Centrosome Structure, Function and Duplication

中心体结构、功能和复制

• 批准号: 6928858
• 负责人: Tim Stearns
• 金额: $ 37.48万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1995
• 资助国家: 美国
• 起止时间: 1995-08-01 至 2009-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6928858
• 关键词: Xenopus oocyte; antibody; cell component structure /function; cell cycle; cell fusion; cell line; centrosome; cilium; crosslink; cyclin dependent kinase; diploidy; immunofluorescence technique; kinase inhibitor; laboratory rabbit; microtubules; neoplastic cell; tubulin

DESCRIPTION (provided by applicant): The central problems addressed in the proposed research are how the centrosome is assembled, how it duplicates once per cell cycle, and what happens in cells in which centrosome number is aberrant. The centrosome nucleates microtubules and organizes those microtubules to create a useful array. The centrosome is the major microtubule organizing center in animal cells, and is present in a single copy at the beginning of the cell cycle. The centrosome duplicates in S phase, and the two resulting centrosomes help to organize the two poles of the mitotic spindle. Work from my lab and others over the last ten years has identified molecules involved in microtubule nucleation, the central regulators of centrosome duplication, important structural proteins involved in duplication, and control mechanisms that control centrosome number and link the centrosome and the cell cycle. Interest in the centrosome has grown recently because a correlation has been established between centrosome abnormalities and the development of cancer. Cancer cells often have extra centrosomes, which is likely to contribute to the genomic instability and rapid evolution characteristic of this disease. The proposed experiments make use of the strengths that we have developed in reagents and assays for studying centrosome structure, function and duplication. I address four specific aims in this proposal: 1) Characterize the block to centrosome reduplication. We will test models for the mechanism of the block, determine whether cancer cells have defects in the block, and test whether the block can be overcome by manipulation of potential regulators. 2) Investigate the relationship between centrosome number, ploidv, and genome instability. We will use cell fusion methods to create cells of defined centrosome number and ploidy, examine the progression and outcome of mitosis in these cells, and compare normal and cancer cells in their response to centrosome and ploidy abnormalities. 3) Define the molecular interactions of the gamma-tubulin ring complex with microtubules and with the centrosome. We will use purified components to determine the molecular interactions between the gamma-tubulin ring complex, the microtubule, and the centrosome. 4) Investigate the role of delta-tubulin and epsilon-tubulin in centrosome function and duplication. We will characterize the interactions between delta-tubulin, epsilon-tubulin and the other known tubulins, and define the function of delta-tubulin in vitro using assays in frog egg extracts, and in vivo in human cells.

描述（由申请人提供）：拟议研究中解决的核心问题是中心体如何组装，每个细胞周期如何复制一次，以及中心体数量异常的细胞中会发生什么。中心体使微管成核并组织这些微管以形成有用的阵列。中心体是动物细胞中主要的微管组织中心，在细胞周期开始时以单个副本存在。中心体在S期复制，产生的两个中心体有助于组织有丝分裂纺锤体的两个极。我的实验室和其他人在过去十年的工作已经确定了参与微管成核的分子、中心体复制的中央调节因子、参与复制的重要结构蛋白，以及控制中心体数量和连接中心体与细胞周期的控制机制。最近人们对中心体的兴趣日益浓厚，因为中心体异常与癌症发展之间存在相关性。癌细胞通常具有额外的中心体，这可能导致这种疾病的基因组不稳定和快速进化特征。所提出的实验利用了我们在研究中心体结构、功能和复制的试剂和测定中开发的优势。我在此提案中阐述了四个具体目标： 1) 表征中心体重复的块。我们将测试阻断机制的模型，确定癌细胞在阻断中是否存在缺陷，并测试是否可以通过操纵潜在的调节因子来克服阻断。 2) 研究中心体数量、倍体和基因组不稳定性之间的关系。我们将使用细胞融合方法来创建具有确定中心体数量和倍性的细胞，检查这些细胞有丝分裂的进展和结果，并比较正常细胞和癌细胞对中心体和倍性异常的反应。 3) 定义γ-微管蛋白环复合物与微管和中心体的分子相互作用。我们将使用纯化的成分来确定 γ-微管蛋白环复合物、微管和中心体之间的分子相互作用。 4) 研究δ-微管蛋白和ε-微管蛋白在中心体功能和复制中的作用。我们将描述 δ-微管蛋白、ε-微管蛋白和其他已知微管蛋白之间的相互作用，并使用青蛙卵提取物的体外测定和人体细胞的体内测定来定义 δ-微管蛋白的功能。