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Mechanisms of Microtubule Dynamic Turnover

Mechanisms of Microtubule Dynamic Turnover
微管动态周转机制
批准号:
7924941
负责人:
Patricia Wadsworth
金额:
$21.61万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-07-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Microtubules are dynamic cytoskeletal polymers that are required for mitosis, organelle motility and the establishment and maintenance of cell form. The microtubule cytoskeleton is dramatically reorganized each cell cycle: the extensive interphase microtubule array is replaced with a bipolar mitotic spindle, which is responsible for the accurate segregation of the duplicated chromosomes into two daughter cells during mitosis. The mitotic spindle is disassembled at the end of mitosis and the interphase microtubule array reformed. The long-term goal of our work is to understand how cells accomplish the remodeling of the microtubule array during each cell cycle. A key feature of our experimental approach is the analysis of microtubule behavior in living cells. In the proposed experiments, marks on the microtubule lattice will be created by local photoactivation of cells expressing tubulin tagged with a photoactivatible GFP variant. Chromosome motion will be monitored simultaneously using a GFPMicrotubules GFP-tagged kinetochore protein, CenpA. The movement of the photoactivated marks at prophase will be characterized and their role in nuclear envelope breakdown determined. The role of the centrosome in spindle microtubule movements will be examined by comparison of microtubule behavior in cells containing and lacking centrosomes. To determine the molecular motor proteins that are responsible for microtubule movements, individual mitotic motor proteins will be inactivated using post-transcriptional gene silencing, or RNAi. Cytoskeletal organization will be examined in fixed preparations using 3-D reconstructions of Z-series of images. The results will provide new information about the molecular basis for microtubule motions during spindle assembly and how these motions contribute to chromosome motion during mitosis. Learning how normal cells construct a mitotic spindle is an important first step towards understanding defective cell division in cancer.
期刊论文(19)
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科研奖励(0)
会议论文
Using Fluorescence Microscopy to Study Mitosis.
使用荧光显微镜研究有丝分裂。
DOI: 10.1007/978-1-4939-3542-0_1
发表时间: 2016
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Balchand,SaiK, Mann,BarbaraJ, Wadsworth,Patricia]
通讯作者: Wadsworth,Patricia
Mitotic functions of kinesin-5.
驱动蛋白-5 的有丝分裂功能。
DOI: 10.1016/j.semcdb.2010.01.019
发表时间: 2010-05
期刊: Seminars in cell & developmental biology
影响因子: 7.3
作者: [Ferenz NP, Gable A, Wadsworth P]
通讯作者: Wadsworth P
DOI: 10.1016/j.cub.2008.12.026
发表时间: 2009-02-24
期刊: Current biology : CB
影响因子: --
作者: [Bezanilla M, Wadsworth P]
通讯作者: Wadsworth P
Living microlens arrays.
活体微透镜阵列。
DOI: 10.1002/cm.20302
发表时间: 2008
期刊: Cell motility and the cytoskeleton
影响因子: --
作者: [Zimberlin,JessicaA, Wadsworth,Patricia, Crosby,AlfredJ]
通讯作者: Crosby,AlfredJ
12
    Purchase of Leica TCS SP2 Confocal Microscope
    Mechanisms of Microtubule Dynamic Turnover
    MECHANISM AND REGULATION OF MICROTUBULE TURNOVER
    Mechanisms of Microtubule Dynamic Turnover
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