lncRNA和circRNA在口腔颌面裂中的作用

Ratnam S Seelan, Robert M Greene, M Michele Pisano
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引用次数: 0

摘要

不同的基因调控模式,如组蛋白修饰、转录因子结合、DNA甲基化和微小RNA(miRNA)表达,对基因在发育中的口腔面部组织中的时空表达至关重要。任何一种模式的异常调节都可能导致口腔面部缺陷。非编码RNA(ncRNA),如长ncRNA(lncRNA)和环状RNA(circRNA),已被证明可以改变miRNA的表达,因此正在成为基因调控的新贡献者。其中一些似乎起到了“miRNA海绵”的作用,从而减少了这些miRNA抑制靶基因表达的可用性。这种ncRNA也被称为竞争性内源性RNA(ceRNA)。在这里,我们研究了新出现的数据,这些数据揭示了lncRNA和circRNA如何改变miRNA的调节,从而影响口腔面部发育并可能导致口腔面部分裂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of lncRNAs and circRNAs in Orofacial Clefts.

Different modes of gene regulation, such as histone modification, transcription factor binding, DNA methylation, and microRNA (miRNA) expression, are critical for the spatiotemporal expression of genes in developing orofacial tissues. Aberrant regulation in any of these modes may contribute to orofacial defects. Noncoding RNAs (ncRNAs), such as long ncRNAs (lncRNAs) and circular RNAs (circRNAs), have been shown to alter miRNA expression, and are thus emerging as novel contributors to gene regulation. Some of these appear to function as 'miRNA sponges', thereby diminishing the availability of these miRNAs to inhibit the expression of target genes. Such ncRNAs are also termed competitive endogenous RNAs (ceRNAs). Here, we examine emerging data that shed light on how lncRNAs and circRNAs may alter miRNA regulation, thus affecting orofacial development and potentially contributing to orofacial clefting.

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