Molecular cloning and functional analysis of the murine bax gene promoter

Citation
E. Igata et al., Molecular cloning and functional analysis of the murine bax gene promoter, GENE, 238(2), 1999, pp. 407-415
Citations number
21
Categorie Soggetti
Molecular Biology & Genetics
Journal title
GENE
ISSN journal
03781119 → ACNP
Volume
238
Issue
2
Year of publication
1999
Pages
407 - 415
Database
ISI
SICI code
0378-1119(19991001)238:2<407:MCAFAO>2.0.ZU;2-K
Abstract
Bcl-2-associated X protein (Bax) is a proapoptotic protein and is suggested to have an important role in carcinogenesis. To investigate the mechanism of bar gene transcriptional regulation, we isolated and sequenced the genom ic DNA fragment of the 5' flanking region of the murine bur gene, and subcl oned its promoter region into a luciferase reporter construction. The murin e bur promoter is TATA-less, and the sequence is only partially homologous to that of the human bar promoter. Transient transfection into NIH 3T3 cell s using unidirectionally deleted promoters and mutants of Spl sites reveale d that two Spl sites were partially responsible for the basal activity. The murine bar promoter was not responsive to exogenous p53, suggesting that t he p53-responsive element may not exist in the region used in our current e xperiments. (C) 1999 Elsevier Science B.V. All rights reserved.