COOPERATIVE BENDING OF THE 21-BASE-PAIR REPEATS OF THE SV40 VIRAL EARLY PROMOTER BY HUMAN SP1

被引:30
作者
SUN, D
HURLEY, LH
机构
[1] Drug Dynamics Institute, College of Pharmacy, University of Texas at Austin, Austin
关键词
D O I
10.1021/bi00198a025
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
The overall structural features of the multimeric complex between Sp1 and the 21-base-pair repeat of the early promoter region of SV40 DNA have been determined using hydroxyl-radical footprinting; (+)-CC-1065, a sequence-specific minor groove bending probe; and circularization experiments. The results show that the 21-base-pair repeat region has an intrinsically in-phase bent structure that is stabilized upon saturation Sp1 binding by protein-DNA and protein-protein interactions to produce a looping structure. The direction of the Sp1-stabilized bending of DNA occurs into the minor groove and is localized between each of the Sp1 binding sites. These results are used as the basis to propose a looping structure for the multimeric Sp1 21-base-pair repeat region of SV40 DNA. Last, these results provide a rationale for the recently observed inhibition of basal transcriptional levels by site-specific triple-helical DNA complexes.
引用
收藏
页码:9578 / 9587
页数:10
相关论文
共 53 条
[1]   EXPRESSION OF A BETA-GLOBIN GENE IS ENHANCED BY REMOTE SV40 DNA-SEQUENCES [J].
BANERJI, J ;
RUSCONI, S ;
SCHAFFNER, W .
CELL, 1981, 27 (02) :299-308
[2]   STRUCTURAL DETAILS OF AN ADENINE TRACT THAT DOES NOT CAUSE DNA TO BEND [J].
BURKHOFF, AM ;
TULLIUS, TD .
NATURE, 1988, 331 (6155) :455-457
[3]   MODE OF INTERACTION OF THE ZINC FINGER PROTEIN TFIIIA WITH A 5S RNA GENE OF XENOPUS [J].
CHURCHILL, MEA ;
TULLIUS, TD ;
KLUG, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5528-5532
[4]   SYNERGISTIC ACTIVATION BY THE GLUTAMINE-RICH DOMAINS OF HUMAN TRANSCRIPTION FACTOR SP1 [J].
COUREY, AJ ;
HOLTZMAN, DA ;
JACKSON, SP ;
TJIAN, R .
CELL, 1989, 59 (05) :827-836
[5]   ANALYSIS OF SP1 INVIVO REVEALS MULTIPLE TRANSCRIPTIONAL DOMAINS, INCLUDING A NOVEL GLUTAMINE-RICH ACTIVATION MOTIF [J].
COUREY, AJ ;
TJIAN, R .
CELL, 1988, 55 (05) :887-898
[6]   (+)-CC-1065 AS A STRUCTURAL PROBE OF MU TRANSPOSASE-INDUCED BENDING OF DNA - OVERCOMING LIMITATIONS OF HYDROXYL-RADICAL FOOTPRINTING [J].
DING, ZM ;
HARSHEY, RM ;
HURLEY, LH .
NUCLEIC ACIDS RESEARCH, 1993, 21 (18) :4281-4287
[7]   DISTAMYCIN-INDUCED INHIBITION OF HOMEODOMAIN DNA COMPLEXES [J].
DORN, A ;
AFFOLTER, M ;
MULLER, M ;
GEHRING, WJ ;
LEUPIN, W .
EMBO JOURNAL, 1992, 11 (01) :279-286
[8]   THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR-SP1 BINDS TO UPSTREAM SEQUENCES IN THE SV40 EARLY PROMOTER [J].
DYNAN, WS ;
TJIAN, R .
CELL, 1983, 35 (01) :79-87
[9]   TRANSCRIPTION FACTOR SP1 RECOGNIZES PROMOTER SEQUENCES FROM THE MONKEY GENOME THAT ARE SIMILAR TO THE SIMIAN VIRUS-40 PROMOTER [J].
DYNAN, WS ;
SAFFER, JD ;
LEE, WS ;
TJIAN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (15) :4915-4919
[10]   THE REPEATED GC-RICH MOTIFS UPSTREAM FROM THE TATA BOX ARE IMPORTANT ELEMENTS OF THE SV40 EARLY PROMOTER [J].
EVERETT, RD ;
BATY, D ;
CHAMBON, P .
NUCLEIC ACIDS RESEARCH, 1983, 11 (08) :2447-2464