Liu Fei, Somarowthu Srinivas, Pyle Anna Marie
Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut, USA.
Howard Hughes Medical Institute, Chevy Chase, Maryland, USA.
Nat Chem Biol. 2017 Mar;13(3):282-289. doi: 10.1038/nchembio.2272. Epub 2017 Jan 9.
Long noncoding RNAs (lncRNAs) are important for gene expression, but little is known about their structures. RepA is a 1.6-kb mouse lncRNA comprising the same sequence as the 5' region of Xist, including A and F repeats. It has been proposed to facilitate the initiation and spread of X-chromosome inactivation, although its exact role is poorly understood. To gain insight into the molecular mechanism of RepA and Xist, we determined a complete phylogenetically validated secondary-structural map of RepA through SHAPE and DMS chemical probing of a homogeneously folded RNA in vitro. We combined UV-cross-linking experiments with RNA modeling methods to produce a three-dimensional model of RepA functional domains demonstrating that tertiary architecture exists within lncRNA molecules and occurs within specific functional modules. This work provides a foundation for understanding of the evolution and functional properties of RepA and Xist and offers a framework for exploring architectural features of other lncRNAs.
长链非编码RNA(lncRNAs)对基因表达很重要,但对其结构却知之甚少。RepA是一种1.6千碱基的小鼠lncRNA,其序列与Xist的5'区域相同,包括A和F重复序列。虽然其确切作用尚不清楚,但有人提出它有助于X染色体失活的起始和扩散。为了深入了解RepA和Xist的分子机制,我们通过对体外均匀折叠的RNA进行SHAPE和DMS化学探测,确定了RepA完整的、经过系统发育验证的二级结构图谱。我们将紫外线交联实验与RNA建模方法相结合,生成了RepA功能域的三维模型,证明lncRNA分子中存在三级结构,且发生在特定的功能模块内。这项工作为理解RepA和Xist的进化及功能特性奠定了基础,并为探索其他lncRNA的结构特征提供了框架。