THE GENERAL TRANSCRIPTION FACTOR RAP30 BINDS TO RNA POLYMERASE-II AND PREVENTS IT FROM BINDING NONSPECIFICALLY TO DNA

被引:73
作者
KILLEEN, MT
GREENBLATT, JF
机构
[1] UNIV TORONTO,DEPT MOLEC & MED GENET,TORONTO M5G 1L6,ONTARIO,CANADA
[2] UNIV TORONTO,CHARLES H BEST INST,DEPT BANTING & BEST,TORONTO M5G 1L6,ONTARIO,CANADA
关键词
D O I
10.1128/MCB.12.1.30
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
RAP30/74 is a human general transcription factor that binds to RNA polymerase II and is required for initiation of transcription in vitro regardless of whether the promoter has a recognizable TATA box (Z. F. Burton, M. Killeen, M. Sopta, L. G. Ortolan, and J. F. Greenblatt, Mol. Cell. Biol. 8:1602-1613, 1988). Part of the amino acid sequence of RAP30, the small subunit of RAP30/74, has limited homology with part of Escherichia coli sigma-70 (M. Sopta, Z. F. Burton, and J. Greenblatt, Nature (London) 341:410-414, 1989). To determine which sigmalike activities of RAP30/74 could be attributed to RAP30, we purified human RAP30 and a RAP30-glutathione-S-transferase fusion protein that had been produced in E. coli. Bacterially produced RAP30 bound to RNA polymerase II in the absence of RAP74. Both partially purified natural RAP30/74 and recombinant RAP30 prevented RNA polymerase II from binding nonspecifically to DNA. In addition, nonspecific transcription by RNA polymerase II was greatly inhibited by RAP30-glutathione-S-transferase. DNA-bound RNA polymerase II could be removed from DNA by partially purified RAP30/74 but not by bacterially expressed RAP30. Thus, the ability of RAP30/74 to recruit RNA polymerase II to a promoter-bound preinitiation complex may be an indirect consequence of its ability to suppress nonspecific binding of RNA polymerase II to DNA.
引用
收藏
页码:30 / 37
页数:8
相关论文
共 48 条
[41]   TRANSCRIPTIONAL ACTIVATION BY SP1 AS DIRECTED THROUGH TATA OR INITIATOR - SPECIFIC REQUIREMENT FOR MAMMALIAN TRANSCRIPTION FACTOR-IID [J].
SMALE, ST ;
SCHMIDT, MC ;
BERK, AJ ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4509-4513
[42]   SINGLE-STEP PURIFICATION OF POLYPEPTIDES EXPRESSED IN ESCHERICHIA-COLI AS FUSIONS WITH GLUTATHIONE S-TRANSFERASE [J].
SMITH, DB ;
JOHNSON, KS .
GENE, 1988, 67 (01) :31-40
[43]  
SOPTA M, 1985, J BIOL CHEM, V260, P353
[44]   STRUCTURE AND ASSOCIATED DNA-HELICASE ACTIVITY OF A GENERAL TRANSCRIPTION INITIATION-FACTOR THAT BINDS TO RNA POLYMERASE-II [J].
SOPTA, M ;
BURTON, ZF ;
GREENBLATT, J .
NATURE, 1989, 341 (6241) :410-414
[45]  
STAGIER P, 1985, FEBS LETT, V187, P11
[46]   FACTORS INVOLVED IN SPECIFIC TRANSCRIPTION BY MAMMALIAN RNA POLYMERASE-II - IDENTIFICATION OF GENERAL TRANSCRIPTION FACTOR TFIIG [J].
SUMIMOTO, H ;
OHKUMA, Y ;
YAMAMOTO, T ;
HORIKOSHI, M ;
ROEDER, RG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9158-9162
[47]   PHYSICAL ANALYSIS OF TRANSCRIPTION PREINITIATION COMPLEX ASSEMBLY ON A CLASS-II GENE PROMOTER [J].
VANDYKE, MW ;
ROEDER, RG ;
SAWADOGO, M .
SCIENCE, 1988, 241 (4871) :1335-1338
[48]   MUTATION CHANGING THE SPECIFICITY OF AN RNA-POLYMERASE SIGMA-FACTOR [J].
ZUBER, P ;
HEALY, J ;
CARTER, HL ;
CUTTING, S ;
MORAN, CP ;
LOSICK, R .
JOURNAL OF MOLECULAR BIOLOGY, 1989, 206 (04) :605-614