Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Science. 2013 Aug 16;341(6147):1237973. doi: 10.1126/science.1237973. Epub 2013 Jul 4.
Many large noncoding RNAs (lncRNAs) regulate chromatin, but the mechanisms by which they localize to genomic targets remain unexplored. We investigated the localization mechanisms of the Xist lncRNA during X-chromosome inactivation (XCI), a paradigm of lncRNA-mediated chromatin regulation. During the maintenance of XCI, Xist binds broadly across the X chromosome. During initiation of XCI, Xist initially transfers to distal regions across the X chromosome that are not defined by specific sequences. Instead, Xist identifies these regions by exploiting the three-dimensional conformation of the X chromosome. Xist requires its silencing domain to spread across actively transcribed regions and thereby access the entire chromosome. These findings suggest a model in which Xist coats the X chromosome by searching in three dimensions, modifying chromosome structure, and spreading to newly accessible locations.
许多大型非编码 RNA(lncRNA)调节染色质,但它们定位基因组靶标的机制仍未被探索。我们研究了 Xist lncRNA 在 X 染色体失活(XCI)过程中的定位机制,XCI 是 lncRNA 介导的染色质调节的典范。在 XCI 的维持过程中,Xist 广泛结合在整个 X 染色体上。在 XCI 的起始阶段,Xist 首先转移到 X 染色体上的远端区域,这些区域没有特定的序列定义。相反,Xist 通过利用 X 染色体的三维构象来识别这些区域。Xist 需要其沉默结构域在活跃转录的区域中扩散,从而接触整个染色体。这些发现表明了一个模型,即 Xist 通过在三维空间中搜索、修饰染色体结构并扩散到新的可及位置,从而覆盖整个 X 染色体。