Transcriptional regulation of neuronal nicotinic acetylcholine receptor genes - Functional interactions between Sp1 and the rat beta 4 subunit gene promoter

被引:31
作者
Bigger, CB [1 ]
Casanova, EA [1 ]
Gardner, PD [1 ]
机构
[1] UNIV TEXAS,HLTH SCI CTR,INST BIOTECHNOL,CTR MOL MED,SAN ANTONIO,TX 78245
关键词
D O I
10.1074/jbc.271.51.32842
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To date, 11 members (alpha 2-alpha 9 and beta 2-beta 4) of the neuronal nicotinic acetylcholine receptor gene family have been identified. These genes encode subunits that form distinct receptors with different pharmacological and physiological profiles in temporally and spatially restricted patterns within the nervous system, Distinct molecular mechanisms probably orchestrate the expression of various receptor subtypes, yet little is known of specific transcriptional regulatory elements and their associated factors that are responsible for this segregated pattern of expression, Here we report the identification of an element, in the 5'-flanking region of the rat beta 4 subunit gene, containing a CA box that is necessary for beta 4 promoter activity in a transiently transfected cholinergic cell line, SN17. This element was shown to interact with a protein(s) in SN17 nuclear extracts that is antigenically related to the transcriptional activator Sp1. Furthermore, co-transfection experiments confirmed that Sp1 can transactivate a beta 4 promoter-reporter gene construct, indicating that Sp1 is necessary, at least in part, for transcriptional activation of the beta 4 subunit gene.
引用
收藏
页码:32842 / 32848
页数:7
相关论文
共 69 条
[1]  
AMADOR M, 1995, J NEUROSCI, V15, P4525
[2]   NEGATIVE REGULATORY ELEMENTS UPSTREAM OF A NOVEL EXON OF THE NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTOR ALPHA-2 SUBUNIT GENE [J].
BESSIS, A ;
SAVATIER, N ;
DEVILLERSTHIERY, A ;
BEJANIN, S ;
CHANGEUX, JP .
NUCLEIC ACIDS RESEARCH, 1993, 21 (09) :2185-2192
[3]   TRANSCRIPTIONAL INITIATION IS CONTROLLED BY UPSTREAM GC-BOX INTERACTIONS IN A TATAA-LESS PROMOTER [J].
BLAKE, MC ;
JAMBOU, RC ;
SWICK, AG ;
KAHN, JW ;
AZIZKHAN, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) :6632-6641
[4]  
BOISCLAIR YR, 1993, J BIOL CHEM, V268, P24892
[5]   FUNCTIONAL EXPRESSION OF 2 NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTORS FROM CDNA CLONES IDENTIFIES A GENE FAMILY [J].
BOULTER, J ;
CONNOLLY, J ;
DENERIS, E ;
GOLDMAN, D ;
HEINEMANN, S ;
PATRICK, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7763-7767
[6]   ISOLATION OF A CDNA CLONE CODING FOR A POSSIBLE NEURAL NICOTINIC ACETYLCHOLINE-RECEPTOR ALPHA-SUBUNIT [J].
BOULTER, J ;
EVANS, K ;
GOLDMAN, D ;
MARTIN, G ;
TRECO, D ;
HEINEMANN, S ;
PATRICK, J .
NATURE, 1986, 319 (6052) :368-374
[7]  
BOULTER J, 1990, J BIOL CHEM, V265, P4472
[8]  
CHEN HM, 1993, J BIOL CHEM, V268, P8230
[9]  
CHEN XR, 1992, ONCOGENE, V7, P1805
[10]   REGULATION OF TRANSCRIPTION OF THE HUMAN ERYTHROPOIETIN RECEPTOR GENE BY PROTEINS BINDING TO GATA-1 AND SP1 MOTIFS [J].
CHIN, K ;
ODA, N ;
SHEN, K ;
NOGUCHI, CT .
NUCLEIC ACIDS RESEARCH, 1995, 23 (15) :3041-3049