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在CPAP中鉴定出一种与微管蛋白异二聚体结合并抑制微管组装的新型微管去稳定基序。

Identification of a novel microtubule-destabilizing motif in CPAP that binds to tubulin heterodimers and inhibits microtubule assembly.

作者信息

Hung Liang-Yi, Chen Hua-Ling, Chang Ching-Wen, Li Bor-Ran, Tang Tang K

机构信息

Institute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.

出版信息

Mol Biol Cell. 2004 Jun;15(6):2697-706. doi: 10.1091/mbc.e04-02-0121. Epub 2004 Mar 26.

Abstract

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.

摘要

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。

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