STRUCTURE OF KINETOCHORE-MICROTUBULE INTERACTIONS

动粒-微管相互作用的结构

• 批准号: 7722826
• 负责人: MARY MORPHEW
• 金额: $ 0.92万
• 依托单位: UNIVERSITY OF COLORADO
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-01 至 2009-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7722826
• 关键词: 3-Dimensional; Binding; Cell physiology; Cells; Characteristics; Chromosomes; Computer Retrieval of Information on Scientific Projects Database; Flare; Freezing; Funding; Grant; Heterochromatin; In Vitro; Institution; Kinetochores; Methods; Microtubules; Mitotic; Mitotic spindle; Morphology; Research; Research Personnel; Resources; Source; Staging; Structure; United States National Institutes of Health; in vivo; novel; reconstruction; tomography; tool

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. We are using cryofixed, freeze-substituted cells to study the morphology of kinetochores and their associated microtubule (MT) in mitotic cells. We have developed successful methods for preparing well-frozen mitotic cells (Morphew and McIntosh, J. Micros 212:21-25). 3-D reconstructions of kinetochores from several species have been obtained using dual-axis tomography. The structures of kinetochore-associated MT ends have been oriented and extracted using the "slicer" tool in IMOD. The walls of most kinetochore MTs flare outward at their plus ends, a morphology characteristic of disassembling MTs in vitro (Mandelkow et al., JCB 114:977, 1991). The degree of flaring has been quantified and found to be similarly distributed at all mitotic stages. These findings suggest that flaring in vivo is not simply indicative of disassembly, but may reflect a different dynamic state that can be controlled by other cellular processes. The regions around kinetochore MTs contain slender fibrils that appear to connect the MT walls in the centromeric heterochromatin. These findings suggest a novel mechanism for the binding of chromosomes to the mitotic spindle.

这个子项目是许多利用 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 我们正在使用冷冻固定，冷冻替代细胞，研究有丝分裂细胞中的动粒及其相关微管（MT）的形态。我们已经开发了用于制备良好冷冻的有丝分裂细胞的成功方法（Morphew和McIntosh，J.Micros212：21-25）。使用双轴断层扫描技术已经获得了几个物种动粒的3D重建。 已被定向和提取使用IMOD中的“切片器”工具的结构的kinetochorse相关的MT结束。 大多数动粒MT的壁在其正端向外张开，这是体外分解MT的形态学特征（Mandelkow等人，JCB 114：977，1991）。扩口的程度已被量化，并发现类似地分布在所有有丝分裂阶段。 这些研究结果表明，在体内的耀斑是不是简单的解体的指示，但可能反映了不同的动态状态，可以由其他细胞过程控制。 动粒MT周围的区域含有细长的纤维，似乎连接在着丝粒异染色质中的MT壁。 这些发现提示了染色体与有丝分裂纺锤体结合的一种新机制。