Shi Xingjuan, Yao Yanjun, Wang Yujue, Zhang Yu, Huang Qinghai, Zhou Jun, Liu Min, Li Dengwen
Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, Nanjing 210096, China.
Key Laboratory of Developmental Genes and Human Disease, Institute of Life Sciences, Southeast University, Nanjing 210096, China.
FEBS Lett. 2015 Jul 8;589(15):1771-7. doi: 10.1016/j.febslet.2015.06.017. Epub 2015 Jun 22.
Microtubules, highly dynamic components of the cytoskeleton, are involved in mitosis, cell migration and intracellular trafficking. Our previous work has shown that the centrosomal protein Cep70 regulates microtubule organization and mitotic spindle orientation in mammalian cells. However, it remains elusive whether Cep70 is implicated in microtubule stability. Here we demonstrate that Cep70 enhances microtubule resistance to cold or nocodazole treatment. Our data further show that Cep70 promotes microtubule stability by regulating tubulin acetylation, and plays an important role in stabilizing microtubules. Mechanistic studies reveal that Cep70 interacts and colocalizes with histone deacetylase 6 (HDAC6) in the cytoplasm. These findings suggest that Cep70 promotes microtubule stability by interaction with HDAC6 and regulation of tubulin acetylation.
微管是细胞骨架中高度动态的组成部分,参与有丝分裂、细胞迁移和细胞内运输。我们之前的工作表明,中心体蛋白Cep70调节哺乳动物细胞中的微管组织和有丝分裂纺锤体方向。然而,Cep70是否与微管稳定性有关仍不清楚。在这里,我们证明Cep70增强了微管对低温或诺考达唑处理的抗性。我们的数据进一步表明,Cep70通过调节微管蛋白乙酰化来促进微管稳定性,并在稳定微管中发挥重要作用。机制研究表明,Cep70在细胞质中与组蛋白脱乙酰酶6(HDAC6)相互作用并共定位。这些发现表明,Cep70通过与HDAC6相互作用和调节微管蛋白乙酰化来促进微管稳定性。