Liu Yan, Wang Yin, Du Zhanwen, Yan Xiaoli, Zheng Pan, Liu Yang
Center for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, Washington, DC 20010, USA.
Center for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, Washington, DC 20010, USA.
Cell Rep. 2016 May 3;15(5):1111-1122. doi: 10.1016/j.celrep.2016.03.083. Epub 2016 Apr 21.
Fbxo30 is an orphan member of the F-box protein family with no known substrate or function. Here we report that, while Fbxo30(-/-) mice exhibit normal development, growth, lifespan, and fertility, the females fail to nurture their offspring as a result of defective mammopoiesis. Mass spectrometry analysis of Fbxo30-associated proteins revealed that Fbxo30 specifically interacts with the bipolar spindle kinesin EG5 (encoded by Kif11). As a result, Fbxo30 targets Eg5 for ubiquitinylation and controls its oscillation during the cell cycle. Correlated with EG5 dysregulation, Fbxo30(-/-) mammary epithelial cells exhibit multiple defects in centrosome homeostasis, mitotic spindle formation, and proliferation. Effects on proliferation, centrosome homeostasis, and mammopoiesis in the Fbxo30(-/-) mice were rescued through normalization of Eg5 activity using shRNA and/or an EG5 inhibitor. Our data reveal the Fbxo30-Eg5 interaction as a critical checkpoint in mammopoiesis and a critical role for ubiquitinylation-regulated Eg5 oscillation in the cell cycle.
Fbxo30是F-box蛋白家族的一个孤立成员,其底物或功能均未知。在此我们报告,虽然Fbxo30基因敲除小鼠表现出正常的发育、生长、寿命和生育能力,但雌性小鼠由于乳腺生成缺陷而无法哺育后代。对与Fbxo30相关蛋白的质谱分析表明,Fbxo30特异性地与双极纺锤体驱动蛋白EG5(由Kif11编码)相互作用。因此,Fbxo30将Eg5靶向泛素化,并在细胞周期中控制其振荡。与EG5失调相关,Fbxo30基因敲除的乳腺上皮细胞在中心体稳态、有丝分裂纺锤体形成和增殖方面表现出多种缺陷。通过使用shRNA和/或EG5抑制剂使Eg5活性正常化,挽救了Fbxo30基因敲除小鼠在增殖、中心体稳态和乳腺生成方面的影响。我们的数据揭示了Fbxo30-Eg5相互作用是乳腺生成中的一个关键检查点,以及泛素化调节的Eg5在细胞周期中的振荡的关键作用。