REGULATED PROTEIN DELIVERY TO THE PLASMA MEMBRANE

调节蛋白质向质膜的输送

• 批准号: 6743688
• 负责人: Chris Alan Kaiser
• 金额: $ 33.85万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-02-01 至 2007-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6743688
• 关键词: Golgi apparatus; Saccharomyces cerevisiae; biological signal transduction; cell membrane; fungal genetics; gene mutation; genetic regulation; intracellular transport; laboratory rabbit; membrane proteins; nitrogen; permease; protein localization; protein transport; transcription factor; ubiquitin; vesicle /vacuole

DESCRIPTION (provided by applicant): The activities of integral membrane proteins, such as transport proteins, are often regulated by intracellular sorting. Such sorting process can produce rapid changes in the rate that a transporter is delivered to the plasma membrane in response to an intracellular signal and thus provide a way for a cell to alter its capacity to take up small molecules from the extracellular environment in response to regulatory cues. For example, the GLUT4 glucose transporter is delivered to the plasma membrane of fat and muscle cells in response to insulin, and defects in this regulated trafficking are thought to be a root cause of non insulin-dependent diabetes. Many aspects of the intracellular sorting of GLUT4 remain poorly understood at this time. Dr. Kaiser's research group proposes to continue to study regulated sorting of general amino acid permease (Gap1) in response to the nitrogen source in the growth medium. By studying amino acid permease sorting in S. cerevisiae it will be possible to apply the full power of a well developed genetic organism to elucidate the mechanisms responsible for regulated sorting in the late secretory pathway. Work in the previous funding period has identified a large set of genes that control the sorting of Gap1. These genes include factors directly involved in the membrane trafficking of Gap1, such as proteins required to modify Gap1 with poly-ubiquitin, a tag found to be required for the proper sorting between Golgi and endosomal compartments. In addition, genes required to generate the proper regulatory signals for Gap1 sorting were also identified. Building on these findings the proposal is to: (i) determine how Gap1 is ubiquitinated and to identify the cellular components required for recognition of the ubiquitin tag, (ii) use a combination of genetic and biochemical methods to characterize the gene products that control Gap1 sorting and to determine their site(s) of action in the secretory and endocytic paths, and (iii) determine how nitrogen-derived signals are generated and determine how the membrane trafficking machinery responsible for sorting Gap1 decodes these signals.

描述（由申请人提供）：整合膜蛋白（如转运蛋白）的活性通常受细胞内分选的调节。这种分选过程可以响应于细胞内信号而产生转运蛋白递送至质膜的速率的快速变化，从而为细胞提供了一种改变其响应于调节信号而从细胞外环境摄取小分子的能力的方式。例如，GLUT 4葡萄糖转运蛋白响应于胰岛素被递送到脂肪和肌肉细胞的质膜，并且这种受调节的运输中的缺陷被认为是非胰岛素依赖型糖尿病的根本原因。GLUT 4的细胞内分选的许多方面目前仍知之甚少。Kaiser博士的研究小组建议继续研究一般氨基酸通透酶（Gap1）对生长培养基中氮源的调节分选。通过对S.因此，将有可能应用发育良好的遗传生物体的全部能力来阐明负责晚期分泌途径中的调节分选的机制。上一个资助期的工作已经确定了一大组控制Gap1排序的基因。这些基因包括直接参与Gap1膜运输的因子，例如用聚泛素修饰Gap1所需的蛋白质，聚泛素是高尔基体和内体区室之间正确分选所需的标签。此外，还鉴定了产生Gap1分选的适当调控信号所需的基因。根据这些调查结果，建议：（i）确定Gap1如何被泛素化并鉴定识别泛素标签所需的细胞组分，（ii）使用遗传和生物化学方法的组合来表征控制Gap1分选的基因产物并确定它们在分泌和内吞途径中的作用位点，和（iii）确定氮源信号是如何产生的，并确定负责分选Gap1的膜运输机制如何解码这些信号。