Direct stimulation of transcription by negative cofactor 2 (NC2) through TATA-binding protein (TBP)

被引:43
作者
Cang, Y [1 ]
Prelich, G [1 ]
机构
[1] Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
关键词
BUR6; yeast;
D O I
10.1073/pnas.202236699
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Negative cofactor 2 (NC2) is an evolutionarily conserved transcriptional regulator that was originally identified as an inhibitor of basal transcription. its inhibitory mechanism has been extensively characterized; NC2 binds to the TATA-binding protein (TBP), blocking the recruitment of TFIIA and TFIIB, and thereby inhibiting preinitiation complex assembly. NC2 is also required for expression of many yeast genes in vivo and stimulates TATA-less transcription in a Drosophila in vitro transcription system, but the mechanism responsible for the NC2-mediated stimulation of transcription is not understood. Here we establish that yeast NC2 can directly stimulate activated transcription from TATA-driven promoters both in vivo and in vitro, and moreover that this positive role requires the same surface of TBP that mediates the NC2 repression activity. On the basis of these results, we propose a model to explain how NC2 can mediate both repression and activation through the same surface of TBP.
引用
收藏
页码:12727 / 12732
页数:6
相关论文
共 50 条
[1]   MOT1, A GLOBAL REPRESSOR OF RNA-POLYMERASE-II TRANSCRIPTION, INHIBITS TBP BINDING TO DNA BY AN ATP-DEPENDENT MECHANISM [J].
AUBLE, DT ;
HANSEN, KE ;
MUELLER, CGF ;
LANE, WS ;
THORNER, J ;
HAHN, S .
GENES & DEVELOPMENT, 1994, 8 (16) :1920-1934
[2]   The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAF(II)60 of Drosophila [J].
Burke, TW ;
Kadonaga, JT .
GENES & DEVELOPMENT, 1997, 11 (22) :3020-3031
[3]   The DPE, a conserved downstream core promoter element that is functionally analogous to the TATA box [J].
Burke, TW ;
Willy, PJ ;
Kutach, AK ;
Butler, JEF ;
Kadonaga, JT .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1998, 63 :75-82
[4]   Biochemistry and structural biology of transcription factor IID (TFIID) [J].
Burley, SK ;
Roeder, RG .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :769-799
[5]   A new regulatory domain on the TATA-binding protein [J].
Cang, Y ;
Auble, DT ;
Prelich, G .
EMBO JOURNAL, 1999, 18 (23) :6662-6671
[6]   2 DIFFERENTIALLY REGULATED MESSENGER-RNAS WITH DIFFERENT 5' ENDS ENCODE SECRETED AND INTRACELLULAR FORMS OF YEAST INVERTASE [J].
CARLSON, M ;
BOTSTEIN, D .
CELL, 1982, 28 (01) :145-154
[7]   The C-terminal domain-phosphorylated IIO form of RNA polymerase II is associated with the transcription repressor NC2 (Dr1/DRAP1) and is required for transcription activation in human nuclear extracts [J].
Castaño, E ;
Gross, P ;
Wang, ZX ;
Roeder, RG ;
Oelgeschläger, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7184-7189
[8]   Association of human TFIID-promoter complexes with silenced mitotic chromatin in vivo [J].
Christova, R ;
Oelgeschläger, T .
NATURE CELL BIOLOGY, 2002, 4 (01) :79-82
[9]   Mot1 activates and represses transcription by direct, ATPase-dependent mechanisms [J].
Dasgupta, A ;
Darst, RP ;
Martin, KJ ;
Afshari, CA ;
Auble, DT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) :2666-2671
[10]   Functional antagonism between RNA polymerase II holoenzyme and global negative regulator NC2 in vivo [J].
Gadbois, EL ;
Chao, DM ;
Reese, JC ;
Green, MR ;
Young, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :3145-3150