Acta Biochim Biophys Sin (Shanghai). 2023 Feb 25;55(2):250-261. doi: 10.3724/abbs.2023025.
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.
E3 泛素连接酶在所有真核生物中与细胞分裂、分化和存活密切相关,并在多种生物过程和疾病中发挥关键的调节作用。Deltex2 作为 DELTEX 家族泛素连接酶的一员,其特征是具有一个 RING 结构域和一个 C 端结构域(DTC),但其在成肌分化中的功能和潜在机制尚未完全阐明。在这里,我们报告 Deltex2 在肌肉中高度表达,通过介导 Pax7 的表达来正向调节成肌细胞增殖。同时,我们发现 Deltex2 在成肌分化过程中从细胞核转位到细胞质,进一步揭示 Deltex2 抑制成肌细胞分化,并与 MyoD 相互作用,导致 MyoD 的泛素化和降解。总的来说,我们的研究结果揭示了 Deltex2 在协调成肌发生中的生理功能,并描绘了 Deltex2 作为 MyoD 蛋白稳定性的负调控因子的新作用。