The Role of Cell Size and G1-phase Cdks in Cell Growth Control

细胞大小和 G1 期 Cdks 在细胞生长控制中的作用

• 批准号: 7233189
• 负责人: BRANDT L SCHNEIDER
• 金额: $ 24.42万
• 依托单位: TEXAS TECH UNIVERSITY HEALTH SCIS CENTER
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-01 至 2011-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7233189
• 关键词: Address; Affect; Biochemical Pathway; Biological Assay; Biological Models; Cancer Etiology; Causations; Cell Cycle Regulation; Cell Proliferation; Cell Size; Cell Survival; Cells; Clinical; Complex; Cues; Cyclin-Dependent Kinases; Cyclins; Data; Development; Fertilization; G1 Phase; Genetic; Genetic Screening; Genetic Transcription; Genomics; Goals; Grant; Growth; Growth Factor; Homeostasis; Interphase Cell; Intervention; Laboratories; Link; Longevity; Malignant Neoplasms; Mammalian Cell; Measures; Mitogens; Molecular Genetics; Natural regeneration; Oocytes; Pathway interactions; Phase; Phosphoric Monoester Hydrolases; Phosphotransferases; Physiological; Proliferating; Proteins; Rate; Research Personnel; Role; S-Phase Fraction; Stem cells; Stimulus; Testing; Time; Translating; Yeasts; base; cell growth; clinically relevant; design; digital; follow-up; neoplastic cell; research study; response

DESCRIPTION (provided by applicant): G1-phase cyclin dependent kinases (Cdks) are required for proliferation and normal development. The activity of these complexes is modulated predominately by growth factors and mitogens which promote proliferation by inducing the expression of G1-phase cyclins. However, the mechanisms that control the timing, expression levels, and activity of G1-phase cyclins are still not well understood. Thus, the broad and long-term goals of my laboratory are to identify and dissect the genetic, molecular and biochemical pathways that control G1-phase cyclin expression and to determine the role of G1-phase Cdks in cell growth control. Using yeast as a genetic model system, we have demonstrated that G1-phase cyclin expression, and importantly, the proliferation rate of cells, is strongly linked to cell size; large cells express G1-phase cyclins sooner and to higher levels as compared to small cells. Subsequently, large cells proliferate much more rapidly than small cells. Because G1-phase Cdks and the basic mechanisms of cell cycle control are so highly conserved, we hypothesize that mammalian cell proliferation and G1-phase cyclin expression are also linked to cell size. Moreover, since hyper-activation of G1-phase Cdks is implicated in the causation of cancer, the demonstration of a mechanistic link between cell size, G1-phase cyclin expression, and proliferation in mammalian cells will be both biologically and clinically relevant. Therefore, in this proposal, we address three questions: 1. Is proliferation rate of mammalian cells linked to cell size?, 2. How is the expression of G1-phase cyclins linked to cell size?, and 3. Does G1-phase Cdk activity link proliferation rate to cell size? Completion of the experiments proposed in this grant will greatly clarify the relationships between cell size, G1-phase Cdk activity, and the proliferative capacity of cells. We propose that linking cell size to proliferation rate using G1-phase Cdks represents an important physiological means that enables large resting cells (e.g. stem cells) to proliferate rapidly in response to stimuli-an important conserved function specific to stem cells. However, the inability to appropriately down regulate G1 -phase Cdk activity might be a cause of cancer. This exemplifies the critical importance of understanding the role of G1-phase Cdks in proliferation because this type of information is essential before effective anti-cancer clinical interventions can be designed.

描述（由申请方提供）：G1期细胞周期蛋白依赖性激酶（Cdks）是增殖和正常发育所必需的。这些复合物的活性主要由生长因子和有丝分裂原调节，所述生长因子和有丝分裂原通过诱导G1期细胞周期蛋白的表达促进增殖。然而，控制G1期细胞周期蛋白的时间，表达水平和活性的机制仍然没有得到很好的理解。因此，我实验室的广泛和长期目标是识别和剖析控制G1期细胞周期蛋白表达的遗传、分子和生化途径，并确定G1期Cdks在细胞生长控制中的作用。使用酵母作为遗传模型系统，我们已经证明，G1期细胞周期蛋白的表达，重要的是，细胞的增殖率，是密切相关的细胞大小;大细胞表达G1期细胞周期蛋白更快，更高的水平相比，小细胞。随后，大细胞比小细胞增殖快得多。由于G1期Cdks和细胞周期控制的基本机制是高度保守的，我们假设哺乳动物细胞增殖和G1期细胞周期蛋白的表达也与细胞大小有关。此外，由于G1期Cdks的过度活化与癌症的起因有关，因此在哺乳动物细胞中细胞大小、G1期细胞周期蛋白表达和增殖之间的机械联系的证明将是生物学和临床相关的。因此，在本建议中，我们解决三个问题：1。哺乳动物细胞的增殖率与细胞大小有关吗？2. G1期细胞周期蛋白的表达如何与细胞大小相关？和3. G1期Cdk活性是否将增殖速率与细胞大小联系起来？完成本研究计画的实验，将可进一步厘清细胞大小、G1期Cdk活性与细胞增殖能力之间的关系。我们建议，使用G1期Cdks连接细胞大小的增殖率代表了一个重要的生理手段，使大的静息细胞（如干细胞）迅速增殖响应刺激-一个重要的保守的功能特定于干细胞。然而，不能适当下调G1期Cdk活性可能是癌症的原因。这证明了理解G1期Cdks在增殖中的作用的至关重要性，因为在设计有效的抗癌临床干预措施之前，这种类型的信息是必不可少的。