E3 ligase Deltex2 accelerates myoblast proliferation and inhibits myoblast differentiation by targeting Pax7 and MyoD, respectively

被引:0
作者
Zhu, Qi [1 ]
Liang, Ziyun [1 ]
Cai, Shufang [1 ]
Tong, Xian [1 ]
Wang, Xiaoyu [1 ]
Li, Enru [1 ]
Chen, Yaosheng [1 ]
Mo, Delin [1 ]
机构
[1] Sun Yat Sen Univ, Sch Life Sci, State Key Lab Biocontrol, Guangzhou 510260, Peoples R China
来源
ACTA BIOCHIMICA ET BIOPHYSICA SINICA | 2023年 / 55卷 / 02期
基金
中国国家自然科学基金;
关键词
E3 ubiquitin ligases; Deltex2; myoblast proliferation and differentiation; Pax7; MyoD; SKELETAL-MUSCLE; SATELLITE CELLS; MYOGENIC CELLS; NOTCH; ACTIVATION; GENES; REGENERATION; PROGRESSION; POPULATION; SUPPRESSOR;
D O I
10.3724/abbs.2023025
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
E3 ubiquitin ligases are closely related to cell division, differentiation, and survival in all eukaryotes and play crucial regulatory roles in multiple biological processes and diseases. While Deltex2, as a member of the DELTEX family ubiquitin ligases, is characterized by a RING domain followed by a C-terminal domain (DTC), its functions and underlying mechanisms in myogenesis have not been fully elucidated. Here, we report that Deltex2, which is highly expressed in muscles, positively regulates myoblast proliferation via mediating the expression of Pax7. Meanwhile, we find that Deltex2 is translocated from the nucleus into the cytoplasm during myogenic differentiation, and further disclose that Deltex2 inhibits myoblast differentiation and interacts with MyoD, resulting in the ubiquitination and degradation of MyoD. Altogether, our findings reveal the physiological function of Deltex2 in orchestrating myogenesis and delineate the novel role of Deltex2 as a negative regulator of MyoD protein stability.
引用
收藏
页码:250 / 261
页数:12
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