Abdelmohsen Kotb, Panda Amaresh C, Munk Rachel, Grammatikakis Ioannis, Dudekula Dawood B, De Supriyo, Kim Jiyoung, Noh Ji Heon, Kim Kyoung Mi, Martindale Jennifer L, Gorospe Myriam
a Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health , Baltimore , MD , USA.
RNA Biol. 2017 Mar 4;14(3):361-369. doi: 10.1080/15476286.2017.1279788. Epub 2017 Jan 12.
HuR influences gene expression programs and hence cellular phenotypes by binding to hundreds of coding and noncoding linear RNAs. However, whether HuR binds to circular RNAs (circRNAs) and impacts on their function is unknown. Here, we have identified en masse circRNAs binding HuR in human cervical carcinoma HeLa cells. One of the most prominent HuR target circRNAs was hsa_circ_0031288, renamed CircPABPN1 as it arises from the PABPN1 pre-mRNA. Further analysis revealed that HuR did not influence CircPABPN1 abundance; interestingly, however, high levels of CircPABPN1 suppressed HuR binding to PABPN1 mRNA. Evaluation of PABPN1 mRNA polysomes indicated that PABPN1 translation was modulated positively by HuR and hence negatively by CircPABPN1. We propose that the extensive binding of CircPABPN1 to HuR prevents HuR binding to PABPN1 mRNA and lowers PABPN1 translation, providing the first example of competition between a circRNA and its cognate mRNA for an RBP that affects translation.
HuR通过与数百种编码和非编码线性RNA结合来影响基因表达程序,进而影响细胞表型。然而,HuR是否与环状RNA(circRNA)结合并影响其功能尚不清楚。在这里,我们在人宫颈癌HeLa细胞中大规模鉴定了与HuR结合的circRNA。最显著的HuR靶标circRNA之一是hsa_circ_0031288,因其来源于PABPN1前体mRNA而重新命名为CircPABPN1。进一步分析表明,HuR不影响CircPABPN1的丰度;然而,有趣的是,高水平的CircPABPN1抑制HuR与PABPN1 mRNA的结合。对PABPN1 mRNA多核糖体的评估表明,PABPN1的翻译受到HuR的正向调节,因此受到CircPABPN1的负向调节。我们提出,CircPABPN1与HuR的广泛结合会阻止HuR与PABPN1 mRNA的结合,并降低PABPN1的翻译,这为circRNA与其同源mRNA之间竞争影响翻译的RNA结合蛋白提供了首个实例。