Porcine Circular RNA Insulin-like Growth Factor 1 Receptor Promotes Adipocyte Differentiation
10.13865/j.cnki.cjbmb.2022.02.1554
- Author:
Na ZHANG
1
;
Meng LI
1
;
Jiao LI
1
;
Shan MENG
1
;
Chun-Bo CAI
1
;
Yang YANG
1
;
Peng-Fei GAO
1
;
Xiao-Hong GUO
1
;
Guo-Qing CAO
1
;
Bu-Gao LI
1
Author Information
1. College of Animal Sciences, Shanxi Agricultural University
- Publication Type:Journal Article
- Keywords:
adipogenic differentiation;
circular RNA (circRNA);
competing endogenous RNAs (ceRNA);
insulin-like growthfactor 1 receptor (IGF1R);
mesenchymal stem cells C3H10T1 / 2
- From:
Chinese Journal of Biochemistry and Molecular Biology
2022;38(3):333-342
- CountryChina
- Language:Chinese
-
Abstract:
Circular RNA (circRNA), as a competitive endogenous RNA (ceRNA), plays an importantrole in the regulation of cell differentiation. The purpose of this study was to identify and analyze porcinecircular RNA insulin-like growth factor 1 receptor (circIGF1R), explore its expression patterns, construct a ceRNA regulatory network related to circIGF1R, and explore the regulation of its ectopicexpression on adipogenic differentiation of mouse mesenchymal stem cells (C3H10T1 / 2) effect. Forwardand reverse PCR, Sanger sequencing, RNase R enzyme digestion tests, and qRT-PCR were used toverify that circIGF1R is a circRNA formed by the second exon of insulin-like growth factor 1 receptor(IGF1R). It was expressed in all tissues of pigs, and its expression level increased with age in adiposetissues. miRDB, TargetScan and miRWalk online software were used to predict circIGF1R target genes. RNAhybrid software was used for binding site prediction. DAVID bioinformatics functional analysissoftware was used to perform GO and KEGG enrichment analysis on candidate target genes. Cytoscapesoftware was used to construct the ceRNA network diagram. Based on the gene expression correlation andpredicted target relationship, the GO and KEGG enrichment analysis was drawn and the ceRNA networkwas constructed; the dual luciferase reporter gene test was used, and we found that circIGF1R andFABP4 can bind to ssc (Sus scrofa chromosome) -miR-133a-5p. The circIGF1R overexpression vectorwas successfully constructed and expressed in C3H10T1/ 2 cells. It was found that after overexpression ofcircIGF1R, the expression of key adipogenic regulatory factors CEBPa, CEBPß, FABP4 and PPAR? increased significantly(P<0. 01), and the number of lipid droplets increased significantly. The results ofthis study show that circIGF1R exists in pig adipose tissues, and may positively regulate the adipogenicdifferentiation of C3H10T1/ 2 cells through the ceRNA mechanism, which lays a theoretical foundation forfurther research on circIGF1R regulating the adipogenic differentiation of pig precursor intramuscularadipocytes.
