CLONING OF GT BOX-BINDING PROTEINS - A NOVEL SP1 MULTIGENE FAMILY REGULATING T-CELL RECEPTOR GENE-EXPRESSION

被引:546
作者
KINGSLEY, C
WINOTO, A
机构
[1] UNIV CALIF BERKELEY,DEPT MOLEC & CELL BIOL,DIV IMMUNOL,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY,CANC RES LAB,BERKELEY,CA 94720
关键词
D O I
10.1128/MCB.12.10.4251
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
Analysis of a T-cell antigen receptor (TCR) alpha promoter from a variable gene segment (V) revealed a critical GT box element which is also found in upstream regions of several Valpha genes, TCR enhancer, and regulatory elements of other genes. This element is necessary for TCR gene expression and binds several proteins. These GT box-binding proteins were identified as members of a novel Spl multigene family. Two of them, which we term Sp2 and Sp3, were cloned. Sp2 and Sp3 contain zinc fingers and transactivation domains similar to those of Sp1. Like Sp1, Sp2 and Sp3 are expressed ubiquitously, and their in vitro-translated products bind to the GT box in TCR Valpha promoters. Sp3, in particular, also binds to the Spl consensus sequence GC box and has binding activity similar to that of Sp1. As the GT box has also previously been shown to play a role in gene regulation of other genes, these newly isolated Sp2 and Sp3 proteins might regulate expression not only of the TCR gene but of other genes as well.
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页码:4251 / 4261
页数:11
相关论文
共 40 条
[1]   TRANSCRIPTION FROM A MURINE T-CELL RECEPTOR V-BETA PROMOTER DEPENDS ON A CONSERVED DECAMER MOTIF SIMILAR TO THE CYCLIC-AMP RESPONSE ELEMENT [J].
ANDERSON, SJ ;
MIYAKE, S ;
LOH, DY .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :4835-4845
[2]   A CONSERVED SEQUENCE IN THE T-CELL RECEPTOR BETA-CHAIN PROMOTER REGION [J].
ANDERSON, SJ ;
CHOU, HS ;
LOH, DY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (10) :3551-3554
[3]   SYNERGISTIC ACTIVATION BY THE GLUTAMINE-RICH DOMAINS OF HUMAN TRANSCRIPTION FACTOR SP1 [J].
COUREY, AJ ;
HOLTZMAN, DA ;
JACKSON, SP ;
TJIAN, R .
CELL, 1989, 59 (05) :827-836
[4]   ANALYSIS OF SP1 INVIVO REVEALS MULTIPLE TRANSCRIPTIONAL DOMAINS, INCLUDING A NOVEL GLUTAMINE-RICH ACTIVATION MOTIF [J].
COUREY, AJ ;
TJIAN, R .
CELL, 1988, 55 (05) :887-898
[5]   T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION [J].
DAVIS, MM ;
BJORKMAN, PJ .
NATURE, 1988, 334 (6181) :395-402
[6]   TRANSFER OF SPECIFICITY BY MURINE ALPHA-T-CELL AND BETA-T-CELL RECEPTOR GENES [J].
DEMBIC, Z ;
HAAS, W ;
WEISS, S ;
MCCUBREY, J ;
KIEFER, H ;
VONBOEHMER, H ;
STEINMETZ, M .
NATURE, 1986, 320 (6059) :232-238
[7]   SEPARATE ELEMENTS CONTROL DJ AND VDJ REARRANGEMENT IN A TRANSGENIC RECOMBINATION SUBSTRATE [J].
FERRIER, P ;
KRIPPL, B ;
BLACKWELL, TK ;
FURLEY, AJW ;
SUH, HK ;
WINOTO, A ;
COOK, WD ;
HOOD, L ;
COSTANTINI, F ;
ALT, FW .
EMBO JOURNAL, 1990, 9 (01) :117-125
[8]  
FERRIER P, 1989, COLD SPRING HARB SYM, V1, P191
[9]   CORRELATIONS BETWEEN T-CELL SPECIFICITY AND THE STRUCTURE OF THE ANTIGEN RECEPTOR [J].
FINK, PJ ;
MATIS, LA ;
MCELLIGOTT, DL ;
BOOKMAN, M ;
HEDRICK, SM .
NATURE, 1986, 321 (6067) :219-226
[10]   UNUSUAL ORGANIZATION AND DIVERSITY OF T-CELL RECEPTOR ALPHA-CHAIN GENES [J].
HAYDAY, AC ;
DIAMOND, DJ ;
TANIGAWA, G ;
HEILIG, JS ;
FOLSOM, V ;
SAITO, H ;
TONEGAWA, S .
NATURE, 1985, 316 (6031) :828-832