Chang Renjie, Zheng Weiwei, Luo Qiang, Liu Guiliang, Xu Tianjun, Sun Yuena
Laboratory of Fish Molecular Immunology, College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China.
Laboratory of Fish Molecular Immunology, College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, China; Laboratory of Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China; Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources (Shanghai Ocean University), Ministry of Education, China; National Pathogen Collection Center for Aquatic Animals, Shanghai Ocean University, China.
Dev Comp Immunol. 2021 Dec;125:104229. doi: 10.1016/j.dci.2021.104229. Epub 2021 Aug 10.
microRNAs (miRNAs), a crucial class of small non-coding RNA species, have been extensively studied as key molecular in immune regulation in the past decades. Here, we discover a new miRNA miR-148-1-5p and we elaborate that miR-148-1-5p functions as a negative regulator to participate in innate immune responses. In this article, it has been researched that the regulation effect of miR-148-1-5p to the nuclear factor kappaB (NF-κB) signaling pathway by targeting IRAK1 in miiuy croaker. First, through bioinformatics software to predict the potential targets of miR-148-1-5p, we found that IRAK1 had a base complementary region with indicated miRNA. Next, the dual-luciferase assays revealed that overexpression of miR-148-1-5p mimics and pre-miR-148 plasmid could significantly inhibit the luciferase activity of wild-type IRAK1-3'UTR. However, miR-148-1-5p inhibitors attenuated the inhibition caused by miR-148-1-5p. In addition, we also confirmed that miR-148-1-5p could suppress the expression of IRAK1 at mRNA level. Collectively, the regulations of miR-148-1-5p to NF-κB signaling pathways via targeting the IRAK1 gene was studied in miiuy croaker, which provided new information to enrich the immune regulation network of miRNA in teleost fish.
微小RNA(miRNA)是一类至关重要的小型非编码RNA,在过去几十年中作为免疫调节的关键分子被广泛研究。在此,我们发现了一种新的miRNA miR-148-1-5p,并阐述了miR-148-1-5p作为负调节因子参与先天免疫反应。在本文中,研究了miR-148-1-5p通过靶向鮸鱼中的白细胞介素-1受体相关激酶1(IRAK1)对核因子κB(NF-κB)信号通路的调节作用。首先,通过生物信息学软件预测miR-148-1-5p的潜在靶标,我们发现IRAK1与所示miRNA有一个碱基互补区域。接下来,双荧光素酶测定显示,miR-148-1-5p模拟物和pre-miR-148质粒的过表达可显著抑制野生型IRAK1-3'UTR的荧光素酶活性。然而,miR-148-1-5p抑制剂减弱了miR-148-1-5p引起的抑制作用。此外,我们还证实miR-148-1-5p可在mRNA水平抑制IRAK1的表达。总的来说,研究了miR-148-1-5p通过靶向IRAK1基因对鮸鱼NF-κB信号通路的调节作用,这为丰富硬骨鱼类miRNA的免疫调节网络提供了新信息。