Rattner J B, Rao A, Fritzler M J, Valencia D W, Yen T J
Department of Anatomy, University of Calgary, Alberta, Canada.
Cell Motil Cytoskeleton. 1993;26(3):214-26. doi: 10.1002/cm.970260305.
We have identified a novel .ca 400 kDa cell-cycle dependent kinetochore associated protein in human cells, designated CENP-F, using human autoimmune serum. Immunofluorescence staining using the native serum, affinity purified antibodies, or antibodies raised against a cloned portion of CENP-F first reveals CENP-F homogeneously distributed throughout the nucleus of HeLa cells in the G2 stage of the cell cycle. Progression into prophase is accompanied by the localization of CENP-F to all the kinetochore regions of the karyotype. Kinetochore association is maintained throughout metaphase, but at the onset of anaphase CENP-F is no longer detected in association with the kinetochore but is found at the spindle mid-zone. By telophase, it is concentrated into a narrow band on either side of the midbody. Studies of the interaction of CENP-F with the kinetochore indicate that this protein associates with the kinetochore independent of tubulin and dissociation is dependent on events connected with the onset of anaphase. Nuclease digestion studies and immunoelectron-microscopy indicate that CENP-F is localized to the kinetochore plates and specifically to the outer surface of the outer kinetochore plate. The distribution of CENP-F closely parallels that of another high molecular weight kinetochore associated protein, CENP-E. Comparative studies indicate that there are antibodies in the CENP-F reactive autoimmune serum that recognize determinants present in the central helical rod domain of CENP-E. Immune depletion experiments confirm that CENP-F exhibits the distribution pattern in cells that was seen with the native autoimmune serum.
我们利用人类自身免疫血清,在人类细胞中鉴定出一种新的约400 kDa的细胞周期依赖性动粒相关蛋白,命名为CENP-F。使用天然血清、亲和纯化抗体或针对CENP-F克隆片段产生的抗体进行免疫荧光染色,首先显示在细胞周期的G2期,CENP-F均匀分布于HeLa细胞的整个细胞核。进入前期时,CENP-F定位于核型的所有动粒区域。在整个中期,动粒关联得以维持,但在后期开始时,不再检测到CENP-F与动粒相关联,而是在纺锤体中区发现它。到末期,它集中在中体两侧的一条窄带上。对CENP-F与动粒相互作用的研究表明,该蛋白与动粒的关联不依赖于微管蛋白,且解离依赖于与后期开始相关的事件。核酸酶消化研究和免疫电子显微镜表明,CENP-F定位于动粒板,特别是外动粒板的外表面。CENP-F的分布与另一种高分子量动粒相关蛋白CENP-E的分布密切平行。比较研究表明,CENP-F反应性自身免疫血清中的抗体识别CENP-E中央螺旋杆结构域中存在的决定簇。免疫耗竭实验证实,CENP-F在细胞中呈现出与天然自身免疫血清所见相同的分布模式。