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The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development
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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194157/ https://www.ncbi.nlm.nih.gov/pubmed/14676303 http://dx.doi.org/10.1084/jem.20030714 |
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author | Gebuhr, Thomas C. Kovalev, Grigoriy I. Bultman, Scott Godfrey, Virginia Su, Lishan Magnuson, Terry |
author_facet | Gebuhr, Thomas C. Kovalev, Grigoriy I. Bultman, Scott Godfrey, Virginia Su, Lishan Magnuson, Terry |
author_sort | Gebuhr, Thomas C. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2194157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21941572008-04-11 The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development Gebuhr, Thomas C. Kovalev, Grigoriy I. Bultman, Scott Godfrey, Virginia Su, Lishan Magnuson, Terry J Exp Med Article 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. The Rockefeller University Press 2003-12-15 /pmc/articles/PMC2194157/ /pubmed/14676303 http://dx.doi.org/10.1084/jem.20030714 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Gebuhr, Thomas C. Kovalev, Grigoriy I. Bultman, Scott Godfrey, Virginia Su, Lishan Magnuson, Terry The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development |
title | The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development |
title_full | The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development |
title_fullStr | The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development |
title_full_unstemmed | The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development |
title_short | The Role of Brg1, a Catalytic Subunit of Mammalian Chromatin-remodeling Complexes, in T Cell Development |
title_sort | role of brg1, a catalytic subunit of mammalian chromatin-remodeling complexes, in t cell development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194157/ https://www.ncbi.nlm.nih.gov/pubmed/14676303 http://dx.doi.org/10.1084/jem.20030714 |
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