Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/27047
Title: Transcriptional regulation of the rat bradykinin B2 receptor gene: Identification of a silencer element
Authors: Baptista, Heloisa A.
Avellar, Maria CW
Araujo, Ronaldo C.
Pesquero, Jorge L.
Schanstra, Joost P.
Bascands, Jean L.
Esteve, Jean P.
Paiva, Antonio CM
Bader, Michael
Pesquero, João Bosco [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Univ Mogi Cruzes
Universidade Federal de Minas Gerais (UFMG)
Inst Louis Bugnard
Max Delbruck Ctr Mol Med
Issue Date: 1-Dec-2002
Publisher: Amer Soc Pharmacology Experimental Therapeutics
Citation: Molecular Pharmacology. Bethesda: Amer Soc Pharmacology Experimental Therapeutics, v. 62, n. 6, p. 1344-1355, 2002.
Abstract: Kinins are involved in a variety of physiological and pathophysiological processes related to cardiovascular homeostasis, inflammation, blood flow, and nociception. Under physiological conditions, the bradykinin B2 (BKB2) receptor is constitutively expressed and mediates most of kinins' actions. However, the mechanisms regulating BKB2 receptor gene expression are still poorly understood. in this study, 4.6 kilobases of the 5'-flanking region from the rat BKB2 receptor gene were sequenced, and computer analysis revealed several sites for transcriptional factors. Nine promoter mutants were cloned in luciferase reporter gene vectors and transfected in NG108-15 cells and rat aorta vascular smooth muscle cells (VSMCs), showing several positive and negative regulatory elements. A classical silencer with 56 base pairs (bp) caused a decrease in reporter gene activity in NG108-15 cells and VSMCs and was able to inhibit the thymidine kinase promoter. Using electrophoretic mobility shift assay and surface plasmon resonance assay, protein-DNA interactions in the silencer region were determined and specific sets of protein-silencer complexes were detected in both cell types. More intense complexes were observed in the central 21 bp of the silencer and mutation in a putative SRE-1 site strongly impaired the protein-DNA binding. Down-regulation of the BKB2 receptor population in NG108-15 cells promoted by N-6, 2'-O-dibutyryladenosine 3':5'-cyclic monophosphate was paralleled by an increase in the amount of nuclear proteins bound to the silencer sequence showing an inverse relationship between protein-silencer complexes and the transcription of the BKB2 receptor gene. in summary, these data highlight the cell-specific regulation of the BKB2 receptor and the importance of a silencer element present in the regulatory region of the gene.
URI: http://repositorio.unifesp.br/handle/11600/27047
ISSN: 0026-895X
Other Identifiers: http://dx.doi.org/10.1124/mol.62.6.1344
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.


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