Center for Dynamic Personal Regulomes, Stanford University, Stanford, CA 94305, USA.
Center for Dynamic Personal Regulomes, Stanford University, Stanford, CA 94305, USA
Philos Trans R Soc Lond B Biol Sci. 2017 Nov 5;372(1733). doi: 10.1098/rstb.2016.0356.
X-chromosome inactivation (XCI) is a critical epigenetic mechanism for balancing gene dosage between XY males and XX females in eutherian mammals. A long non-coding RNA (lncRNA), XIST, and its associated proteins orchestrate this multi-step process, resulting in the inheritable silencing of one of the two X-chromosomes in females. The XIST RNA is large and complex, exemplifying the unique challenges associated with the structural and functional analysis of lncRNAs. Recent technological advances in the analysis of macromolecular structure and interactions have enabled us to systematically dissect the XIST ribonucleoprotein complex, which is larger than the ribosome, and its place of action, the inactive X-chromosome. These studies shed light on key mechanisms of XCI, such as XIST coating of the X-chromosome, recruitment of DNA, RNA and histone modification enzymes, and compaction and compartmentalization of the inactive X. Here, we summarize recent studies on XCI, highlight the critical contributions of new technologies and propose a unifying model for XIST function in XCI where modular domains serve as the structural and functional units in both lncRNA-protein complexes and DNA-protein complexes in chromatin.This article is part of the themed issue 'X-chromosome inactivation: a tribute to Mary Lyon'.
X 染色体失活(XCI)是真哺乳类动物中 XY 雄性和 XX 雌性之间平衡基因剂量的关键表观遗传机制。长非编码 RNA(lncRNA)XIST 及其相关蛋白协调这一多步过程,导致女性两条 X 染色体中的一条可遗传沉默。XIST RNA 很大且复杂,体现了 lncRNA 结构和功能分析所特有的挑战。最近在分析大分子结构和相互作用方面的技术进步使我们能够系统地剖析 XIST 核糖核蛋白复合物,该复合物大于核糖体,以及其作用的场所,即失活 X 染色体。这些研究揭示了 XCI 的关键机制,例如 XIST 对 X 染色体的包被、DNA、RNA 和组蛋白修饰酶的募集,以及失活 X 的压缩和区室化。在这里,我们总结了最近关于 XCI 的研究,强调了新技术的关键贡献,并提出了一个统一的模型,用于 XIST 在 XCI 中的功能,其中模块化结构域作为 lncRNA-蛋白复合物和染色质中 DNA-蛋白复合物的结构和功能单位。本文是主题为“X 染色体失活:向玛丽·莱昂致敬”的特刊的一部分。