Department of Urology, University of California, San Francisco, San Francisco, CA, USA.
San Francisco Veterans Affairs Medical Center, San Francisco, CA, USA.
Cell Mol Life Sci. 2018 Feb;75(3):467-484. doi: 10.1007/s00018-017-2626-6. Epub 2017 Aug 24.
Non-coding RNA (ncRNA) has been shown to regulate diverse cellular processes and functions through controlling gene expression. Long non-coding RNAs (lncRNAs) act as a competing endogenous RNAs (ceRNAs) where microRNAs (miRNAs) and lncRNAs regulate each other through their biding sites. Interactions of miRNAs and lncRNAs have been reported to trigger decay of the targeted lncRNAs and have important roles in target gene regulation. These interactions form complicated and intertwined networks. Certain lncRNAs encode miRNAs and small nucleolar RNAs (snoRNAs), and may regulate expression of these small RNAs as precursors. SnoRNAs have also been reported to be precursors for PIWI-interacting RNAs (piRNAs) and thus may regulate the piRNAs as a precursor. These miRNAs and piRNAs target messenger RNAs (mRNAs) and regulate gene expression. In this review, we will present and discuss these interactions, cross-talk, and co-regulation of ncRNAs and gene regulation due to these interactions.
非编码 RNA(ncRNA)已被证明通过控制基因表达来调节多种细胞过程和功能。长非编码 RNA(lncRNA)作为竞争性内源 RNA(ceRNA)起作用,其中 microRNA(miRNA)和 lncRNA 通过结合位点相互调节。已经报道了 miRNA 和 lncRNA 的相互作用会触发靶向 lncRNA 的降解,并在靶基因调节中发挥重要作用。这些相互作用形成复杂且相互交织的网络。某些 lncRNA 编码 miRNA 和小核仁 RNA(snoRNA),并可能作为前体调节这些小 RNA 的表达。snoRNA 也被报道为 PIWI 相互作用 RNA(piRNA)的前体,因此可能作为前体调节 piRNA。这些 miRNA 和 piRNA 靶向信使 RNA(mRNA)并调节基因表达。在这篇综述中,我们将介绍和讨论这些相互作用、ncRNA 的串扰和协同调节以及由于这些相互作用导致的基因调节。