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Herpesviruses replicate and packagetheir genomes in the cell nucleus. In order to begin its processof escape from the cell, the virus must pass through the nuclear membrane by first budding into the inner nuclear membrane in a process called primary envelopment. The mechanism of herpesvirus envelopment is significant to human health from two points of view. First, this process represents an attractive target for therapy in that it is dissimilar in many waysto any normal cellular process, essential to the virus, and common to all herpesviruses. Second, the envelopment machinery alters the organization of the nucler anvelope and provides a usefultool for studying that organization. The research proposed here builds on our studies of herpes simplex virus UL34, an essential component of the envelopment apparatus. Results from our initialperiod of funding suggest that this protein plays critical roles inat least three aspects of envelopment including (i) Recruitment of viral proteins to the nuclear envelope, (ii)dispersal of nuclear envelope components that prevent access of the capsid to the nuclear membrane, and (iii)wrapping of the nucleocapsid in the nuclear membrane. The specific goals of the proposed research are threefold 1. We will define essential functions of the UL34 protein by characterizing a set of seven non-functional mutant UL34 proteins already in hand, and others that we will generate by mutagenesis of conserved residues, for their~ability1o perform various functions required for envelopment. 2. We will characterize critical interactions between the UL34 protein and other viral proteins involved in envelopment. This will include experiments to test the hypothesis that UL34 mediates membrane wrapping of the capsid, and a screen for interactions of UL34 with other viral proteins that may participate in envelopment. 3. We will fully characterize changes in the host cell nuclear lamina associated with infection and determine the mechanism by which UL34 and other viral proteins accomplish those changes.
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会议论文
Intragenic and extragenic suppression of a mutation in herpes simplex virus 1 UL34 that affects both nuclear envelope targeting and membrane budding.
单纯疱疹病毒 1 UL34 突变的基因内和基因外抑制,该突变影响核膜靶向和膜出芽。
DOI: 10.1128/jvi.05730-11
发表时间: 2011
期刊: Journal of virology
影响因子: 5.4
作者: [Roller,RichardJ, Haugo,AlisonC, Kopping,NoraJ]
通讯作者: Kopping,NoraJ
HSV/VZV chimeric viruses for identifying critical virus herpesvirus assembly interactions
  • 批准号:
    10442813
  • 项目类别:
  • 资助金额:
    $50.97万
  • 财政年份:
    2022
  • 负责人:
    RICHARD J ROLLER
  • 依托单位:
HSV/VZV chimeric viruses for identifying critical virus herpesvirus assembly interactions
  • 批准号:
    10556366
  • 项目类别:
  • 资助金额:
    $50.97万
  • 财政年份:
    2022
  • 负责人:
    RICHARD J ROLLER
  • 依托单位:
Characterization of the herpes simplex virus cytoplasmic assembly center in neuronal cells
  • 批准号:
    10038761
  • 项目类别:
  • 资助金额:
    $23.18万
  • 财政年份:
    2020
  • 负责人:
    RICHARD J ROLLER
  • 依托单位:
Mechanism and regulation of protein kinase functions in HSV nuclear egress
  • 批准号:
    10088400
  • 项目类别:
  • 资助金额:
    $19.31万
  • 财政年份:
    2020
  • 负责人:
    RICHARD J ROLLER
  • 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: