The RNA demethylase ALKBH5 promotes osteoblast differentiation by modulating Runx2 mRNA stability

被引:20
|
作者
Feng, Lingling [1 ]
Fan, Yunshan [2 ]
Zhou, Jinjun [1 ]
Li, Shuangshuang [1 ]
Zhang, Xiaohua [1 ]
机构
[1] Nantong Univ, Affiliated Matern & Child Hlth Care Hosp, Dept Paediat, Nantong 226001, Peoples R China
[2] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Orthoped, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
ALKBH5; mRNA stability; N6-methyladenosine; osteoblast differentiation; BONE; OSTEOCYTES; CELLS;
D O I
10.1002/1873-3468.14145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2007 / 2014
页数:8
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