SWI/SNF Deficiency Results in Aberrant Chromatin Organization, Mitotic Failure, and Diminished Proliferative Capacity

被引:56
作者
Bourgo, Ryan J. [1 ]
Siddiqui, Hasan [2 ]
Fox, Sejal [3 ]
Solomon, David [4 ]
Sansam, Courtney G. [11 ]
Yaniv, Moshe [5 ]
Muchardt, Christian [5 ]
Metzger, Daniel [6 ,7 ,8 ,9 ,10 ]
Chambon, Pierre [6 ,7 ,8 ,9 ,10 ]
Roberts, Charles W. M. [11 ]
Knudsen, Erik S. [1 ]
机构
[1] Thomas Jefferson Univ, Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA
[2] Ohio State Univ, Coll Med & Publ Hlth, Ctr Comprehens Canc, Human Canc Genet Program,Dept Mol Virol Immunol &, Columbus, OH 43210 USA
[3] Univ Cincinnati, Coll Med, Dept Cell & Canc Biol, Cincinnati, OH 45267 USA
[4] Georgetown Univ, Sch Med, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[5] Inst Pasteur, Dept Dev Biol, CNRS, F-75724 Paris, France
[6] Inst Genet & Biol Mol & Cellulaire, Dept Funct Genom, F-67400 Illkirch Graffenstaden, France
[7] INSERM, U596, F-67400 Illkirch Graffenstaden, France
[8] CNRS, UMR 7104, F-67400 Illkirch Graffenstaden, France
[9] Univ Strasbourg, F-67000 Strasbourg, France
[10] Coll France, F-67400 Illkirch Graffenstaden, France
[11] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
关键词
REMODELING COMPLEX; CHROMOSOME SEGREGATION; BRG1; BRM; HAPLOINSUFFICIENCY; HETEROCHROMATIN; REPRESSION; MUTATIONS; PROTEIN; CANCER;
D O I
10.1091/mbc.E08-12-1224
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Switch (SWI)/sucrose nonfermentable (SNF) is an evolutionarily conserved complex with ATPase function, capable of regulating nucleosome position to alter transcriptional programs within the cell. It is known that the SWI/SNF complex is responsible for regulation of many genes involved in cell cycle control and proliferation, and it has recently been implicated in cancer development. The ATPase action of SWI/SNF is conferred through either the brahma-related gene 1 (Brg1) or brahma (Brm) subunit of the complex, and it is of central importance to the modification of nucleosome position. In this study, the role of the Brg1 and Brm subunits were examined as they relate to chromatin structure and organization. Deletion of the Brg1 ATPase results in dissolution of pericentromeric heterochromatin domains and a redistribution of histone modifications associated with these structures. This effect was highly specific to Brg1 and is not reproduced by the loss of Brm or SNF5/BAF47/INI1. Brg1 deficiency is associated with the appearance of micronuclei and aberrant mitoses that are a by-product of dissociated chromatin structure. Thus, Brg1 plays a critical role in maintaining chromatin structural integrity.
引用
收藏
页码:3192 / 3199
页数:8
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