A DOWNSTREAM-ELEMENT-BINDING FACTOR FACILITATES ASSEMBLY OF A FUNCTIONAL PREINITIATION COMPLEX AT THE SIMIAN VIRUS-40 MAJOR LATE PROMOTER

被引:43
作者
AYER, DE [1 ]
DYNAN, WS [1 ]
机构
[1] UNIV COLORADO,DEPT CHEM & BIOCHEM,CAMPUS BOX 215,BOULDER,CO 80309
关键词
D O I
10.1128/MCB.10.7.3635
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
Recent work has shown that many promoters recognized by eucaryotic RNA polymerase II contain essential sequences located downstream of the transcriptional initiation site. We show here that the activity of a promoter element centered 28 base pairs downstream of the simian virus 40 major late initiation site appears to be mediated by a DNA-binding protein, which was isolated by affinity chromatography from HeLa cell nuclear extracts. In the absence of the other components of the transcriptional machinery, the protein bound specifically but weakly to its recognition sequence, with a Kd of approximately 10-8 M. Analysis of kinetic data showed that mutation of the downstream element decreased the number of functional preinitiation complexes assembled at the promoter without significantly altering the time required for half the complexes to assemble. This suggests that in the absence of the downstream activating protein, preinitiation complexes are at least partially assembled but are not transcriptionally competent.
引用
收藏
页码:3635 / 3645
页数:11
相关论文
共 61 条
[1]  
[Anonymous], 1969, DATA REDUCTION ERROR
[2]  
ARIAS JA, 1989, J BIOL CHEM, V264, P3223
[3]   LOCALIZATION OF TRANSCRIPTIONAL REGULATORY ELEMENTS AND NUCLEAR FACTOR BINDING-SITES IN MOUSE RIBOSOMAL-PROTEIN GENE RPL32 [J].
ATCHISON, ML ;
MEYUHAS, O ;
PERRY, RP .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (05) :2067-2074
[4]   SIMIAN VIRUS-40 MAJOR LATE PROMOTER - A NOVEL TRIPARTITE STRUCTURE THAT INCLUDES INTRAGENIC SEQUENCES [J].
AYER, DE ;
DYNAN, WS .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2021-2033
[5]   DNA-SEQUENCE ANALYSIS OF SIMIAN VIRUS-40 MUTANTS WITH DELETIONS MAPPING IN THE LEADER REGION OF THE LATE VIRAL MESSENGER-RNAS - MUTANTS WITH DELETIONS SIMILAR IN SIZE AND POSITION EXHIBIT VARIED PHENOTYPES [J].
BARKAN, A ;
MERTZ, JE .
JOURNAL OF VIROLOGY, 1981, 37 (02) :730-737
[6]   TAT TRANS-ACTIVATES THE HUMAN IMMUNODEFICIENCY VIRUS THROUGH A NASCENT RNA TARGET [J].
BERKHOUT, B ;
SILVERMAN, RH ;
JEANG, KT .
CELL, 1989, 59 (02) :273-282
[7]   CONTROL ELEMENTS SITUATED DOWNSTREAM OF THE MAJOR TRANSCRIPTIONAL START SITE ARE SUFFICIENT FOR HIGHLY EFFICIENT POLYOMAVIRUS LATE TRANSCRIPTION [J].
BOURACHOT, B ;
YANIV, M ;
HERBOMEL, P .
JOURNAL OF VIROLOGY, 1989, 63 (06) :2567-2577
[8]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[9]   STIMULATION OF SIMIAN VIRUS-40 LATE GENE-EXPRESSION BY SIMIAN VIRUS-40 TUMOR-ANTIGEN [J].
BRADY, J ;
BOLEN, JB ;
RADONOVICH, M ;
SALZMAN, N ;
KHOURY, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :2040-2044
[10]   SITE-SPECIFIC BASE SUBSTITUTION AND DELETION MUTATIONS THAT ENHANCE OR SUPPRESS TRANSCRIPTION OF THE SV40 MAJOR LATE RNA [J].
BRADY, J ;
RADONOVICH, M ;
VODKIN, M ;
NATARAJAN, V ;
THOREN, M ;
DAS, G ;
JANIK, J ;
SALZMAN, NP .
CELL, 1982, 31 (03) :625-633