Hormone activation induces nucleosome positioning in vivo

被引:55
作者
Belikov, S
Gelius, B
Almouzni, G
Wrange, Ö
机构
[1] Karolinska Inst, Med Nobel Inst, Dept Cell & Mol Biol, Mol Genet Lab, SE-17177 Stockholm, Sweden
[2] Russian Acad Sci, VA Engelhardt Mol Biol Inst, Moscow 117984, Russia
[3] Inst Curie, UMR 218 CNRS, FR-75231 Paris 05, France
关键词
chromatin structure; glucocorticoid receptor; MMTV promoter; nucleosome positioning; Xenopus oocyte;
D O I
10.1093/emboj/19.5.1023
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 mouse mammary tumor virus (MMTV) promoter is induced by glucocorticoid hormone. A robust hormone- and receptor-dependent activation could be reproduced in Xenopus laevis oocytes. The homogeneous response in this system allowed a detailed analysis of the transition in chromatin structure following hormone activation. This revealed two novel findings: hormone activation led to the establishment of specific translational positioning of nucleosomes despite the lack of significant positioning in the inactive state; and, in the active promoter, a subnucleosomal particle encompassing the glucocorticoid receptor (GR)-binding region was detected. The presence of only a single GR-binding site was sufficient for the structural transition to occur, Both basal promoter elements and ongoing transcription were dispensable. These data reveal a stepwise process in the transcriptional activation by glucocorticoid hormone.
引用
收藏
页码:1023 / 1033
页数:11
相关论文
共 54 条
[1]   REPLICATION-COUPLED CHROMATIN ASSEMBLY IS REQUIRED FOR THE REPRESSION OF BASAL TRANSCRIPTION IN-VIVO [J].
ALMOUZNI, G ;
WOLFFE, AP .
GENES & DEVELOPMENT, 1993, 7 (10) :2033-2047
[2]   TRANSCRIPTION FACTOR ACCESS IS MEDIATED BY ACCURATELY POSITIONED NUCLEOSOMES ON THE MOUSE MAMMARY-TUMOR VIRUS PROMOTER [J].
ARCHER, TK ;
CORDINGLEY, MG ;
WOLFORD, RG ;
HAGER, GL .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :688-698
[3]   TRANSCRIPTION FACTOR LOADING ON THE MMTV PROMOTER - A BIMODAL MECHANISM FOR PROMOTER ACTIVATION [J].
ARCHER, TK ;
LEFEBVRE, P ;
WOLFORD, RG ;
HAGER, GL .
SCIENCE, 1992, 255 (5051) :1573-1576
[4]   THE TRANSCRIPTIONALLY-ACTIVE MMTV PROMOTER IS DEPLETED OF HISTONE H1 [J].
BRESNICK, EH ;
BUSTIN, M ;
MARSAUD, V ;
RICHARDFOY, H ;
HAGER, GL .
NUCLEIC ACIDS RESEARCH, 1992, 20 (02) :273-278
[5]   DISTINCT SEQUENCE ELEMENTS INVOLVED IN THE GLUCOCORTICOID REGULATION OF THE MOUSE MAMMARY-TUMOR VIRUS PROMOTER IDENTIFIED BY LINKER SCANNING MUTAGENESIS [J].
BUETTI, E ;
KUHNEL, B .
JOURNAL OF MOLECULAR BIOLOGY, 1986, 190 (03) :379-389
[6]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[7]  
Colman A, 1984, TRANSCRIPTION TRANSL, P49
[8]   STEROID-DEPENDENT INTERACTION OF TRANSCRIPTION FACTORS WITH THE INDUCIBLE PROMOTER OF MOUSE MAMMARY-TUMOR VIRUS INVIVO [J].
CORDINGLEY, MG ;
RIEGEL, AT ;
HAGER, GL .
CELL, 1987, 48 (02) :261-270
[9]   Two-step synergism between the progesterone receptor and the DNA-binding domain of nuclear factor 1 on MMTV minichromosomes [J].
Di Croce, L ;
Koop, R ;
Venditti, P ;
Westphal, HM ;
Nightingale, KP ;
Corona, DFV ;
Becker, PB ;
Beato, M .
MOLECULAR CELL, 1999, 4 (01) :45-54
[10]   Glucocorticoid receptor-glucocorticoid response element binding stimulates nucleosome disruption by the SWI/SNF complex [J].
Farrants, AKO ;
Blomquist, P ;
Kwon, H ;
Wrange, O .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (02) :895-905