Dissection of the mitotic checkpoint component BUBR1

有丝分裂检查点组件 BUBR1 的解剖

• 批准号: 6551668
• 负责人: Yinghui Mao
• 金额: $ 3.83万
• 依托单位: LUDWIG INSTITUTE FOR CANCER RES LTD
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-09-01 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/6551668
• 关键词: Xenopus oocyte; biological signal transduction; cell cycle; centromere; chromosomes; enzyme activity; intermolecular interaction; kinesin; microtubules; mitotic spindle apparatus; phosphotransferases; postdoctoral investigator; protein protein interaction; protein structure function

DESCRIPTION (provided by applicant): Eukaryotic organisms have evolved a "mitotic checkpoint" to monitor the metaphase-anaphase transition in order to assure high fidelity transmission of genetic information to daughter cells. This checkpoint prevents progression through mitosis prior to attachment of every centromere to microtubules of the mitotic spindle. In attempting to identify how checkpoint signaling is linked to microtubule attachment, earlier work from the Cleveland lab has proposed that the centromere- bound microtubule motor CENP-E is one link which provides microtubule attachment, relaying this to the centromere-bound checkpoint kinase BUBR1. The focus of this proposal is to test this model for CENP-E involvement in linking the vertebrate checkpoint to microtubule attachment, focusing on the ability to manipulate the cell cycle in vitro (using Xenopus egg extracts).

描述(由申请人提供)： 真核生物已经进化出一个“有丝分裂检查点”来监控中期到后期的转变，以确保遗传信息高保真地传递到子细胞。这个检查点防止在每个着丝粒附着到有丝分裂纺锤体的微管之前通过有丝分裂进行进展。在试图确定检查点信号如何与微管附着有关的过程中，克利夫兰实验室的早期工作提出，着丝粒结合的微管发动机CENP-E是提供微管附着的一个环节，将其传递给着丝粒结合的检查点激酶BUBR1。这项提议的重点是测试CENP-E参与将脊椎动物检查点与微管连接联系起来的模型，重点是体外操纵细胞周期的能力(使用非洲爪哇卵提取液)。