Affiliation:
1. Department of Molecular Biology, Massachusetts General Hospital; Department of Genetics, Harvard Medical School; and Howard Hughes Medical Institute, Boston, MA 02114, USA.
Abstract
In mammals, dosage compensation is achieved by X-chromosome inactivation (XCI) in the female. The noncoding
Xist
gene initiates silencing of the X chromosome, whereas its antisense partner
Tsix
blocks silencing. The complementarity of Xist and Tsix RNAs has long suggested a role for RNA interference (RNAi). Here, we report that murine Xist and Tsix form duplexes in vivo. During XCI, the duplexes are processed to small RNAs (sRNAs), most likely on the active X (Xa) in a Dicer-dependent manner. Deleting
Dicer
compromises sRNA production and derepresses
Xist.
Furthermore, without Dicer, Xist RNA cannot accumulate and histone 3 lysine 27 trimethylation is blocked on the inactive X (Xi). The defects are partially rescued by truncating Tsix. Thus, XCI and RNAi intersect, down-regulating
Xist
on Xa and spreading silencing on Xi.
Publisher
American Association for the Advancement of Science (AAAS)
Cited by
246 articles.
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