University of Hawaii Cancer Center, Cancer Biology Program, Honolulu, Hawaii 96813, USA.
Department of Oncology-Pathology, Cellular and Molecular Tumor Pathology, Karolinska Institute, and Karolinska University Hospital, Stockholm, 17164 Sweden.
Genome Res. 2019 Sep;29(9):1377-1388. doi: 10.1101/gr.247239.118. Epub 2019 Aug 21.
The world of noncoding RNAs (ncRNAs) is composed of an enormous and growing number of transcripts, ranging in length from tens of bases to tens of kilobases, involved in all biological processes and altered in expression and/or function in many types of human disorders. The premise of this review is the concept that ncRNAs, like many large proteins, have a multidomain architecture that organizes them spatially and functionally. As ncRNAs are beginning to be imprecisely classified into functional families, we review here how their structural properties might inform their functions with focus on structural architecture-function relationships. We will describe the properties of "interactor elements" (IEs) involved in direct physical interaction with nucleic acids, proteins, or lipids and of "structural elements" (SEs) directing their wiring within the "ncRNA interactor networks" through the emergence of secondary and/or tertiary structures. We suggest that spectrums of "letters" (ncRNA elements) are assembled into "words" (ncRNA domains) that are further organized into "phrases" (complete ncRNA structures) with functional meaning (signaling output) through complex "sentences" (the ncRNA interactor networks). This semiotic analogy can guide the exploitation of ncRNAs as new therapeutic targets through the development of IE-blockers and/or SE-lockers that will change the interactor partners' spectrum of proteins, RNAs, DNAs, or lipids and consequently influence disease phenotypes.
非编码 RNA(ncRNA)的世界由大量不断增长的转录本组成,其长度从数十个碱基到数十个千碱基不等,参与所有的生物过程,并在许多类型的人类疾病中表达和/或功能发生改变。本文的前提是这样一个概念,即像许多大型蛋白质一样,ncRNA 具有一种多维结构,这种结构在空间和功能上对其进行组织。由于 ncRNA 开始被不精确地分类为具有功能家族,我们在这里回顾了它们的结构特性如何告知其功能,重点是结构-功能关系。我们将描述涉及与核酸、蛋白质或脂质直接物理相互作用的“相互作用元件”(IE)和指导其在“ncRNA 相互作用网络”中的布线的“结构元件”(SE)的特性,通过二级和/或三级结构的出现。我们认为,“字母”(ncRNA 元件)的频谱被组装成“单词”(ncRNA 结构域),这些结构域通过复杂的“句子”(ncRNA 相互作用网络)进一步组织成具有功能意义(信号输出)的“短语”(完整的 ncRNA 结构)。这种符号学类比可以通过开发 IE 阻断剂和/或 SE 封闭剂来指导 ncRNA 作为新的治疗靶点的开发,这些抑制剂将改变相互作用伴侣的蛋白质、RNA、DNA 或脂质的谱,并因此影响疾病表型。