Nachtigall Pedro G, Dias Marcos C, Carvalho Robson F, Martins Cesar, Pinhal Danillo
Department of Genetics, Institute of Biosciences, Sao Paulo State University (UNESP), Botucatu, Sao Paulo, 18618-970, Brazil.
Department of Morphology, Institute of Biosciences, Sao Paulo State University (UNESP), Botucatu, Sao Paulo, 18618-970, Brazil; Health Sciences Institute, Federal University of Mato Grosso (UFMT), Sinop, Mato Grosso, 78550-000, Brazil.
PLoS One. 2015 Mar 20;10(3):e0119804. doi: 10.1371/journal.pone.0119804. eCollection 2015.
A class of small non-coding RNAs, the microRNAs (miRNAs), has been shown to be essential for the regulation of specific cell pathways, including skeletal muscle development, maintenance and homeostasis in vertebrates. However, the relative contribution of miRNAs for determining the red and white muscle cell phenotypes is far from being fully comprehended. To better characterize the role of miRNA in skeletal muscle cell biology, we investigated muscle-specific miRNA (myomiR) signatures in Nile tilapia fish. Quantitative (RT-qPCR) and spatial (FISH) expression analyses revealed a highly differential expression (forty-four-fold) of miR-499 in red skeletal muscle compared to white skeletal muscle, whereas the remaining known myomiRs were equally expressed in both muscle cell types. Detailed examination of the miR-499 targets through bioinformatics led us to the sox6 and rod1 genes, which had low expression in red muscle cells according to RT-qPCR, FISH, and protein immunofluorescence profiling experiments. Interestingly, we verified that the high expression of miR-499 perfectly correlates with a low expression of sox6 and rod1 target genes, as verified by a distinctive predominance of mRNA destabilization and protein translational decay to these genes, respectively. Through a genome-wide comparative analysis of SOX6 and ROD1 protein domains and through an in silico gene regulatory network, we also demonstrate that both proteins are essentially similar in vertebrate genomes, suggesting their gene regulatory network may also be widely conserved. Overall, our data shed light on the potential regulation of targets by miR-499 associated with the slow-twitch muscle fiber type phenotype. Additionally the results provide novel insights into the evolutionary dynamics of miRNA and target genes enrolled in a putative constrained molecular pathway in the skeletal muscle cells of vertebrates.
一类小的非编码RNA,即微小RNA(miRNA),已被证明对特定细胞途径的调节至关重要,包括脊椎动物的骨骼肌发育、维持和体内平衡。然而,miRNA在决定红肌和白肌细胞表型方面的相对作用远未得到充分理解。为了更好地表征miRNA在骨骼肌细胞生物学中的作用,我们研究了尼罗罗非鱼中肌肉特异性miRNA(肌miR)特征。定量(RT-qPCR)和空间(FISH)表达分析显示,与白色骨骼肌相比,红色骨骼肌中miR-499的表达差异很大(44倍),而其余已知的肌miR在两种肌肉细胞类型中表达相同。通过生物信息学对miR-499靶标的详细研究,我们发现了sox6和rod1基因,根据RT-qPCR、FISH和蛋白质免疫荧光分析实验,这两个基因在红色肌细胞中的表达较低。有趣的是,我们证实miR-499的高表达与sox6和rod1靶基因的低表达完美相关,分别通过对这些基因的mRNA去稳定化和蛋白质翻译衰减的显著优势得到验证。通过对SOX6和ROD1蛋白结构域的全基因组比较分析以及通过计算机基因调控网络,我们还证明这两种蛋白在脊椎动物基因组中基本相似,表明它们的基因调控网络也可能广泛保守。总体而言,我们的数据揭示了与慢肌纤维类型表型相关的miR-499对靶标的潜在调控。此外,这些结果为参与脊椎动物骨骼肌细胞中假定的受限分子途径的miRNA和靶基因的进化动力学提供了新的见解。