Mammalian SWI–SNF-related complexes use brahma-related gene 1 (Brg1) as a catalytic subunit to remodel nucleosomes and regulate transcription. Recent biochemical data has linked Brg1 function to genes important for T lymphocyte differentiation. To investigate the role of SWI–SNF-related complexes in this lineage, we ablated Brg1 function in T lymphocytes. T cell–specific Brg1-deficient mice showed profound thymic abnormalities, CD4 derepression at the double negative (DN; CD4− CD8−) stage, and a developmental block at the DN to double positive (CD4+ CD8+) transition. 5′-bromo-2′-deoxyuridine incorporation and annexin V staining establish a role for Brg1 complexes in the regulation of thymocyte cell proliferation and survival. This Brg1-dependent cell survival is specific for developing thymocytes as indicated by the presence of Brg1-deficient mature T lymphocytes that have escaped the developmental block in the thymus. However, reductions in peripheral T cell populations lead to immunodeficiency and compromised health of mutant mice. These results highlight the importance of chromatin-remodeling complexes at different stages in the development of a mammalian cell lineage.
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15 December 2003
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December 15 2003
The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development
Thomas C. Gebuhr,
Thomas C. Gebuhr
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Grigoriy I. Kovalev,
Grigoriy I. Kovalev
2Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Scott Bultman,
Scott Bultman
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Virginia Godfrey,
Virginia Godfrey
3Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Lishan Su,
Lishan Su
2Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Terry Magnuson
Terry Magnuson
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
5Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
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Thomas C. Gebuhr
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Grigoriy I. Kovalev
2Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Scott Bultman
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Virginia Godfrey
3Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Lishan Su
2Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Terry Magnuson
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
4Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
5Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Address correspondence to Terry Magnuson, Department of Genetics, Neurosciences Research Building, Room 4109D, University of North Carolina, CB 7264, 103 Mason Farm Road, Chapel Hill, NC 27599. Phone: (919) 843-6475; Fax: (919) 843-6365; email: [email protected]
T.C. Gebuhr and G.I. Kovalev contributed equally to this work.
The online version of this article contains supplemental material.
Abbreviations used in this paper: BrdU, 5′-bromo-2′-deoxyuridine; Brg1, brahma-related gene 1; Brm, brahma; DN, double negative; DP, double positive; PI, propidium iodide; SP, single positive; TN, triple negative.
Received:
May 01 2003
Accepted:
November 04 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2003
J Exp Med (2003) 198 (12): 1937–1949.
Article history
Received:
May 01 2003
Accepted:
November 04 2003
Citation
Thomas C. Gebuhr, Grigoriy I. Kovalev, Scott Bultman, Virginia Godfrey, Lishan Su, Terry Magnuson; The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development . J Exp Med 15 December 2003; 198 (12): 1937–1949. doi: https://doi.org/10.1084/jem.20030714
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