circRNA对细胞复杂调控网络的影响

L. Porta, A. Caterina
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引用次数: 1

摘要

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。
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Impact of circRNA on the complex regulatory network of the cell
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.
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