4.4 Article

Effect of miR-493-5p on proliferation and differentiation of myoblast by targeting ANKRD17

Journal

CELL AND TISSUE RESEARCH
Volume 393, Issue 1, Pages 119-132

Publisher

SPRINGER
DOI: 10.1007/s00441-023-03777-3

Keywords

MiRNA; Muscle; C2C12; miR-493-5p; RNA-seq

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The hypertrophy and conversion of postnatal muscle fibers are crucial for determining the yield and quality of meat in pigs. This study used miRNA-seq to profile the longissimus dorsi tissues of Lantang pigs at 1 and 90 days, identifying differentially expressed miRNAs and exploring the role of miR-493-5p in myogenesis. The results suggest that miR-493-5p promotes myoblast proliferation and inhibits differentiation, and it is associated with muscle development by targeting ANKRD17 gene.
The hypertrophy and conversion of postnatal muscle fibers largely determine the yield and quality of meat, which is closely related to the economic value of pigs. MicroRNA (miRNA), as a kind of endogenous noncoding RNA molecule, is widely involved in myogenesis of livestock and poultry. The longissimus dorsi tissues of Lantang pigs at 1 and 90 days (LT1D and LT90D) were collected and profiled by miRNA-seq. We found 1871 and 1729 miRNA candidates in LT1D and LT90D samples, and 794 miRNAs were shared. We identified 16 differentially expressed miRNAs between two tested groups and explored the function of miR-493-5p inmyogenesis. The miR-493-5p promoted the proliferation and inhibited the differentiation of myoblasts. Using GO and KEGG analyses of 164 target genes of miR-493-5p, we found that ATP2A2, PPP3CA, KLF15, MED28, and ANKRD17 genes were related to muscle development. RT-qPCR detection showed that the expression level of ANKRD17 was highly expressed in LT1D libraries, and the double luciferase report test preliminarily proved that miR-493-5p and ANKRD17 have a directly targeting relationship. We established miRNA profiles for the longissimus dorsi tissues of 1-day-old and 90-day-old Lantang pigs and found that miR-493-5p was differentially expressed and associated with myogenesis by targeting ANKRD17 gene. Our results should serve as a reference for future studies on pork quality.

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