Circular PPP1R13B RNA Promotes Chicken Skeletal Muscle Satellite Cell Proliferation and Differentiation via Targeting miR-9-5p.
Xiaoxu ShenYuanhang WeiGuishuang YouWei LiuFelix Kwame AmevorYao ZhangHaorong HeMenggen MaYun ZhangDiyan LiQing ZhuHuadong YinPublished in: Animals : an open access journal from MDPI (2021)
Skeletal muscle plays important roles in animal locomotion, metabolism, and meat production in farm animals. Current studies showed that non-coding RNAs, especially the circular RNA (circRNA) play an indispensable role in skeletal muscle development. Our previous study revealed that several differentially expressed circRNAs among fast muscle growing broilers (FMGB) and slow muscle growing layers (SMGL) may regulate muscle development in the chicken. In this study, a novel differentially expressed circPPP1R13B was identified. Molecular mechanism analysis indicated that circPPP1R13B targets miR-9-5p and negatively regulates the expression of miR-9-5p, which was previously reported to be an inhibitor of skeletal muscle development. In addition, circPPP1R13B positively regulated the expression of miR-9-5p target gene insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3) and further activated the downstream insulin like growth factors (IGF)/phosphatidylinositol 3-kinase (PI3K)/AKT serine/threonine kinase (AKT) signaling pathway. The results also showed that the knockdown of circPPP1R13B inhibits chicken skeletal muscle satellite cells (SMSCs) proliferation and differentiation, and the overexpression of circPPP1R13B promotes the proliferation and differentiation of chicken SMSCs. Furthermore, the overexpression of circPPP1R13B could block the inhibitory effect of miR-9-5p on chicken SMSC proliferation and differentiation. In summary, our results suggested that circPPP1R13B promotes chicken SMSC proliferation and differentiation by targeting miR-9-5p and activating IGF/PI3K/AKT signaling pathway.
Keyphrases
- pi k akt
- signaling pathway
- skeletal muscle
- cell cycle arrest
- induced apoptosis
- cell proliferation
- binding protein
- insulin resistance
- epithelial mesenchymal transition
- protein kinase
- poor prognosis
- transcription factor
- type diabetes
- tyrosine kinase
- metabolic syndrome
- cell cycle
- genome wide
- dna methylation
- cell death
- heat stress
- weight loss
- data analysis
- case control