| Literature DB >> 34105773 |
Lingling Feng1, Yunshan Fan2, Jinjun Zhou1, Shuangshuang Li1, Xiaohua Zhang1.
Abstract
AlkB homolog 5 (ALKBH5) has been reported as a key m6A demethylase that is involved in development and diseases; however, the function of ALKBH5 in osteogenesis remains unknown. In this study, we report that ALKBH5 mRNA and protein expression were upregulated during osteoblast differentiation, and that ALKBH5 knockdown suppressed osteoblast differentiation, mineralization, and the expression of osteogenic biomarkers. Conversely, ALKBH5 overexpression promoted osteogenesis. Moreover, the expression of wild type ALKBH5, but not the m6A-modified active site mutant ALKBH5, could rescue ALKBH5 knockdown-induced osteogenesis inhibition. Furthermore, knockdown of ALKBH5 significantly impaired the mRNA stability of the transcription factor Runx2, which plays a key role in osteoblast differentiation. Taken together, our results suggest that ALKBH5 promotes osteogenesis through modulating Runx2 mRNA stability. This article is protected by copyright. All rights reserved.Entities:
Keywords: ALKBH5; N6-methyladenosine; mRNA stability; osteoblast differentiation
Year: 2021 PMID: 34105773 DOI: 10.1002/1873-3468.14145
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124