Department of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul 06591, South Korea; Catholic Institute for Visual Science, College of Medicine, The Catholic University of Korea, Seoul 06591, South Korea.
Department of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul 06591, South Korea.
Biochem Biophys Res Commun. 2020 Jan 22;521(4):971-976. doi: 10.1016/j.bbrc.2019.11.030. Epub 2019 Nov 10.
RNA binding protein HuD regulates translation and turnover of target mRNAs, thereby affecting gene expression at the posttranscriptional level in mainly neuronal as well as pancreatic β-cells. Here, we identified insulinoma-associated 1 (INSM1), an essential factor governing differentiation and proliferation of neuroendocrine cells, as a novel target of HuD and demonstrated the regulatory mechanism of INSM1 expression by HuD. HuD bound to 3'untranslated region (3'UTR) of Insm1 mRNA and negatively regulated its expression; knockdown of HuD increased INSM1 expression, while HuD overexpression repressed it by destabilizing its mRNA. In addition, we further demonstrated that HuD enhanced reduction of INSM1 by miR-203a, a novel miRNA targeting Insm1 mRNA 3'UTR. These results suggest that HuD and miR-203a cooperatively regulate INSM1 expression and it provides a novel regulatory mechanism of INSM1 expression by HuD and miR-203a.
RNA 结合蛋白 HuD 调节靶 mRNA 的翻译和周转,从而在主要神经元和胰腺β细胞中影响转录后水平的基因表达。在这里,我们鉴定出胰岛素瘤相关 1(INSM1),一种调节神经内分泌细胞分化和增殖的必需因子,是 HuD 的一个新靶标,并证明了 HuD 对 INSM1 表达的调节机制。HuD 结合到 Insm1 mRNA 的 3'非翻译区(3'UTR)并负调控其表达;HuD 的敲低增加了 INSM1 的表达,而 HuD 的过表达通过使其 mRNA 不稳定来抑制其表达。此外,我们进一步证明 HuD 增强了 miR-203a 对 INSM1 的减少,miR-203a 是一种靶向 Insm1 mRNA 3'UTR 的新型 miRNA。这些结果表明 HuD 和 miR-203a 协同调节 INSM1 的表达,为 HuD 和 miR-203a 对 INSM1 表达的调节提供了一种新的机制。