Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/114
Title: Sp1/3 and NF-1 mediate basal transcription of the human P2X1 gene in megakaryoblastic MEG-01 cells
Authors: Zhao, Jiangqin
Ennion, Steven J.
First Published: 10-Mar-2006
Publisher: Biomed Central Ltd
Citation: BMC Molecular Biology, 2006, 7:10
Abstract: Background: P2X[subscript 1] receptors play an important role in platelet function as they can induce shape change, granule centralization and are also involved in thrombus formation. As platelets have no nuclei, the level of P2X[subscript 1] expression depends on transcriptional regulation in megakaryocytes, the platelet precursor cell. Since nothing is known about the molecular mechanisms regulating megakaryocytic P2X[subscript 1] expression, this study aimed to identify and functionally characterize the P2X[subscript 1] core promoter utilized in the human megakaryoblastic cell line MEG-01. Results: In order to identify cis-acting elements involved in the transcriptional regulation of P2X[subscript 1] expression, the ability of 4.7 kb P2X[subscript 1] upstream sequence to drive luciferase reporter gene expression was tested. Low promoter activity was detected in proliferating MEG-01 cells. This activity increased 20-fold after phorbol-12-myristate-13-acetate (PMA) induced differentiation. A transcription start site was detected 365 bp upstream of the start codon by primer extension. Deletion analysis of reporter constructs indicated a core promoter located within the region -68 to +149 bp that contained two Sp1 sites (named Sp1a and Sp1b) and an NF-1 site. Individual mutations of Sp1b or NF-1 binding sites severely reduced promoter activity whereas triple mutation of Sp1a, Sp1b and NF-1 sites completely abolished promoter activity in both untreated and PMA treated cells. Sp1/3 and NF-1 proteins were shown to bind their respective sites by EMSA and interaction of Sp1/3, NF-1 and TFIIB with the endogenous P2X[subscript 1] core promoter in MEG-01 cells was demonstrated by chromatin immunoprecipitation. Alignment of P2X[subscript 1] genes from human, chimp, rat, mouse and dog revealed consensus Sp1a, Sp1b and NF-1 binding sites in equivalent positions thereby demonstrating evolutionary conservation of these functionally important sites. Conclusion: This study has identified and characterized the P2X[subscript 1] promoter utilized in MEG-01 cells and shown that binding of Sp1/3 and NF-1 to elements in the direct vicinity of the transcription start site is essential for basal transcription. Targeting the function of these transcription factors in megakaryocytes may therefore provide a basis for the future therapeutic manipulation of platelet P2X[subscript 1] function.
DOI Link: 10.1186/1471-2199-7-10
eISSN: 1471-2199
Links: http://hdl.handle.net/2381/114
http://www.biomedcentral.com/1471-2199/7/10
Version: Publisher version
Status: Peer reviewed
Type: Article
Rights: Copyright © 2006Zhao and Ennion; licensee BioMed Central Ltd. 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.
Appears in Collections:Published Articles, Dept. of Cell Physiology and Pharmacology

Files in This Item:
File Description SizeFormat 
1471-2199-7-10.pdf909.36 kBAdobe PDFView/Open


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.