The histone macroH2A1.2 has been implicated in X chromosome inactivation on the basis of its accumulation on the inactive X chromosome (Xi) of adult female mammals. We have established the timing of macroH2A1.2 association with the Xi relative to the onset of X-inactivation in differentiating murine embryonic stem (ES) cells using immuno-RNA fluorescence in situ hybridization (FISH). Before X-inactivation we observe a single macroH2A1.2-dense region in both undifferentiated XX and XY ES cells that does not colocalize with X inactive specific transcript (Xist) RNA, and thus appears not to associate with the X chromosome(s). This pattern persists through early stages of differentiation, up to day 7. Then the frequency of XY cells containing a macroH2A1.2-rich domain declines. In contrast, in XX cells there is a striking relocalization of macroH2A1.2 to the Xi. Relocalization occurs in a highly synchronized wave over a 2-d period, indicating a precisely regulated association. The timing of macroH2A1.2 accumulation on the Xi suggests it is not necessary for the initiation or propagation of random X-inactivation.
Skip Nav Destination
Article navigation
27 December 1999
Article|
December 27 1999
Histone Macroh2a1.2 Relocates to the Inactive X Chromosome after Initiation and Propagation of X-Inactivation
Jacqueline E. Mermoud,
Jacqueline E. Mermoud
aX-Inactivation Group, Medical Research Council Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom
Search for other works by this author on:
Carl Costanzi,
Carl Costanzi
bDepartment of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Search for other works by this author on:
John R. Pehrson,
John R. Pehrson
bDepartment of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Search for other works by this author on:
Neil Brockdorff
Neil Brockdorff
aX-Inactivation Group, Medical Research Council Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom
Search for other works by this author on:
Jacqueline E. Mermoud
aX-Inactivation Group, Medical Research Council Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom
Carl Costanzi
bDepartment of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104
John R. Pehrson
bDepartment of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104
Neil Brockdorff
aX-Inactivation Group, Medical Research Council Clinical Sciences Centre, Imperial College School of Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom
Abbreviations used in this paper: DAPI, 4,6-diamidino-2-phenylindole dihydrochloride; EB, embryonic body; ES, embryonic stem; FISH, fluorescence in situ hybridization; LDH, lactate dehydrogenase; LIF, leukemia inhibitory factor; MCB, macrochromatin body; TR, Texas red; Xa, active X chromosome; Xi, inactive X chromosome; Xist, X inactive specific transcript.
Received:
July 16 1999
Revision Requested:
November 02 1999
Accepted:
November 15 1999
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Cell Biol (1999) 147 (7): 1399–1408.
Article history
Received:
July 16 1999
Revision Requested:
November 02 1999
Accepted:
November 15 1999
Citation
Jacqueline E. Mermoud, Carl Costanzi, John R. Pehrson, Neil Brockdorff; Histone Macroh2a1.2 Relocates to the Inactive X Chromosome after Initiation and Propagation of X-Inactivation. J Cell Biol 27 December 1999; 147 (7): 1399–1408. doi: https://doi.org/10.1083/jcb.147.7.1399
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement