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The endomembrane system of all eukaryotic cells consists of a collection of membrane bound compartments. Movement of materials amongst these compartments is achieved by the regulated trafficking of cargo vesicles between compartments. In the process of differentiation, higher cells re-organize their internal membranes in an enormous variety of ways; expanding or specializing certain compartments, distributing them differently in the cell, or carrying vesicles to new destinations. Though these rearrangements are often critical to the function of the differentiated cell, little is known about how these specializations are imposed on the basic pattern of the secretory pathway. Spore formation in yeast involves a cell division that requires a similar organized rearrangement of the secretory apparatus. In this instance, retargetting of secretory vesicles gives rise to a new membrane compartment, the prospore membrane. This membrane arises by the redirection of secretory vesicles away from the plasma membrane to the cell interior. Prospore membrane formation therefore serves as a model for understanding the developmental^ programmed reorganization of cellular membranes. In addition to the retargetting of secretory vesicles, new genetic requirements are imposed on the fusion and trafficking of these vesicles during sporulation. During the initial coalescence of vesicles into a membrane sheet, fusion of the vesicles requires a specialized docking complex, specific fusion proteins, and a lipid modifying enzyme. We are using a combination of genetic and cell biological approaches to understand how these different activities interact to allow the de novo formation of a new membrane compartment. Once an initial membrane sheet is formed, fusion of vesicles to the membrane is controlled by a distinct set of proteins. The basis for this change is also under investigation. Together these studies will provide insight into how the cell modifies its basic architecture during differentiation.
期刊论文(14)
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Genetic evidence of a role for membrane lipid composition in the regulation of soluble NEM-sensitive factor receptor function in Saccharomyces cerevisiae.
膜脂成分在酿酒酵母可溶性 NEM 敏感因子受体功能调节中的作用的遗传证据。
DOI: 10.1534/genetics.166.1.89
发表时间: 2004
期刊: Genetics
影响因子: 3.3
作者: [Coluccio,Alison, Malzone,Maria, Neiman,AaronM]
通讯作者: Neiman,AaronM
DOI: 10.1091/mbc.e09-10-0842
发表时间: 2010-04-01
期刊: Molecular biology of the cell
影响因子: 3.3
作者: [Yang HJ, Neiman AM]
通讯作者: Neiman AM
Binding interactions control SNARE specificity in vivo.
结合相互作用控制体内 SNARE 特异性。
DOI: 10.1083/jcb.200809178
发表时间: 2008
期刊: The Journal of cell biology
影响因子: --
作者: [Yang,Hui-Ju, Nakanishi,Hideki, Liu,Song, McNew,JamesA, Neiman,AaronM]
通讯作者: Neiman,AaronM
DOI: 10.1083/jcb.200107008
发表时间: 2001-11-26
期刊: The Journal of cell biology
影响因子: --
作者: [Tachikawa H, Bloecher A, Tatchell K, Neiman AM]
通讯作者: Neiman AM
Mechanisms of de novo membrane assembly
INTERACTIONS BETWEEN PROTEINS OF THE MEIOTIC SPINDLE POLE BODY
  • 批准号:
    8365796
  • 项目类别:
  • 资助金额:
    $2.88万
  • 财政年份:
    2011
  • 负责人:
    Aaron M Neiman
  • 依托单位:
Chromatin and the Control of Late Meiotic Gene Expression
TRAINING IN LIVE CELL FLUORESCENCE MICROSCOPY AND FRET ANALYSIS
  • 批准号:
    7957817
  • 项目类别:
  • 资助金额:
    $0.68万
  • 财政年份:
    2009
  • 负责人:
    Aaron M Neiman
  • 依托单位:
国内基金
海外基金
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
  • 批准号:
    32170319
  • 项目类别:
    面上项目
  • 资助金额:
    58.00万元
  • 批准年份:
    2021
  • 负责人:
    董春海
  • 依托单位:
帽结合蛋白(cap binding protein)调控乙烯信号转导的分子机制
  • 批准号:
    --
  • 项目类别:
    --
  • 资助金额:
    58万元
  • 批准年份:
    2021
  • 负责人:
    董春海
  • 依托单位:
ID1 (Inhibitor of DNA binding 1) 在口蹄疫病毒感染中作用机制的研究
番茄EIN3-binding F-box蛋白2超表达诱导单性结实和果实成熟异常的机制研究
  • 批准号:
    31372080
  • 项目类别:
    面上项目
  • 资助金额:
    80.0万元
  • 批准年份:
    2013
  • 负责人:
    杨迎伍
  • 依托单位: