Skip Navigation


Human Molecular Genetics Advance Access originally published online on July 15, 2003
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
12/17/2167    most recent
ddg229v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (40)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Chadwick, B. P.
Right arrow Articles by Willard, H. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chadwick, B. P.
Right arrow Articles by Willard, H. F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2003, Vol. 12, No. 17 2167-2178
DOI: 10.1093/hmg/ddg229
© 2003 Oxford University Press

Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome

Brian P. Chadwick and Huntington F. Willard*

Institute for Genome Sciences and Policy and Department of Molecular Genetics and Microbiology, Duke University, Durham, NC 27710, USA

Received November 20, 2003; Revised May 2, 2003; Accepted July 1, 2003

The Barr body has long been recognized as the cytological manifestation of the inactive X chromosome (Xi) in interphase nuclei. Despite being known for over 50 years, relatively few components of the Barr body have been identified. In this study, we have screened over 30 histone variants, modified histones and non-histone proteins for their association with or exclusion from the Barr body. We demonstrate that, similar to the histone variant macroH2A, heterochromatin protein-1 (HP1), histone H1 and the high mobility group protein HMG-I/Y are elevated at the territory of the Xi in interphase in human cell lines, but only when the Xi chromatin is heteropycnotic, implicating each as a component of the Barr body. Surprisingly, however, virtually all other candidate proteins involved in establishing heterochromatin and gene silencing are notably absent from the Barr body despite being localized generally elsewhere throughout the nucleus, indicating that the Barr body represents a discrete subnuclear compartment that is not freely accessible to most chromatin proteins. A similar dichotomous pattern of association or exclusion describes the spatial relationship of a number of specific histone methylation patterns in relation to the Barr body. Notably, though, several methylated forms of histone H3 that are deficient in Xi chromatin generally are present at a region near the macrosatellite repeat DXZ4, as are the chromatin proteins CTCF and SAP30, indicating a distinctive chromatin state in this region of the Xi. Taken together, our data imply that the Xi adopts a distinct chromatin configuration in interphase nuclei and are consistent with a mechanism by which HP1, through histone H3 lysine-9 methylation, recognizes and assists in maintaining heterochromatin and gene silencing at the human Xi.

* To whom correspondence should be addressed at: Institute for Genome Sciences and Policy, Duke University, Box 3382, Durham, NC 27710, USA. Tel: +1 9196684477; Fax: +1 9196680795; Email: hunt.willard{at}duke.edu


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
JCBHome page
L. L. Hall, M. Byron, G. Pageau, and J. B. Lawrence
AURKB-mediated effects on chromatin regulate binding versus release of XIST RNA to the inactive chromosome
J. Cell Biol., August 24, 2009; 186(4): 491 - 507.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
B. P. Chadwick
DXZ4 chromatin adopts an opposing conformation to that of the surrounding chromosome and acquires a novel inactive X-specific role involving CTCF and antisense transcripts
Genome Res., August 1, 2008; 18(8): 1259 - 1269.
[Abstract] [Full Text] [PDF]


Home page
Brief Funct Genomic ProteomicHome page
M. A. Osley
Regulation of histone H2A and H2B ubiquitylation
Brief Funct Genomic Proteomic, September 1, 2006; 5(3): 179 - 189.
[Abstract] [Full Text] [PDF]


Home page
Brief Funct Genomic ProteomicHome page
J. Ausio
Histone variants--the structure behind the function
Brief Funct Genomic Proteomic, September 1, 2006; 5(3): 228 - 243.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J. Chaumeil, P. Le Baccon, A. Wutz, and E. Heard
A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced.
Genes & Dev., August 15, 2006; 20(16): 2223 - 2237.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
Y. Costa, R. M. Speed, P. Gautier, C. A. Semple, K. Maratou, J. M.A. Turner, and H. J. Cooke
Mouse MAELSTROM: the link between meiotic silencing of unsynapsed chromatin and microRNA pathway?
Hum. Mol. Genet., August 1, 2006; 15(15): 2324 - 2334.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
J. H. Choo, J. D. Kim, J. H. Chung, L. Stubbs, and J. Kim
Allele-specific deposition of macroH2A1 in imprinting control regions
Hum. Mol. Genet., March 1, 2006; 15(5): 717 - 724.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. W. Abbott, B. P. Chadwick, A. A. Thambirajah, and J. Ausio
Beyond the Xi: MacroH2A CHROMATIN DISTRIBUTION AND POST-TRANSLATIONAL MODIFICATION IN AN AVIAN SYSTEM
J. Biol. Chem., April 22, 2005; 280(16): 16437 - 16445.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
B. P. Chadwick and H. F. Willard
Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome
PNAS, December 14, 2004; 101(50): 17450 - 17455.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
S. A. Grigoryev, T. Nikitina, J. R. Pehrson, P. B. Singh, and C. L. Woodcock
Dynamic relocation of epigenetic chromatin markers reveals an active role of constitutive heterochromatin in the transition from proliferation to quiescence
J. Cell Sci., December 1, 2004; 117(25): 6153 - 6162.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
K. L. Arney and A. G. Fisher
Epigenetic aspects of differentiation
J. Cell Sci., September 1, 2004; 117(19): 4355 - 4363.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
L. Schmiedeberg, K. Weisshart, S. Diekmann, G. Meyer zu Hoerste, and P. Hemmerich
High- and Low-mobility Populations of HP1 in Heterochromatin of Mammalian Cells
Mol. Biol. Cell, June 1, 2004; 15(6): 2819 - 2833.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
N. Kourmouli, P. Jeppesen, S. Mahadevhaiah, P. Burgoyne, R. Wu, D. M. Gilbert, S. Bongiorni, G. Prantera, L. Fanti, S. Pimpinelli, et al.
Heterochromatin and tri-methylated lysine 20 of histone H4 in animals
J. Cell Sci., May 15, 2004; 117(12): 2491 - 2501.
[Abstract] [Full Text] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
E. HEARD, J. CHAUMEIL, O. MASUI, and I. OKAMOTO
Mammalian X-Chromosome Inactivation: An Epigenetics Paradigm
Cold Spring Harb Symp Quant Biol, January 1, 2004; 69(0): 89 - 102.
[Abstract] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
M. LACHNER, R. SENGUPTA, G. SCHOTTA, and T. JENUWEIN
Trilogies of Histone Lysine Methylation as Epigenetic Landmarks of the Eukaryotic Genome
Cold Spring Harb Symp Quant Biol, January 1, 2004; 69(0): 209 - 218.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
S. A. Grigoryev, T. Nikitina, J. R. Pehrson, P. B. Singh, and C. L. Woodcock
Dynamic relocation of epigenetic chromatin markers reveals an active role of constitutive heterochromatin in the transition from proliferation to quiescence
J. Cell Sci., December 1, 2004; 117(25): 6153 - 6162.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.