Assembly and Placement of the Cell Division Ring

细胞分裂环的组装和放置

• 批准号: 8000046
• 负责人: Fred Chang
• 金额: $ 10.44万
• 依托单位: COLUMBIA UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-01-14 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8000046
• 关键词: Actins; Animal Model; Cell Cycle; Cell Cycle Regulation; Cell Nucleus; Cell division; Cell physiology; Cell surface; Cells; Cellular Structures; Cellular biology; Complex; Cues; Cytokinesis; Data; Deposition; Development; Disease; Event; Filopodia; Fission Yeast; Fluorescence Microscopy; G2 Phase; Genetic; Growth; Human; Infertility; Interphase; Life; Link; Malignant Neoplasms; Medial; Microtubules; Molecular; Morphogenesis; Nuclear; Pattern; Phase; Phosphorylation; Plus End of the Microtubule; Positioning Attribute; Process; Protein Kinase; Proteins; Regulation; Site; Specific qualifier value; Stress Fibers; Structure; Testing; Time; Work; base; cancer cell; cell assembly; cell growth; cell type; deafness; follow-up; human disease; in vivo; inhibitor/antagonist; overexpression; polarized cell

DESCRIPTION (provided by applicant): Diverse actin structures drive the ability of cells to polarize, crawl, communicate and divide. The assembly of many of these actin structures depends on the actin nucleating proteins, the formins. A key question is how formins are positioned and regulated to build actin structures at specific sites on the cell surface at the right times. We study cell polarization and cytokinesis in fission yeast Schizosaccharomyces pombe, and focus on the regulation and function of formins. Microtubules regulate the formin forSp and actin cable assembly for cell polarization, through microtubule plus end proteins teal p and tea4p. The nucleus regulates the positioning of the cytokinesis formin cdc12p and the actin contractile ring through a nuclear shuttling protein mid1p. In addition to just actin assembly, our preliminary results suggest that formins have key regulatory functions in initiating cell polarization and cytokinesis. Our specific aims focus on the dissecting that the molecular links and regulatory networks underlying these fundamental processes. Cell division and polarization are universal, cellular processes that serve as the basis for cellular function and proliferation. Mistakes, for instance, in cytokinesis are likely to contribute to the development of the cancer cell. These studies using fission yeast as a model organism are highly relevant towards understanding human cell biology and disease.

描述（由申请人提供）：多样化的肌动蛋白结构驱动细胞极化、爬行、交流和分裂的能力。许多肌动蛋白结构的组装取决于肌动蛋白成核蛋白，即福尔明。一个关键问题是如何定位和调节福尔明以在正确的时间在细胞表面的特定位点构建肌动蛋白结构。我们研究裂殖酵母裂殖酵母的细胞极化和胞质分裂，并重点关注福尔明的调节和功能。微管通过微管加上末端蛋白 teal p 和 tea4p 调节 forSp 和肌动蛋白电缆组件以实现细胞极化。细胞核通过核穿梭蛋白 mid1p 调节胞质分裂 formin cdc12p 和肌动蛋白收缩环的定位。除了肌动蛋白组装之外，我们的初步结果表明福明在启动细胞极化和胞质分裂方面具有关键的调节功能。我们的具体目标集中于剖析这些基本过程背后的分子联系和调控网络。细胞分裂和极化是普遍的细胞过程，是细胞功能和增殖的基础。例如，胞质分裂中的错误可能会导致癌细胞的发展。这些使用裂殖酵母作为模式生物的研究与理解人类细胞生物学和疾病高度相关。