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
[21]   Characterization of an NF-1/CTF family member as a functional activator of the mouse mammary tumor virus long terminal repeat 5' enhancer [J].
Kusk, P ;
John, S ;
Fragoso, G ;
Michelotti, J ;
Hager, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (49) :31269-31276
[22]   Nucleosome movement by CHRAC and ISWI without disruption or trans-displacement of the histone octamer [J].
Längst, G ;
Bonte, EJ ;
Corona, DFV ;
Becker, PB .
CELL, 1999, 97 (07) :843-852
[23]   2 REGIONS OF THE MOUSE MAMMARY-TUMOR VIRUS LONG TERMINAL REPEAT REGULATE THE ACTIVITY OF ITS PROMOTER IN MAMMARY CELL-LINES [J].
LEFEBVRE, P ;
BERARD, DS ;
CORDINGLEY, MG ;
HAGER, GL .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (05) :2529-2537
[24]   Steroid receptor coactivator-1 (SRC-1) enhances ligand-dependent and receptor-dependent cell-free transcription of chromatin [J].
Liu, Z ;
Wong, JM ;
Tsai, SY ;
Tsai, MJ ;
O'Malley, BW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) :9485-9490
[25]   THE ROLE OF A POSITIONED NUCLEOSOME AT THE DROSOPHILA-MELANOGASTER HSP26 PROMOTER [J].
LU, Q ;
WALLRATH, LL ;
ELGIN, SCR .
EMBO JOURNAL, 1995, 14 (19) :4738-4746
[26]   Crystal structure of the nucleosome core particle at 2.8 angstrom resolution [J].
Luger, K ;
Mader, AW ;
Richmond, RK ;
Sargent, DF ;
Richmond, TJ .
NATURE, 1997, 389 (6648) :251-260
[27]   GENETIC COMPLEMENTATION OF A GLUCOCORTICOID RECEPTOR DEFICIENCY BY EXPRESSION OF CLONED RECEPTOR CDNA [J].
MIESFELD, R ;
RUSCONI, S ;
GODOWSKI, PJ ;
MALER, BA ;
OKRET, S ;
WIKSTROM, AC ;
GUSTAFSSON, JA ;
YAMAMOTO, KR .
CELL, 1986, 46 (03) :389-399
[28]   A HUMAN HOMOLOG OF SACCHAROMYCES-CEREVISIAE SNF2/SWI2 AND DROSOPHILA-BRM GENES POTENTIATES TRANSCRIPTIONAL ACTIVATION BY THE GLUCOCORTICOID RECEPTOR [J].
MUCHARDT, C ;
YANIV, M .
EMBO JOURNAL, 1993, 12 (11) :4279-4290
[29]   SEQUENCE-SPECIFIC INTERACTIONS OF NUCLEAR FACTORS WITH THE INSULIN GENE ENHANCER [J].
OHLSSON, H ;
EDLUND, T .
CELL, 1986, 45 (01) :35-44
[30]   SEQUENCE-SPECIFIC BINDING OF GLUCOCORTICOID RECEPTOR TO MTV DNA AT SITES WITHIN AND UPSTREAM OF THE TRANSCRIBED REGION [J].
PAYVAR, F ;
DEFRANCO, D ;
FIRESTONE, GL ;
EDGAR, B ;
WRANGE, O ;
OKRET, S ;
GUSTAFSSON, JA ;
YAMAMOTO, KR .
CELL, 1983, 35 (02) :381-392