Arnott Malcolm, Sampilo Nina Faye, Song Jia L
Department of Biological Sciences, University of Delaware, Newark, DE, United States.
Front Cell Dev Biol. 2024 Apr 24;12:1356589. doi: 10.3389/fcell.2024.1356589. eCollection 2024.
In early embryonic development, the cross-regulation of transcription factors and signaling pathways are critical in mediating developmental and physiological processes. Additionally, many studies have shown the importance of post-transcriptional regulation of signaling and network components mediated by microRNAs (miRNAs); however, how miRNAs are transcriptionally regulated is poorly understood. miRNAs are critical fine-tuners of many biological processes and their dysregulation leads to a variety of diseases and developmental defects. Previously, we have shown that miRNAs are dynamically expressed throughout sea urchin development, suggesting that miRNAs are likely to be under transcriptional regulation. Here, we used pharmacological inhibitors, genetic constructs, and loss-of-function reagents to assess the impact of key signaling pathways (Wnt, Nodal, MAPK, Sonic Hedgehog, Delta/Notch, VEGF, and BMP) and transcription factors (Alx1, Ets1/2, and Tbr) on the transcript levels of the evolutionarily conserved miR-1, miR-31, miR-92 and miR-124; the invertebrate-specific miR-71; and the echinoderm-specific miR-2002, miR-2007, and miR-2012. We also used computational methods to identify potential transcription factor binding sites of these miRNAs. Lists of binding motifs for transcription factors (TFs) were acquired from the MEME-Suite Motif Database and used as inputs for the algorithm FIMO (Find Individual Motif Occurrences), which detects short nucleotide motifs within larger sequences. Based on experimental data on miRNA expression in conjunction with bioinformatic predictions, we propose that the transcription factors Tbr, Alx1, and Ets1 regulate miR-1, miR-31, and miR-71, respectively. We additionally observed significant effects on miRNA levels as a result of perturbations to Wnt, Nodal, MAPK, and Sonic Hedgehog signaling pathways, while no significant change on miRNA levels were observed with perturbations to Delta/Notch, VEGF, or BMP signaling pathways. Overall, this study provides insights into the transcriptional regulation of miRNAs by signaling pathways and transcription factors and contribute to our overall understanding of the genetic regulation of developmental processes.
在早期胚胎发育过程中,转录因子和信号通路的交叉调控对于介导发育和生理过程至关重要。此外,许多研究表明,微小RNA(miRNA)介导的信号和网络组件的转录后调控具有重要意义;然而,miRNA的转录调控方式却鲜为人知。miRNA是许多生物学过程的关键微调因子,其失调会导致多种疾病和发育缺陷。此前,我们已经表明miRNA在海胆发育过程中动态表达,这表明miRNA可能受到转录调控。在这里,我们使用药理学抑制剂、基因构建体和功能丧失试剂来评估关键信号通路(Wnt、Nodal、MAPK、Sonic Hedgehog、Delta/Notch、VEGF和BMP)和转录因子(Alx1、Ets1/2和Tbr)对进化保守的miR-1、miR-31、miR-92和miR-124;无脊椎动物特异性miR-71;以及棘皮动物特异性miR-2002、miR-2007和miR-2012转录水平的影响。我们还使用计算方法来识别这些miRNA潜在的转录因子结合位点。从MEME-Suite基序数据库获取转录因子(TF)的结合基序列表,并将其用作算法FIMO(查找单个基序出现情况)的输入,该算法可检测较大序列中的短核苷酸基序。基于miRNA表达的实验数据以及生物信息学预测,我们提出转录因子Tbr、Alx1和Ets1分别调控miR-1、miR-31和miR-71。我们还观察到,Wnt、Nodal、MAPK和Sonic Hedgehog信号通路的扰动对miRNA水平有显著影响,而Delta/Notch、VEGF或BMP信号通路的扰动对miRNA水平没有显著变化。总体而言,本研究深入探讨了信号通路和转录因子对miRNA的转录调控,有助于我们全面理解发育过程的遗传调控。