Bhartiya Deeksha, Scaria Vinod
GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Mall Road, Delhi 110007, India; Academy of Scientific & Innovative Research (AcSIR), Anusandhan Bhawan, New Delhi 110001, India.
Genomics. 2016 Mar;107(2-3):59-68. doi: 10.1016/j.ygeno.2016.01.005. Epub 2016 Jan 11.
The last decade has seen tremendous improvements in the understanding of human variations and their association with human traits and diseases. The availability of high-resolution map of the human transcriptome and the discovery of a large number of non-protein coding RNA genes has created a paradigm shift in the understanding of functional variations in non-coding RNAs. Several groups in recent years have reported functional variations and trait or disease associated variations mapping to non-coding RNAs including microRNAs, small nucleolar RNAs and long non-coding RNAs. The understanding of the functional consequences of variations in non-coding RNAs has been largely restricted by the limitations in understanding the functionalities of the non-coding RNAs. In this short review, we outline the current state-of-the-art of the field with emphasis on providing a conceptual outline as on how variations could modulate changes in the sequence, structure, and thereby the functionality of non-coding RNAs.
在过去十年中,我们对人类变异及其与人类特征和疾病的关联有了巨大的认识进展。人类转录组高分辨率图谱的出现以及大量非蛋白质编码RNA基因的发现,在对非编码RNA功能变异的理解上引发了范式转变。近年来,多个研究团队报告了与非编码RNA(包括微小RNA、小核仁RNA和长链非编码RNA)相关的功能变异以及与性状或疾病相关的变异。对非编码RNA变异功能后果的理解在很大程度上受到对非编码RNA功能理解的限制。在这篇简短的综述中,我们概述了该领域的当前前沿状况,重点是提供一个概念性概述,说明变异如何调节非编码RNA的序列、结构变化,进而影响其功能。