E2F-mediated growth regulation requires transcription factor cooperation

被引:58
作者
vanGinkel, PR [1 ]
Hsiao, KM [1 ]
Schjerven, H [1 ]
Farnham, PJ [1 ]
机构
[1] UNIV WISCONSIN,MCARDLE LAB CANC RES,SCH MED,MADISON,WI 53706
关键词
D O I
10.1074/jbc.272.29.18367
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
Previous studies have indicated that the presence of an E2F site is not sufficient for G(1)/S phase transcriptional regulation, For example, the E2F sites in the E2F1 promoter are necessary, but not sufficient, to mediate differential promoter activity in G(0) and S phase, We have now utilized the E2F1 minimal promoter to test several hypotheses that could account for these observations, To test the hypothesis that G(1)/S phase regulation is achieved via E2F-mediated repression of a strong promoter, a variety of transactivation domains were brought to the E2F1 minimal promoter, Although many of these factors caused increased promoter activity, growth regulation was not observed, suggesting that a general repression model is incorrect. However, constructs having CCAAT or YY1 sites or certain GC boxes cloned upstream of the E2F1 minimal promoter displayed E2F site-dependent regulation, Further analysis of the promoter activity suggested that E2F requires cooperation with another factor to activate transcription in S phase, However, we found that the requirement for E2F to cooperate with additional factors to achieve growth regulation could be relieved by bringing the E2F1 activation domain to the promoter via a Gal4 DNA binding domain, Our results suggest a model that explains why some, but not all, promoters that contain E2F sites display growth regulation.
引用
收藏
页码:18367 / 18374
页数:8
相关论文
共 40 条
[1]   A RAPID MICROPREPARATION TECHNIQUE FOR EXTRACTION OF DNA-BINDING PROTEINS FROM LIMITING NUMBERS OF MAMMALIAN-CELLS [J].
ANDREWS, NC ;
FALLER, DV .
NUCLEIC ACIDS RESEARCH, 1991, 19 (09) :2499-2499
[2]   E2F-4, A NEW MEMBER OF THE E2F GENE FAMILY, HAS ONCOGENIC ACTIVITY AND ASSOCIATES WITH P107 IN-VIVO [J].
BEIJERSBERGEN, RL ;
KERKHOVEN, RM ;
ZHU, LA ;
CARLEE, L ;
VOORHOEVE, PM ;
BERNARDS, R .
GENES & DEVELOPMENT, 1994, 8 (22) :2680-2690
[3]  
Blau J, 1996, MOL CELL BIOL, V16, P2044
[4]   HUMAN CCAAT-BINDING PROTEINS HAVE HETEROLOGOUS SUBUNITS [J].
CHODOSH, LA ;
BALDWIN, AS ;
CARTHEW, RW ;
SHARP, PA .
CELL, 1988, 53 (01) :11-24
[5]   A MULTIPLICITY OF CCAAT BOX-BINDING PROTEINS [J].
DORN, A ;
BOLLEKENS, J ;
STAUB, A ;
BENOIST, C ;
MATHIS, D .
CELL, 1987, 50 (06) :863-872
[6]   ROLE OF A PROXIMAL NF-Y BINDING PROMOTER ELEMENT IN S-PHASE-SPECIFIC EXPRESSION OF MOUSE RIBONUCLEOTIDE REDUCTASE R2 GENE [J].
FILATOV, D ;
THELANDER, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :25239-25243
[7]   Position-dependent transcriptional regulation of the murine dihydrofolate reductase promoter by the E2F transactivation domain [J].
Fry, CJ ;
Slansky, JE ;
Farnham, PJ .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (04) :1966-1976
[8]   A TRANSCRIPTIONALLY ACTIVE DNA-BINDING SITE FOR HUMAN P53 PROTEIN COMPLEXES [J].
FUNK, WD ;
PAK, DT ;
KARAS, RH ;
WRIGHT, WE ;
SHAY, JW .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) :2866-2871
[9]   HOMOLOGOUS RECOGNITION OF A PROMOTER DOMAIN COMMON TO THE MSV LTR AND THE HSV TK GENE [J].
GRAVES, BJ ;
JOHNSON, PF ;
MCKNIGHT, SL .
CELL, 1986, 44 (04) :565-576
[10]   SP1-MEDIATED TRANSCRIPTIONAL ACTIVATION IS REPRESSED BY SP3 [J].
HAGEN, G ;
MULLER, S ;
BEATO, M ;
SUSKE, G .
EMBO JOURNAL, 1994, 13 (16) :3843-3851