Institute of Genomics, School of Medicine, Huaqiao University, 668 Jimei Road, Xiamen, 361021, China.
AcademGene Ltd., 6, Acad. Lavrentjev ave, Novosibirsk, 630090, Russia.
BMC Biol. 2021 May 20;19(1):108. doi: 10.1186/s12915-021-01044-x.
The majority of the human genome is transcribed in the form of long non-coding (lnc) RNAs. While these transcripts have attracted considerable interest, their molecular mechanisms of function and biological significance remain controversial. One of the main reasons behind this lies in the significant challenges posed by lncRNAs requiring the development of novel methods and concepts to unravel their functionality. Existing methods often lack cross-validation and independent confirmation by different methodologies and therefore leave significant ambiguity as to the authenticity of the outcomes. Nonetheless, despite all the caveats, it appears that lncRNAs may function, at least in part, by regulating other genes via chromatin interactions. Therefore, the function of a lncRNA could be inferred from the function of genes it regulates. In this work, we present a genome-wide functional annotation strategy for lncRNAs based on identification of their regulatory networks via the integration of three distinct types of approaches: co-expression analysis, mapping of lncRNA-chromatin interactions, and assaying molecular effects of lncRNA knockdowns obtained using an inducible and highly specific CRISPR/Cas13 system.
We applied the strategy to annotate 407 very long intergenic non-coding (vlinc) RNAs belonging to a novel widespread subclass of lncRNAs. We show that vlincRNAs indeed appear to regulate multiple genes encoding proteins predominantly involved in RNA- and development-related functions, cell cycle, and cellular adhesion via a mechanism involving proximity between vlincRNAs and their targets in the nucleus. A typical vlincRNAs can be both a positive and negative regulator and regulate multiple genes both in trans and cis. Finally, we show vlincRNAs and their regulatory networks potentially represent novel components of DNA damage response and are functionally important for the ability of cancer cells to survive genotoxic stress.
This study provides strong evidence for the regulatory role of the vlincRNA class of lncRNAs and a potentially important role played by these transcripts in the hidden layer of RNA-based regulation in complex biological systems.
人类基因组的大部分以长非编码 RNA(lncRNA)的形式转录。虽然这些转录物引起了相当大的兴趣,但它们的功能分子机制和生物学意义仍然存在争议。其中一个主要原因在于,lncRNA 存在很大的挑战,需要开发新的方法和概念来揭示它们的功能。现有的方法往往缺乏不同方法的交叉验证和独立确认,因此对于结果的真实性仍然存在很大的不确定性。尽管存在所有这些警告,但似乎 lncRNA 至少可以通过染色质相互作用来调节其他基因。因此,可以根据其调节的基因的功能来推断 lncRNA 的功能。在这项工作中,我们提出了一种基于通过整合三种不同类型的方法来识别其调节网络的全基因组 lncRNA 功能注释策略:共表达分析、lncRNA-染色质相互作用的映射以及使用诱导和高度特异性的 CRISPR/Cas13 系统获得的 lncRNA 敲低的分子效应测定。
我们应用该策略对属于新型广泛的 lncRNA 亚类的 407 个非常长的基因间非编码 RNA(vlincRNA)进行了注释。我们表明,vlincRNA 确实似乎通过涉及 vlincRNA 与其在核中的靶标之间的接近性的机制来调节编码主要涉及 RNA 和发育相关功能、细胞周期和细胞粘附的蛋白质的多个基因。典型的 vlincRNA 既可以是正调节因子,也可以是负调节因子,可以在转和反式调节多个基因。最后,我们表明 vlincRNA 及其调节网络可能代表 DNA 损伤反应的新组成部分,并且对于癌细胞在遗传毒性应激下存活的能力具有重要的功能。
这项研究为 vlincRNA 类 lncRNA 的调节作用提供了强有力的证据,并为这些转录物在复杂生物系统中基于 RNA 的调节的隐藏层中发挥的潜在重要作用提供了证据。