Regulation of Chromosome Segregation in Human Cells

人体细胞染色体分离的调控

• 批准号: 8286240
• 负责人: Prasad V Jallepalli
• 金额: $ 38.74万
• 依托单位: SLOAN-KETTERING INST CAN RESEARCH
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-07-01 至 2014-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8286240
• 关键词: Address; Alleles; Amino Acids; Anaphase; Aneuploidy; Binding; Biochemical; Biological Assay; Biological Process; Caspase; Cell division; Cells; Centrosome; Chromosome Segregation; Chromosomes; Complex; Cysteine Protease; Cytoplasm; Data; Defect; Disease; Dissection; Down Syndrome; Drosophila genus; Employee Strikes; Eukaryota; Gene-Modified; Genetic; Goals; Grant; Health; Human; Human Chromosomes; In Vitro; Kinetochores; Label; Laboratories; Length; Light; Link; MG132; Malignant Neoplasms; Maps; Mass Spectrum Analysis; Mediating; Mediator of activation protein; Methods; Microscopy; Microtubules; Mitosis; Mitotic spindle; Modeling; Molecular; Mutate; Normal Cell; Pharmacopoeias; Phenotype; Phosphorylation; Phosphorylation Site; Phosphotransferases; Poison; Prometaphase; Proteasome Inhibitor; Protein Kinase; Reaction Time; Recombinants; Regulation; Resistance; Resolution; Risk; Role; Signal Transduction; Somatic Cell; Testing; Trypsin; Tubulin; Work; anaphase-promoting complex; base; cancer cell; chemical genetics; functional genomics; homologous recombination; human PLK1 protein; human disease; improved; in vivo; inhibitor/antagonist; insight; mutant; neoplastic; novel; polo-like kinase kinase 1; public health relevance; purine analog; research study; segregation; separase; tumor

DESCRIPTION (provided by applicant): The long-term goal of this grant is to elucidate the molecules and mechanisms that sustain the accuracy of chromosome segregation. Such information is crucial for maintaining and improving human health, as inaccurate segregation causes aneuploidy and contributes to disorders like Down Syndrome and cancer. To facilitate the dissection of this and other complex biological processes, our laboratory has developed novel methods for precisely deleting or modifying genes in human somatic cells via homologous recombination. By combining these methods with high-resolution microscopy and chemical genetics, we have identified novel functions and regulation of the protein kinases Plk1 (Polo-like kinase 1) and Mps1, which are essential regulators of mitosis and cell division in all eukaryotes. Based on our preliminary findings, three aims are proposed for the next grant period: (1) to elucidate the effectors and mechanism of Plk1-dependent centrosome maturation; (2) to test Mps1's contribution to the cytosolic and kinetochore-dependent branches of the spindle assembly checkpoint (SAC); and (3) to identify the substrates of Mps1 that mediate the kinase's functions in SAC enforcement and chromosome bi-orientation. These studies will illuminate the mechanisms that regulate and sustain the high fidelity of chromosome segregation in humans. Such information is crucial for understanding how normal cells avoid aneuploidy and its adverse impacts on human health, and for developing novel treatments that specifically target aneuploidy in the context of disease. PUBLIC HEALTH RELEVANCE: Errors in chromosome segregation result in aneuploidy, an abnormal genetic configuration strongly associated with human disease, including Down Syndrome and cancer. There is a strong need to elucidate how chromosome segregation is controlled at the molecular level, both to reduce the likelihood of aneuploidy in normal cells, and to exploit aneuploidy as an "Achilles heel" in cancer cells. During the next grant period we focus specifically on the roles of two master kinases - Plk1 and Mps1 - in human chromosome segregation. As these kinases are overproduced in tumors and being evaluated as targets for anti-neoplastic therapy, our studies have strong relevance to ongoing efforts to expand and improve the cancer pharmacopeia.

描述（由申请人提供）：该基金的长期目标是阐明维持染色体分离准确性的分子和机制。这些信息对于维持和改善人类健康至关重要，因为不准确的分离会导致非整倍体，并导致唐氏综合症和癌症等疾病。为了便于解剖这个和其他复杂的生物过程，我们的实验室已经开发了新的方法，通过同源重组精确删除或修改人体细胞中的基因。通过将这些方法与高分辨率显微镜和化学遗传学相结合，我们已经确定了蛋白激酶Plk 1（Polo样激酶1）和Mps 1的新功能和调节，这是所有真核生物中有丝分裂和细胞分裂的重要调节因子。基于我们的初步研究结果，我们提出了下一个资助期的三个目标：（1）阐明Plk 1依赖的中心体成熟的效应子和机制;（2）检测Mps 1对纺锤体组装检查点（SAC）的胞质和着丝粒依赖分支的贡献;（3）确定Mps 1的底物，这些底物介导激酶在SAC实施和染色体双向定位中的功能。这些研究将阐明调节和维持人类染色体分离高保真度的机制。这些信息对于理解正常细胞如何避免非整倍性及其对人类健康的不利影响，以及开发在疾病背景下特异性靶向非整倍性的新治疗方法至关重要。 公共卫生相关性：染色体分离的错误导致非整倍体，这是一种与人类疾病（包括唐氏综合症和癌症）密切相关的异常遗传构型。有一个强烈的需要，以阐明如何在分子水平上控制染色体分离，以减少在正常细胞中的非整倍性的可能性，并利用非整倍性作为癌细胞中的“阿喀琉斯之踵”。在下一个资助期间，我们特别关注两个主激酶-Plk 1和Mps 1-在人类染色体分离中的作用。由于这些激酶在肿瘤中过量产生，并被评估为抗肿瘤治疗的靶点，我们的研究与正在进行的扩大和改善癌症药典的努力具有很强的相关性。