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J Cell Biol. 2011 Jun 27;193(7):1229-44. doi: 10.1083/jcb.201104008. Epub 2011 Jun 20.
2
Regulation of the final stage of mitosis by components of the pre-replicative complex and a polo kinase.有丝分裂末期的调控由前复制复合物的组成成分和一个 polo 激酶来完成。
Cell Cycle. 2011 May 1;10(9):1374-7. doi: 10.4161/cc.10.9.15489.
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Activation of Cdk2/Cyclin E complexes is dependent on the origin of replication licensing factor Cdc6 in mammalian cells.在哺乳动物细胞中,Cdk2/细胞周期蛋白 E 复合物的激活依赖于复制起始因子 Cdc6。
Cell Cycle. 2010 Nov 15;9(22):4533-41. doi: 10.4161/cc.9.22.13789.
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Same partners, different dance: involvement of DNA replication proteins in centrosome regulation.相同的伙伴,不同的舞蹈:DNA 复制蛋白在中心体调控中的作用。
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5
Cell division cycle 6, a mitotic substrate of polo-like kinase 1, regulates chromosomal segregation mediated by cyclin-dependent kinase 1 and separase.细胞分裂周期蛋白 6,作为 polo 样激酶 1 的有丝分裂底物,调节细胞周期蛋白依赖性激酶 1 和 separase 介导的染色体分离。
Proc Natl Acad Sci U S A. 2010 Nov 16;107(46):19742-7. doi: 10.1073/pnas.1013557107. Epub 2010 Nov 1.
6
Nuclear and spindle positioning during oocyte meiosis.卵母细胞减数分裂过程中的核和纺锤体定位。
Curr Opin Cell Biol. 2011 Feb;23(1):78-84. doi: 10.1016/j.ceb.2010.07.008. Epub 2010 Aug 11.
7
NuMA after 30 years: the matrix revisited.核仁基质蛋白 30 年之后:重新审视核基质。
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Orc1 controls centriole and centrosome copy number in human cells.Orc1控制人类细胞中的中心粒和中心体拷贝数。
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10
Linking mitosis with S-phase: Cdc6 at play.将有丝分裂与S期联系起来:发挥作用的Cdc6蛋白。
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Cdc6 在爪蟾卵母细胞减数分裂纺锤体组装中是必需的。

Cdc6 is required for meiotic spindle assembly in Xenopus oocytes.

机构信息

Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX, USA.

出版信息

Cell Cycle. 2012 Feb 1;11(3):524-31. doi: 10.4161/cc.11.3.19033.

DOI:10.4161/cc.11.3.19033
PMID:22262174
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3315094/
Abstract

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.

摘要

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。