Myc influences global chromatin structure.
Journal: 2006/August - EMBO Journal
ISSN: 0261-4189
Abstract:
The family of myc proto-oncogenes encodes transcription factors (c-, N-, and L-Myc) that regulate cell growth and proliferation and are involved in the etiology of diverse cancers. Myc proteins are thought to function by binding and regulating specific target genes. Here we report that Myc proteins are required for the widespread maintenance of active chromatin. Disruption of N-myc in neuronal progenitors and other cell types leads to nuclear condensation accompanied by large-scale changes in histone modifications associated with chromatin inactivation, including hypoacetylation and altered methylation. These effects are largely reversed by exogenous Myc as well as by differentiation and are mimicked by the Myc antagonist Mad1. The first chromatin changes are evident within 6 h of Myc loss and lead to changes in chromatin structure. Myc widely influences chromatin in part through upregulation of the histone acetyltransferase GCN5. This study provides the first evidence for regulation of global chromatin structure by an oncoprotein and may explain the broad effects of Myc on cell behavior and tumorigenesis.
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EMBO J 25(12): 2723-2734

Myc influences global chromatin structure

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
The Wistar Institute, Gene Expression and Regulation Program, Philadelphia, PA, USA
Proteomics Facility, Fred Hutchinson Cancer Research Center, Seattle, WA, USA
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N, Seattle, WA 98109-4417, USA. Tel.: +1 206 667 4445; Fax: +1 206 667 6522; E-mail: gro.crchf@namnesie
Received 2005 Dec 6; Accepted 2006 Apr 27.

Abstract

The family of myc proto-oncogenes encodes transcription factors (c-, N-, and L-Myc) that regulate cell growth and proliferation and are involved in the etiology of diverse cancers. Myc proteins are thought to function by binding and regulating specific target genes. Here we report that Myc proteins are required for the widespread maintenance of active chromatin. Disruption of N-myc in neuronal progenitors and other cell types leads to nuclear condensation accompanied by large-scale changes in histone modifications associated with chromatin inactivation, including hypoacetylation and altered methylation. These effects are largely reversed by exogenous Myc as well as by differentiation and are mimicked by the Myc antagonist Mad1. The first chromatin changes are evident within 6 h of Myc loss and lead to changes in chromatin structure. Myc widely influences chromatin in part through upregulation of the histone acetyltransferase GCN5. This study provides the first evidence for regulation of global chromatin structure by an oncoprotein and may explain the broad effects of Myc on cell behavior and tumorigenesis.

Keywords: chromatin, epigenetics, histone modification, Myc, stem and progenitor cells
Abstract
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Acknowledgments

We thank Ignacio Moreno de Alboran for the c-myc flox/flox mice, Tina Xu for excellent technical assistance, Anna Kenney and David Rowitch for teaching us CGNP culture and for reagents, Amir Orian for sharing unpublished data, John Sedivy and Yuzuru Shiio for the c-myc null rat fibroblasts, and Bobbie Schneider and the FHCRC EM staff for excellent technical help. We are indebted to Samir Hanash for access to the LTQ-FT and to Hong Wang and Doug Phanstiel for collection of the mass spectrometry data. We also thank Steve Henikoff, Mark Groudine, Susan Mendrysa, Julie Secombe, and Amir Orian for critical reading of the manuscript. We also thank Santa Cruz Biotechnology for help with antibodies. The authors have no competing interests. This work was supported by NIH/NCI grant CA20525 to RNE and KOICA114400-01 to PSK. RNE is an American Cancer Society Professor.

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