Hung Liang-Yi, Chen Hua-Ling, Chang Ching-Wen, Li Bor-Ran, Tang Tang K
Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Mol Biol Cell. 2004 Jun;15(6):2697-706. doi: 10.1091/mbc.e04-02-0121. Epub 2004 Mar 26.
We have previously identified a new centrosomal protein, centrosomal protein 4.1-associated protein (CPAP), which is associated with the gamma-tubulin complex. Here, we report that CPAP carries a novel microtubule-destabilizing motif that not only inhibits microtubule nucleation from the centrosome but also depolymerizes taxol-stabilized microtubules. Deletion mapping and functional analyses have defined a 112-residue CPAP that is necessary and sufficient for microtubule destabilization. This 112-residue CPAP directly recognizes the plus end of a microtubule and inhibits microtubule nucleation from the centrosome. Biochemical and functional analyses revealed that this 112-residue CPAP also binds to tubulin dimers, resulting in the destabilization of microtubules. Using the tetracycline-controlled system (tet-off), we observed that overexpression of this 112-residue CPAP inhibits cell proliferation and induces apoptosis after G2/M arrest. The possible mechanisms of how this 112-residue motif in CPAP that inhibits microtubule nucleation from the centrosome and disassembles preformed microtubules are discussed.
我们之前鉴定出一种新的中心体蛋白,即中心体蛋白4.1相关蛋白(CPAP),它与γ-微管蛋白复合体相关。在此,我们报告CPAP带有一个新的微管去稳定化基序,该基序不仅抑制中心体的微管成核,还能使紫杉醇稳定的微管解聚。缺失图谱分析和功能分析确定了一个112个残基的CPAP,它对于微管去稳定化是必需且充分的。这个112个残基的CPAP直接识别微管的正端并抑制中心体的微管成核。生化和功能分析表明,这个112个残基的CPAP也与微管蛋白二聚体结合,导致微管去稳定化。使用四环素调控系统(tet-off),我们观察到这个112个残基的CPAP过表达会抑制细胞增殖并在G2/M期阻滞后诱导细胞凋亡。我们讨论了CPAP中这个112个残基基序抑制中心体微管成核并拆解已形成微管的可能机制。