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MiR-144 regulates adipogenesis by mediating formation of C/EBPα-FOXO1 protein complex.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2022 Jul 05; Vol. 612, pp. 126-133. Date of Electronic Publication: 2022 Apr 28. - Publication Year :
- 2022
-
Abstract
- CeRNA effect was an important regulation mode of miRNA mediated bio-activities, however, most of the researches of ceRNA were on ncRNAs synergetic with mRNAs, the exploration of ceRNA effect regulated mRNA interaction was still lack of. Besides, C/EBPα was one of the most crucial adipogenic regulators, which has been demonstrated to form a protein complex with FOXO1 to mediate AdipoQ expression. So that, we try to explore whether the ceRNA effect mediated the interaction of C/EBPα and FOXO1, and identified the key miRNAs of their ceRNA effect. In this paper, we found the ceRNA effect of C/EBPα and FOXO1 mediated their protein complex formation, furthermore regulated its transcriptional role for AdipoQ, thereby influencing pre-adipocytes adipogenesis. More importantly, we demonstrated that the miR-144 was the decisive factor that mediated the ceRNA effect of C/EBPα and FOXO1 to influence AdipoQ, thus regulated pre-adipocytes adipogenesis. This research will provide a new supplementary idea of the miRNA role in mediating coding RNA interaction that regulates pre-adipocyte adipogenesis.<br />Competing Interests: Declaration of competing interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Elsevier Inc. All rights reserved.)
- Subjects :
- 3T3-L1 Cells
Adipocytes metabolism
Animals
CCAAT-Enhancer-Binding Protein-alpha genetics
CCAAT-Enhancer-Binding Protein-alpha metabolism
Cell Differentiation
Forkhead Box Protein O1 genetics
Forkhead Box Protein O1 metabolism
Mice
RNA, Messenger metabolism
Adipogenesis genetics
MicroRNAs metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 612
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 35525196
- Full Text :
- https://doi.org/10.1016/j.bbrc.2022.04.093