Studying the control of Cytokinesis as an Evolved Complex System

研究细胞分裂作为进化复杂系统的控制

• 批准号: 7905029
• 负责人: WILLIAM J BOSL
• 金额: $ 31.94万
• 依托单位: STOWERS INSTITUTE FOR MEDICAL RESEARCH
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-08-01 至 2012-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7905029
• 关键词: Accounting; Actomyosin; Address; Aneuploidy; Animal Model; Animals; Behavior; Binding; Biochemical; CDC2 Protein Kinase; Caenorhabditis elegans; Cell Cycle; Cell Nucleolus; Cell division; Cells; Cellular biology; Chromosome Segregation; Code; Complex; Controlled Study; Cytokinesis; Cytoskeletal Proteins; Development; Disabled Persons; Embryo; Embryonic Development; Ensure; Event; Evolution; Expert Systems; Failure; Feedback; Fright; Gene Expression; Generations; Genes; Genetic; Genomic Instability; Genomics; Goals; Growth and Development function; Guanosine Triphosphate Phosphohydrolases; Hybrids; Image; Individual; Link; Malignant Neoplasms; Mitosis; Mitotic; Modeling; Molecular; Monitor; Motor; Mutation; Myosin Type II; Nature; Nematoda; Noise; Null Lymphocytes; Organism; Output; Pathway interactions; Phosphorylation; Polyploidy; Process; Protein phosphatase; Quantitative Microscopy; RNA; Reaction; Regulation; Saccharomycetales; Signal Transduction; Signaling Molecule; Simulate; System; Testing; Time; Variant; Work; Yeasts; base; biological systems; cancer cell; complex biological systems; controlled release; design; disorder prevention; driving force; experimental analysis; flexibility; genetic manipulation; models and simulation; network models; public health relevance; research study; response; tool; tumorigenesis

DESCRIPTION (provided by applicant): The broad goal of the work proposed in this application is to understand the design principles and evolutionary dynamics of the cytokinesis pathway using the budding yeast as the model organism. Cytokinesis the physical division of a cell in two is the last critical step of cell division. The complexity and importance of this process has made cytokinesis one of the extensively studied and yet still unsolved problems in cell biology. We and others previously showed that the budding yeast utilizes an actomyosin-based contractile ring to divide, as in animal cells. This finding allows us to use this highly tractable model to understand the basic principles and molecular pathways governing cytokinesis. Whereas our previous work followed a conventional approach of classical genetic and biochemical analyses, here we propose to take a unique combination of network modeling, quantitative imaging, evolutionary analysis, and genomic and expression microarrays, to understand the design principles underlying the molecular complexity. The main questions to be answered in this study are: 1) how a complex network of molecular interactions, involving signaling molecules and cytoskeletal proteins, which occur during mitosis, ensures asymmetric cell division in a spatially and temporally precise manner; and 2) how, in response to large perturbations, this cell division system could rapidly evolve to maintain its required functionality. PUBLIC HEALTH RELEVANCE: Cytokinesis is a crucial event in cell division, which is the basis for the growth and development of eukaryotic organisms. Failure in cytokinesis results in polyploidization, a common feature of cancer cells that is thought to contribute to genome instability and somatic evolution of cancer.1, 2. Asymmetric cytokinesis is also important for the generation of embryonic asymmetry and differentiation of diverse cell types3. Therefore, understanding the mechanism and regulation of cytokinsesis is important for treatment or prevention of diseases such as cancer and developmental abnormalities. 1.. Storchova, Z. & Pellman, D. From polyploidy to aneuploidy, genome instability and cancer. Nat Rev Mol Cell Biol 5, 45-54 (2004). 2.. Fujiwara, T. et al. Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells. Nature 437, 1043-1047 (2005). 3. Strome, S. Generation of cell diversity during early embryogenesis in the nematode Caenorhabditis elegans embryos. Int. Rev. Cyt. 114, 81-123 (1989).

描述（由申请人提供）：本申请中提出的工作的总体目标是了解以出芽酵母为模式生物的细胞分裂途径的设计原理和进化动力学。细胞质分裂——细胞一分为二的物理分裂——是细胞分裂的最后一个关键步骤。这一过程的复杂性和重要性使细胞分裂成为细胞生物学中被广泛研究但仍未解决的问题之一。我们和其他人先前表明，芽殖酵母利用基于肌动球蛋白的收缩环进行分裂，就像在动物细胞中一样。这一发现使我们能够使用这个高度易于处理的模型来理解细胞分裂的基本原理和分子途径。鉴于我们之前的工作遵循经典遗传和生化分析的传统方法，在这里，我们建议采用网络建模，定量成像，进化分析以及基因组和表达微阵列的独特组合，以了解分子复杂性背后的设计原则。本研究中需要回答的主要问题是：1)有丝分裂过程中发生的复杂分子相互作用网络，包括信号分子和细胞骨架蛋白，如何确保细胞在空间和时间上精确的不对称分裂；2)如何应对大的扰动，这种细胞分裂系统能够快速进化以维持其所需的功能。公共卫生相关性：细胞分裂是细胞分裂的关键事件，是真核生物生长发育的基础。细胞质分裂失败导致多倍体化，这是癌细胞的一个共同特征，被认为有助于基因组不稳定和癌症的体细胞进化。1、2。不对称胞质分裂对胚胎不对称的产生和不同细胞类型的分化也很重要3。因此，了解细胞分裂的机制和调控对治疗或预防癌症和发育异常等疾病具有重要意义。1 . .从多倍体到非整倍体，基因组不稳定性与癌症。中华生物医学工程学报，5(2),2004。2.． 藤原，T.等。细胞分裂失败产生四倍体促进p53-null细胞的肿瘤发生。自然，437,1043-1047（2005）。3. 秀丽隐杆线虫胚胎早期胚胎发生过程中细胞多样性的产生。Int。修订版，114,81-123（1989）。