Generation of superhelical torsion by ATP-dependent chromatin remodeling activities

被引:212
作者
Havas, K
Flaus, A
Phelan, M
Kingston, R
Wade, PA
Lilley, DMJ
Owen-Hughes, T [1 ]
机构
[1] Univ Dundee, Wellcome Trust Bioctr, Div Gene Regulat, Dundee DD1 5EH, Scotland
[2] Harvard Univ, Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
关键词
D O I
10.1016/S0092-8674(00)00215-4
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
ATP-dependent chromatin remodeling activities participate in the alteration of chromatin structure during gene regulation. Ail have DNA- or chromatin-stimulated ATPase activity and many can alter the structure of chromatin; however, the means by which they do this have remained unclear. Here we describe a novel activity for ATP-dependent chromatin remodeling activities, the ability to generate unconstrained negative superhelical torsion in DNA and chromatin. We find that the ability to distort DNA is shared by the yeast SWI/SNF complex, Xenopus Mi-2 complex, recombinant ISWI, and recombinant BRG1, suggesting that the generation of superhelical torsion represents a primary biomechanical activity shared by all Snf2-prelated ATPase motors. The generation of superhelical torque provides a potent means by which ATP-dependent chromatin remodeling activities can manipulate chromatin structure.
引用
收藏
页码:1133 / 1142
页数:10
相关论文
共 78 条
[1]  
Aasland R, 1996, TRENDS BIOCHEM SCI, V21, P87, DOI 10.1016/0968-0004(96)30009-1
[2]  
Auble DT, 1999, MOL CELL BIOL, V19, P412
[3]  
Bazett-Jones DP, 1999, MOL CELL BIOL, V19, P1470
[4]   DNA in transcriptionally silent chromatin assumes a distinct topology that is sensitive to cell cycle progression [J].
Bi, X ;
Broach, JR .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (12) :7077-7087
[5]   Functional delineation of three groups of the ATP-dependent family of chromatin remodeling enzymes [J].
Boyer, LA ;
Logie, C ;
Bonte, E ;
Becker, PB ;
Wade, PA ;
Wolffe, AP ;
Wu, C ;
Imbalzano, AN ;
Peterson, CL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (25) :18864-18870
[6]   dMi-2 and ISWI chromatin remodelling factors have distinct nucleosome binding and mobilization properties [J].
Brehm, A ;
Längst, G ;
Kehle, J ;
Clapier, CR ;
Imhof, A ;
Eberharter, A ;
Müller, J ;
Becker, PB .
EMBO JOURNAL, 2000, 19 (16) :4332-4341
[7]   RSC, an essential, abundant chromatin-remodeling complex [J].
Cairns, BR ;
Lorch, Y ;
Li, Y ;
Zhang, MC ;
Lacomis, L ;
ErdjumentBromage, H ;
Tempst, P ;
Du, J ;
Laurent, B ;
Kornberg, RD .
CELL, 1996, 87 (07) :1249-1260
[8]   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
[9]   ISWI is an ATP-dependent nucleosome remodeling factor [J].
Corona, DFV ;
Längst, G ;
Clapier, CR ;
Bonte, EJ ;
Ferrari, S ;
Tamkun, JW ;
Becker, PB .
MOLECULAR CELL, 1999, 3 (02) :239-245
[10]   Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle- and developmentally regulated promoter (Publication with Expression of Concern) [J].
Cosma, MP ;
Tanaka, TU ;
Nasmyth, K .
CELL, 1999, 97 (03) :299-311