Mechanisms of Mitotic Fidelity

项目摘要 有丝分裂的主要目的是在两个子细胞之间准确地分配遗传物质。缺陷 减数分裂或有丝分裂导致非整倍体，这是出生缺陷的一个重要原因，也是 肿瘤发生学。这一过程的关键是有丝分裂纺锤体，这是一种细胞大分子机器 负责遗传物质的比对和分离。即使主轴结构和 分子成员在有机体中高度保守，即纺锤体和蛋白质的详细组织 即使在生物体内不同的细胞类型之间，功能也会有所不同。这种变异表明细胞已经进化 多种途径以确保遗传物质的适当分布。我的实验室长期以来一直对 了解分子马达蛋白如何组织纺锤体结构，调节微管动力学 纺锤体，并有助于有丝分裂过程中准确的染色体分离。这些研究很重要 因为马达蛋白不仅在纺锤体的组织和功能中起着基本的作用，而且还因为 它们经常在癌细胞中过度表达，可能是治疗开发的有价值的靶点。在 今后五年，我们的研究将围绕三个关键问题展开。1)分子马达在空间和空间上是如何活动的 临时管制？一个重要的目标不仅是了解分子马达是如何单独发挥作用的， 还有一组马达如何与它们的结合伙伴合作来调节纺锤体的功能。我们的研究 将定义发动机的生化活动和该活动的细胞读数之间的关键网络。2) 调控的微管动力学和中心体聚集如何提高有丝分裂的保真度？海流 模型是癌细胞产生低水平的非整倍体来推动它们的生存，同时限制严重的 确保细胞死亡的非整倍体。我们将通过以下方式揭示关键分子马达如何影响有丝分裂的保真度 剖析它们在有丝分裂和DNA损伤修复中的作用。此外，我们将研究中心体是如何 在中心体扩增的细胞中，聚集限制了严重的非整倍体。3)染色体如何准确 倍性改变的细胞中染色体负荷增加会影响分离吗？一个重要的但 未被研究的问题是阐明细胞蛋白的正常补充是如何处理非整倍体的 正常细胞和癌细胞以及关键分子相对表达水平的变化如何影响 遗传物质的准确分离。我们将利用我们的能力来生成细胞 不同水平的倍性，以了解关键分子马达表达的变化如何受 增加了染色体负荷，以及这如何影响有丝分裂的保真度。我们提议的研究利用了我们的 关键分子工具箱、严格的生化分析、高质量的成像和多样化的模型系统 定义控制有丝分裂保真度的马达和调节网络的功能。这些研究的结果 将定义不同的蛋白质相互作用网络影响纺锤体形态发生的机制 并将为细胞如何维持基因组完整性提供新的见解。

Project Summary The major goal of mitosis is to distribute the genetic material accurately between two daughter cells. Defects in meiosis or mitosis lead to aneuploidy, which is a significant cause of birth defects and is a hallmark of tumorigenesis. Critical to this process is the mitotic spindle, which is a cellular macromolecular machine tasked with both alignment and segregation of the genetic material. Even though the spindle structure and molecular players are highly conserved across organisms, the detailed organization of the spindle and protein function can vary even between cell types within an organism. This variation suggests that cells have evolved multiple pathways to ensure the proper distribution of genetic material. My lab has a long-standing interest in understanding how molecular motor proteins organize spindle structure, regulate microtubule dynamics in the spindle, and contribute to accurate chromosome segregation during mitosis. These studies are important because motor proteins not only play fundamental roles in spindle organization and function, but also because they are often overexpressed in cancer cells and may be valuable targets for therapeutic development. In the next five years, our studies will focus on three key questions. 1) How is molecular motor activity spatially and temporally regulated? An important goal is to understand not only how molecular motors function individually, but also how groups of motors cooperate with their binding partner to regulate spindle function. Our studies will define critical networks between biochemical activities of motors and cellular readouts of that activity. 2) How do regulated microtubule dynamics and centrosome clustering enhance mitotic fidelity? The current model is that cancer cells generate low levels of aneuploidy to drive their survival while limiting severe aneuploidy that would ensure cell death. We will uncover how key molecular motors impact mitotic fidelity by dissecting their function in mitosis and DNA damage repair. In addition, we will examine how centrosome clustering restricts severe aneuploidy in cells with amplified centrosomes. 3) How is accurate chromosome segregation impacted by increased chromosome load in cells with altered ploidy? An important but understudied problem is to elucidate how the normal complement of cellular proteins handles aneuploidy in both normal and cancer cells and how changes in the relative expression levels of key players impact accurate segregation of the genetic material. We will take advantage of our ability to generate cells with different levels of ploidy to understand how changing expression of key molecular motors is impacted by increased chromosome load and how that affects mitotic fidelity. Our proposed studies take advantage of our toolbox of key molecules, rigorous biochemical assays, high quality imaging, and diverse model systems to define the function of motors and regulatory networks that control mitotic fidelity. The outcome of these studies will define mechanisms by which distinct protein-protein interaction networks impact spindle morphogenesis and will provide new insights into how cells maintain genome integrity.