| Literature DB >> 19945382 |
Iris Jonkers1, Tahsin Stefan Barakat, Eskeatnaf Mulugeta Achame, Kim Monkhorst, Annegien Kenter, Eveline Rentmeester, Frank Grosveld, J Anton Grootegoed, Joost Gribnau.
Abstract
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.Entities:
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Year: 2009 PMID: 19945382 DOI: 10.1016/j.cell.2009.10.034
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582