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PinX1是一种对精确染色体分离至关重要的新型微管结合蛋白。

PinX1 is a novel microtubule-binding protein essential for accurate chromosome segregation.

作者信息

Yuan Kai, Li Na, Jiang Kai, Zhu Tongge, Huo Yuda, Wang Chong, Lu Jing, Shaw Andrew, Thomas Kelwyn, Zhang Jiancun, Mann David, Liao Jian, Jin Changjiang, Yao Xuebiao

机构信息

Anhui Key Laboratory for Cellular Dynamics and Chemical Biology and Hefei National Laboratory for Physical Sciences at the Nanoscale, Hefei 230027, China.

出版信息

J Biol Chem. 2009 Aug 21;284(34):23072-82. doi: 10.1074/jbc.M109.001990. Epub 2009 Jun 24.

Abstract

Mitosis is an orchestration of dynamic interactions between spindle microtubules and chromosomes, which is mediated by protein structures that include the kinetochores, and other protein complexes present on chromosomes. PinX1 is a potent telomerase inhibitor in interphase; however, its function in mitosis is not well documented. Here we show that PinX1 is essential for faithful chromosome segregation. Deconvolution microscopic analyses show that PinX1 localizes to nucleoli and telomeres in interphase and relocates to the periphery of chromosomes and the outer plate of the kinetochores in mitosis. Our deletion analyses mapped the kinetochore localization domain of PinX1 to the central region and its chromosome periphery localization domain to the C terminus. Interestingly, the kinetochore localization of PinX1 is dependent on Hec1 and CENP-E. Our biochemical characterization revealed that PinX1 is a novel microtubule-binding protein. Our real time imaging analyses show that suppression of PinX1 by small interference RNA abrogates faithful chromosome segregation and results in anaphase chromatid bridges in mitosis and micronuclei in interphase, suggesting an essential role of PinX1 in chromosome stability. Taken together, the results indicate that PinX1 plays an important role in faithful chromosome segregation in mitosis.

摘要

有丝分裂是纺锤体微管与染色体之间动态相互作用的协调过程,这一过程由包括动粒在内的蛋白质结构以及染色体上存在的其他蛋白质复合物介导。PinX1在间期是一种有效的端粒酶抑制剂;然而,其在有丝分裂中的功能尚未得到充分记录。在这里,我们表明PinX1对于准确的染色体分离至关重要。去卷积显微镜分析表明,PinX1在间期定位于核仁和端粒,在有丝分裂时重新定位于染色体周边和动粒的外板。我们的缺失分析将PinX1的动粒定位结构域定位到中央区域,将其染色体周边定位结构域定位到C末端。有趣的是,PinX1的动粒定位依赖于Hec1和CENP - E。我们的生化特性分析表明,PinX1是一种新型的微管结合蛋白。我们的实时成像分析表明,通过小干扰RNA抑制PinX1会消除准确的染色体分离,并导致有丝分裂后期的染色单体桥和间期的微核,这表明PinX1在染色体稳定性中起着至关重要的作用。综上所述,结果表明PinX1在有丝分裂中准确的染色体分离中起重要作用。

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