Department of Systems Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Mol Cell Proteomics. 2010 Feb;9(2):336-50. doi: 10.1074/mcp.M900308-MCP200. Epub 2009 Sep 28.
The cytoskeleton globally reorganizes between mitosis (M phase) and cytokinesis (C phase), which presumably requires extensive regulatory changes. To reveal these changes, we undertook a comparative proteomics analysis of cells tightly drug-synchronized in each phase. We identified 25 proteins that bind selectively to microtubules in C phase and identified several novel binding partners including nucleolar and spindle-associated protein. C phase-selective microtubule binding of many of these proteins depended on activity of Aurora kinases as assayed by treatment with the drug VX680. Aurora-B binding partners switched dramatically between M phase to C phase, and we identified several novel C phase-selective Aurora-B binding partners including PRC1, KIF4, and anaphase-promoting complex/cyclosome. Our approach can be extended to other cellular compartments and cell states, and our data provide the first broad biochemical framework for understanding C phase. Concretely, we report a central role for Aurora-B in regulating the C phase cytoskeleton.
细胞骨架在有丝分裂(M 期)和胞质分裂(C 期)之间进行全局重排,这可能需要广泛的调节变化。为了揭示这些变化,我们对每个阶段都被药物紧密同步的细胞进行了比较蛋白质组学分析。我们鉴定了 25 种在 C 期选择性结合微管的蛋白质,并鉴定了几个新的结合伴侣,包括核仁与纺锤体相关蛋白。这些蛋白质中的许多 C 期选择性微管结合依赖于 Aurora 激酶的活性,这可以通过用药物 VX680 处理来测定。Aurora-B 的结合伴侣在 M 期到 C 期之间发生了剧烈的转换,我们鉴定了几个新的 C 期选择性 Aurora-B 结合伴侣,包括 PRC1、KIF4 和后期促进复合物/周期素体。我们的方法可以扩展到其他细胞区室和细胞状态,我们的数据提供了第一个广泛的生化框架来理解 C 期。具体来说,我们报告了 Aurora-B 在调节 C 期细胞骨架中的核心作用。