Impact of circRNA on the complex regulatory network of the cell

L. Porta, A. Caterina
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引用次数: 1

Abstract

MicroRNAs (miRNAs) are small nucleotides that can bind to messenger RNA (mRNA) preventing its translation. Different mRNA targets can have the same miRNA binding site leading to a miRNA-mediated cross-talk between competitive endogenous RNA (ceRNA) species (1-3). Circular RNAs (circRNAs) are yet another example of ceRNAs (4), first discovered by electron microscopy in an RNA virus in 1976 (5). These are single stranded non-coding RNAs that have their 3' and 5' ends covalently linked due to back-splicing, thus acquiring a circular form. Due to their low transcript abundance, circRNAs were originally thought to be a byproduct of aberrant splicing of mRNA (6). In recent years, however, progress in high-throughput technologies and bioinformatics lead to the identification of many new circRNAs.
circRNA对细胞复杂调控网络的影响
微小核糖核酸(miRNA)是一种小核苷酸,可以与信使核糖核酸(mRNA)结合,阻止其翻译。不同的mRNA靶标可以具有相同的miRNA结合位点,从而导致竞争性内源性RNA(ceRNA)物种之间的miRNA介导的串扰(1-3)。环状RNA(circRNA)是ceRNA的又一个例子(4),1976年首次通过电子显微镜在RNA病毒中发现(5)。这些是单链非编码RNA,其3'和5'端由于反向剪接而共价连接,从而获得圆形形式。由于其转录物丰度低,circRNA最初被认为是mRNA异常剪接的副产品(6)。然而,近年来,高通量技术和生物信息学的进步导致了许多新的circRNA的鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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