Mediator protein mutations that selectively abolish activated transcription

被引:149
作者
Myers, LC
Gustafsson, CM
Hayashibara, KC
Brown, PO
Kornberg, RD [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Biol Struct, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[4] Univ Gothenburg, Sahlgrens Univ Hosp, Dept Clin Chem & Transfus Med, S-41345 Gothenburg, Sweden
关键词
D O I
10.1073/pnas.96.1.67
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
Deletion of any one of three subunits of the yeast Mediator of transcriptional regulation, Med2, Pgd1 (Hrs1), and Sin4, abolished activation by Ga14-VP16 in vitro. By contrast, other Mediator functions, stimulation of basal transcription and of TFIIH kinase activity, were unaffected, A different but overlapping Mediator subunit dependence was found for activation by Gcn4. The genetic requirements for activation in vivo were closely coincident with those in vitro. A whole genome expression profile of a Delta med2 strain showed diminished transcription of a subset of inducible genes but only minor effects on "basal" transcription. These findings make an important connection between transcriptional activation in vitro and in vivo, and identify Mediator as a "global" transcriptional coactivator.
引用
收藏
页码:67 / 72
页数:6
相关论文
共 40 条
[1]  
Ausubel F. M., 1994, CURRENT PROTOCOLS MO
[2]   GENETIC ISOLATION OF ADA2 - A POTENTIAL TRANSCRIPTIONAL ADAPTER REQUIRED FOR FUNCTION OF CERTAIN ACIDIC ACTIVATION DOMAINS [J].
BERGER, SL ;
PINA, B ;
SILVERMAN, N ;
MARCUS, GA ;
AGAPITE, J ;
REGIER, JL ;
TRIEZENBERG, SJ ;
GUARENTE, L .
CELL, 1992, 70 (02) :251-265
[3]   Genetics of transcriptional regulation in yeast: Connections to the RNA polymerase II CTD [J].
Carlson, M .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1997, 13 :1-23
[4]   TSF3, A GLOBAL REGULATORY PROTEIN THAT SILENCES TRANSCRIPTION OF YEAST GAL GENES, ALSO MEDIATES REPRESSION BY ALPHA-2 REPRESSOR AND IS IDENTICAL TO SIN4 [J].
CHEN, SM ;
WEST, RW ;
JOHNSON, SL ;
GANS, H ;
KRUGER, B ;
MA, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (02) :831-840
[5]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[6]   A MEDIATOR REQUIRED FOR ACTIVATION OF RNA POLYMERASE-II TRANSCRIPTION INVITRO [J].
FLANAGAN, PM ;
KELLEHER, RJ ;
SAYRE, MH ;
TSCHOCHNER, H ;
KORNBERG, RD .
NATURE, 1991, 350 (6317) :436-438
[7]   STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF THE SHORT ACIDIC TRANSCRIPTIONAL ACTIVATION REGION OF YEAST GCN4-PROTEIN [J].
HOPE, IA ;
MAHADEVAN, S ;
STRUHL, K .
NATURE, 1988, 333 (6174) :635-640
[8]  
Jackson BM, 1996, MOL CELL BIOL, V16, P5557
[9]   Mammalian mediator of transcriptional regulation and its possible role as an end-point of signal transduction pathways [J].
Jiang, YW ;
Veschambre, P ;
Erdjument-Bromage, H ;
Tempst, P ;
Conaway, JW ;
Conaway, RC ;
Kornberg, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8538-8543
[10]  
JIANG YW, 1995, GENETICS, V140, P103