A transient heterochromatic state in Xist preempts X inactivation choice without RNA stabilization

被引:241
|
作者
Sun, BK
Deaton, AM
Lee, JT [1 ]
机构
[1] Massachusetts Gen Hosp, Howard Hughes Med Inst, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.molcel.2006.01.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X chromosome inactivation (XCI) depends on a non-coding sense-antisense transcript pair, Xist and Tsix. At the onset of XCI, Xist RNA accumulates on one of two Xs, coating and silencing the chromosome in cis. The molecular basis for monoallelic Xistupregulation is not known, though evidence predominantly supports a posttranscriptional mechanism through RNA stabilization. Here, we test whether Tsix RNA destabilizes Xist RNA. Unexpectedly, we find that Xistupregulation is not based on transcript stabilization at all but is instead controlled by transcription in a sex-specif ic manner. Tsix directly regulates its transcription. On the future inactive X, Tsix downregulation induces a transient heterochromatic state in Xist, followed paradoxically by high-level Xist expression. A Tsix-deficient X chromosome adopts the heterochromatic state in pre-XCI cells. This state persists through XCI establishment and "reverts" to a euchromatic state during XCI maintenance. We have therefore identified chromatin marks that preempt and predict asymmetric Xist expression.
引用
收藏
页码:617 / 628
页数:12
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