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

Author:

Bourgo Ryan J.1,Siddiqui Hasan2,Fox Sejal3,Solomon David4,Sansam Courtney G.5,Yaniv Moshe6,Muchardt Christian6,Metzger Daniel7,Chambon Pierre7,Roberts Charles W.M.5,Knudsen Erik S.1

Affiliation:

1. *Department of Cancer Biology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107;

2. Human Cancer Genetics Program, Department of Molecular Virology, Immunology, and Medical Genetics, Comprehensive Cancer Center, College of Medicine and Public Health, The Ohio State University, Columbus, OH 43210;

3. Department of Cell and Cancer Biology, University of Cincinnati College of Medicine, Cincinnati, OH 45267;

4. Lombardi Comprehensive Cancer Center, Georgetown University School of Medicine, Washington, DC, 20057;

5. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115

6. Expression Génétique et Maladies, Formation de Recherche en Evolution 2850 du Centre National de la Recherche Scientifique, Département de Biologie du Développement, Institut Pasteur, 75724 Paris, France;

7. Institut de Génétique et Biologie Moléculaire et Cellulaire, Department of Functional Genomics, F-67400 Illkirch, France; Institut National de la Santé et de la Recherche Médicale, U596, F-67400 Illkirch, France; Centre National de la Recherche Scientifique, Unité Mixte de Recherche 7104, F-67400 Illkirch, France; Université Louis Pasteur, F-67000 Strasbourg, France; Collége de France, F-67400 Illkirch, France; and

Abstract

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.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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