Glucocorticoid receptor-glucocorticoid response element binding stimulates nucleosome disruption by the SWI/SNF complex

被引:137
作者
Farrants, AKO
Blomquist, P
Kwon, H
Wrange, O
机构
[1] KAROLINSKA INST, MED NOBEL INST, DEPT CELL & MOL BIOL, S-17177 STOCKHOLM, SWEDEN
[2] DANKOOK UNIV, DEPT BIOL MOL, SEOUL 140714, SOUTH KOREA
关键词
D O I
10.1128/MCB.17.2.895
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 organization of DNA in chromatin is involved in repressing basal transcription of a number of inducible genes, Biochemically defined multiprotein complexes such as SWI/SNF (J. Cote, J. Quinn, J. L. Workman, and C. L. Peterson, Science 265:53-60, 1994) and nucleosome remodeling factor (T. Tsukiyama and C. Wu, Cell 83:1011-1020, 1995) disrupt nucleosomes in vitro and are thus candidates for complexes which cause chromatin decondensation during gene induction, In this study we show that the glucocorticoid receptor (GR), a hormone-inducible transcription factor, stimulates the nucleosome-disrupting activity of the SWI/SNF complex partially purified either from HeLa cells or from rat liver tissue, This GR-mediated stimulation of SWI/SNF nucleosome disruption depended on the presence of a glucocorticoid response element, The in vitro-reconstituted nucleosome probes used in these experiments harbored 95 bp of synthetic DNA-bending sequence in order to rotationally position the DNA, The GR-dependent stimulation of SWI/SNF-mediated nucleosome disruption, as evaluated by DNase I footprinting, was 2.7- to 3.8-fold for the human SWI/SNF complex and 2.5 to 3.2-fold for the rat SWI/SNF complex, When nuclear factor 1 (NF1) was used instead of GR, there was no stimulation of SWI/SNF activity in the presence of a mononucleosome containing an NF1 binding site, On the other hand, the SWI/SNF nucleosome disruption activity increased the access of NF1 for its nucleosomal binding site. No such effect was seen on binding of GR to its response element, Our results suggest that GR, but not NF1, is able to target the nucleosome-disrupting activity of the SWI/SNF complex.
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收藏
页码:895 / 905
页数:11
相关论文
共 68 条
[1]   NUCLEOSOME DISPLACEMENT IN TRANSCRIPTION [J].
ADAMS, CC ;
WORKMAN, JL .
CELL, 1993, 72 (03) :305-308
[2]   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
[3]   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
[4]   The affinity of nuclear factor 1 for its DNA site is drastically reduced by nucleosome organization irrespective of its rotational or translational position [J].
Blomquist, P ;
Li, Q ;
Wrange, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (01) :153-159
[5]   Evidence that Spt6p controls chromatin structure by a direct interaction with histones [J].
Bortvin, A ;
Winston, F .
SCIENCE, 1996, 272 (5267) :1473-1476
[6]  
BRENOWITZ M, 1986, METHOD ENZYMOL, V130, P132
[7]   A MULTISUBUNIT COMPLEX CONTAINING THE SWI1/ADR6, SWI2/SNF2, SWI3, SNF5, AND SNF6 GENE-PRODUCTS ISOLATED FROM YEAST [J].
CAIRNS, BR ;
KIM, YJ ;
SAYRE, MH ;
LAURENT, BC ;
KORNBERG, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (05) :1950-1954
[8]   THE SNF/SWI FAMILY OF GLOBAL TRANSCRIPTIONAL ACTIVATORS [J].
CARLSON, M ;
LAURENT, BC .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (03) :396-402
[9]   GLUCOCORTICOIDS LOCALLY DISRUPT AN ARRAY OF POSITIONED NUCLEOSOMES ON THE RAT TYROSINE AMINOTRANSFERASE PROMOTER IN HEPATOMA-CELLS [J].
CARR, KD ;
RICHARDFOY, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9300-9304
[10]   2 HUMAN HOMOLOGS OF SACCHAROMYCES-CEREVISIAE SW12/SNF2 AND DROSOPHILA-BRAHMA ARE TRANSCRIPTIONAL COACTIVATORS COOPERATING WITH THE ESTROGEN-RECEPTOR AND THE RETINOIC ACID RECEPTOR [J].
CHIBA, H ;
MURAMATSU, M ;
NOMOTO, A ;
KATO, H .
NUCLEIC ACIDS RESEARCH, 1994, 22 (10) :1815-1820