarez-Fernandez, Georgina
Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene
title Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene
title_full Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene
title_fullStr Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene
title_full_unstemmed Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene
title_short Sarco(endo)plasmic Reticulum Ca-ATPase-2 Gene: Structure and Transcriptional Regulation of the Human Gene
title_sort sarco(endo)plasmic reticulum ca-atpase-2 gene: structure and transcriptional regulation of the human gene
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009281/
https://www.ncbi.nlm.nih.gov/pubmed/12805933
http://dx.doi.org/10.1100/tsw.2002.228
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