Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Cell Cycle. 2012 Feb 1;11(3):524-31. doi: 10.4161/cc.11.3.19033.
During the maturation of Xenopus oocytes, Cdc6 expression is necessary to establish replication competence to support early embryonic DNA replication. However, Cdc6 is expressed before the completion of MI, at a time when its function as a replication factor is not required, suggesting additional roles for Cdc6 in meiosis. Confocal immunofluorescence microscopy revealed that Cdc6 protein was distributed around the spindle precursor at the time of germinal vesicle breakdown (GVBD), and localized to the margin of the nascent spindle early in prometaphase. Cdc6 subsequently localized to spindle poles in late prometaphase, where it remained until metaphase arrest. Microinjection of antisense oligonucleotides specific for Cdc6 mRNA disrupted spindle assembly, resulting in defects including delayed spindle assembly, misoriented and unattached anaphase spindles, monasters, multiple spindles, microtubule aggregates associated with condensed chromosomes, or the absence of recognizable spindle-like structures, depending on the level of residual Cdc6 expression. Furthermore, Cdc6 co-localized with γ-tubulin in centrosomes during interphase in all somatic cells analyzed, and associated with spindle poles in mitotic COS cells. Our data suggest a role for Cdc6 in spindle formation in addition to its role as a DNA replication factor.
在非洲爪蟾卵母细胞的成熟过程中,Cdc6 的表达对于建立复制能力以支持早期胚胎 DNA 复制是必需的。然而,Cdc6 在 MI 完成之前表达,此时它作为复制因子的功能不需要,这表明 Cdc6 在减数分裂中有额外的作用。共聚焦免疫荧光显微镜显示,Cdc6 蛋白在生殖泡破裂(GVBD)时分布在纺锤体前体周围,并在早期前中期定位于新形成的纺锤体的边缘。Cdc6 随后在晚期前中期定位于纺锤体极,直到中期阻滞时仍留在那里。针对 Cdc6 mRNA 的反义寡核苷酸的显微注射破坏了纺锤体的组装,导致包括纺锤体组装延迟、取向错误和未连接的后期纺锤体、单体、多个纺锤体、与浓缩染色体相关的微管聚集物或缺乏可识别的纺锤体样结构等缺陷,这取决于残留的 Cdc6 表达水平。此外,在所有分析的体细胞中,Cdc6 在间期与中心体中的 γ-微管蛋白共定位,并在有丝分裂的 COS 细胞中与纺锤体极相关。我们的数据表明,Cdc6 除了作为 DNA 复制因子外,还在纺锤体形成中发挥作用。