Human Molecular Genetics Advance Access originally published online on July 15, 2003
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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
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
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
J. Ausio Histone variants--the structure behind the function Brief Funct Genomic Proteomic, September 1, 2006; 5(3): 228 - 243. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||







