Department of Prosthodontics, Peking University School and Hospital of Stomatology, National Engineering Laboratory for Digital and Material Technology of Stomatology, National Clinical Research Center for Oral Diseases, Beijing Key Laboratory of Digital Stomatology, Beijing, China.
EMBO Rep. 2021 Sep 6;22(9):e52576. doi: 10.15252/embr.202152576. Epub 2021 Aug 12.
The E3 ubiquitin ligase complex CDC20-activated anaphase-promoting complex/Cyclosome (APC/C ) plays a critical role in governing mitotic progression by targeting key cell cycle regulators for degradation. Cell division cycle protein 20 homolog (CDC20), the co-activator of APC/C, is required for full ubiquitin ligase activity. In addition to its well-known cell cycle-related functions, we demonstrate that CDC20 plays an essential role in osteogenic commitment of bone marrow mesenchymal stromal/stem cells (BMSCs). Cdc20 conditional knockout mice exhibit decreased bone formation and impaired bone regeneration after injury. Mechanistically, we discovered a functional interaction between the WD40 domain of CDC20 and the DNA-binding domain of p65. Moreover, CDC20 promotes the ubiquitination and degradation of p65 in an APC11-dependent manner. More importantly, knockdown of p65 rescues the bone loss in Cdc20 conditional knockout mice. Our current work reveals a cell cycle-independent function of CDC20, establishes APC11 as a pivotal regulator for bone formation by governing the ubiquitination and degradation of p65, and may pave the way for treatment of bone-related diseases.
E3 泛素连接酶复合物 CDC20 激活的有丝分裂后期促进复合物/细胞周期蛋白体 (APC/C) 通过靶向关键细胞周期调节剂进行降解,在调控有丝分裂进程中起着关键作用。细胞分裂周期蛋白 20 同源物 (CDC20) 是 APC/C 的共激活因子,其对于泛素连接酶的完全活性是必需的。除了其众所周知的与细胞周期相关的功能外,我们还证明 CDC20 在骨髓间充质基质/干细胞 (BMSCs) 的成骨分化中起着至关重要的作用。Cdc20 条件性敲除小鼠表现出骨形成减少和损伤后骨再生受损。在机制上,我们发现了 CDC20 的 WD40 结构域与 p65 的 DNA 结合结构域之间的功能相互作用。此外,CDC20 以 APC11 依赖性方式促进 p65 的泛素化和降解。更重要的是,p65 的敲低可挽救 Cdc20 条件性敲除小鼠的骨丢失。我们目前的工作揭示了 CDC20 的细胞周期非依赖性功能,确立了 APC11 通过调控 p65 的泛素化和降解来作为骨形成的关键调节剂,并可能为治疗与骨相关的疾病铺平道路。