RNF12 Is an X-Encoded Dose-Dependent Activator of X Chromosome Inactivation
Author(s) -
Iris H. Jonkers,
Tahsin Stefan Barakat,
Eskeatnaf Mulugeta,
Kim Monkhorst,
Annegien Kenter,
Eveline Rentmeester,
Frank Grosveld,
J. Anton Grootegoed,
Joost Gribnau
Publication year - 2009
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2009.10.034
Subject(s) - biology , x inactivation , xist , activator (genetics) , somatic cell , x chromosome , embryo , ubiquitin ligase , microbiology and biotechnology , transgene , genetics , open reading frame , skewed x inactivation , gene , ubiquitin , peptide sequence
In somatic cells of female placental mammals, one X chromosome is inactivated to minimize sex-related dosage differences of X-encoded genes. Random X chromosome inactivation (XCI) in the embryo is a stochastic process, in which each X has an independent probability to initiate XCI, triggered by the nuclear concentration of one or more X-encoded XCI-activators. Here, we identify the E3 ubiquitin ligase RNF12 as an important XCI-activator. Additional copies of mouse Rnf12 or human RNF12 result in initiation of XCI in male mouse ES cells and on both X chromosomes in a substantial percentage of female mouse ES cells. This activity is dependent on an intact open reading frame of Rnf12 and correlates with the transgenic expression level of RNF12. Initiation of XCI is markedly reduced in differentiating female heterozygous Rnf12(+/-) ES cells. These findings provide evidence for a dose-dependent role of RNF12 in the XCI counting and initiation process.
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