Abstract
MicroRNAs (miRNAs) are endogenously expressed small noncoding RNAs and play critical roles in the regulation of post-transcriptional gene expression. Our previous study uncovered that chi-miR-487b-3p is widespread in different goat tissues, which is significantly higher in muscle, especially in lamb. Here, we demonstrate the role of chi-miR-487b-3p as a myogenic miRNA that regulates skeletal muscle development. chi-miR-487b-3p overexpression was demonstrated to significantly inhibit goat myoblast proliferation and differentiation, whereas chi-miR-487b-3p inhibition resulted in the opposite effects. Next, chi-miR-487b-3p was predicted to target the 3′UTR of insulin receptor substrate 1 (IRS1) gene by Target-Scan and miRDB. The results of dual-luciferase assay, RT-qPCR, and western blot all confirmed that IRS1 might be a direct target of chi-miR-487b-3p as its expression was negatively regulated by chi-miR-487b-3p. siRNA silencing of IRS1 further demonstrated significant inhibition on goat myoblast proliferation and differentiation, confirming the effect of IRS1 downregulation by chi-miR-487b-3p in myogenesis. In addition, chi-miR-487b-3p knockout goat myoblast clones were generated using CRISPR/Cas9 technology, and we further illustrated that chi-miR-487b-3p regulates goat myoblast growth through the PI3K/Akt signaling pathway by targeting IRS1. Collectively, our work demonstrated that chi-miR-487b-3p is a potent inhibitor of skeletal myogenesis and provided new insights into the mechanisms of miRNA on the regulation of goat growth.
Highlights
Skeletal muscle is the most abundant tissue in mammals and plays an important role in body metabolism [1]
We further examined the role of insulin receptor substrate 1 (IRS1) during goat myoblast proliferation and differentiation by RNA interference
Compared with the siNC control, siIRS1 decreased the expression of differentiation genes (MyoG and myosin heavy chain (MyHC)) at both the messenger RNAs (mRNAs) and protein levels (Figure 5K–M). These results indicate that IRS1 silencing represses goat myoblast proliferation and differentiation
Summary
Skeletal muscle is the most abundant tissue in mammals and plays an important role in body metabolism [1]. During the formation of skeletal muscle, mononucleated myoblasts expand, migrate, and differentiate into myoblasts, which is a complex process regulated by a group of myogenic regulatory factors (MRF). All these factors including myogenic factor 5 (Myf5), myogenic determination 1 (MyoD1), myogenin (MyoG), and myosin heavy chain (MyHC) are the key regulators of skeletal muscle development [2,3]. The short single-stranded miRNA binds to the 30 untranslated region (30 UTR) of the specific mRNA based on sequence homology, resulting in the degradation of target mRNA or repression of corresponding protein translation [6,7]
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