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DESCRIPTION (provided by applicant): The baculoviruses are large DNA viruses distinguished by their prolific multiplication in host insects. Due to their unique properties, these pathogens are used as vectors for foreign gene expression, potent biological insecticides, and gene transfer vehicles. To ensure their replicative success, baculoviruses use novel mechanisms that expedite viral gene expression and suppress host defenses, including cell death by apoptosis. It is the long term goal of this project to investigate the molecular interactions between baculoviruses and their host cell by defining the mechanisms by which Autographa californica nucleopolyhedrovirus (AcMNPV) regulates gene expression and modulates the host apoptotic response. In an integrated series of experiments that use biochemical, genetic, and cell biology approaches, the molecular mechanisms by which early AcMNPV transcriptional regulators accelerate replication will be investigated. The mechanism of enhancer-mediated transcriptional activation by the immediate early transregulator IE1 will be determined by using new loss-of-function mutations and dominant inhibitors. These dominant inhibitors will be used in combination with interfering RNA (RNAi) to define the roles of IE1 during infection, including the induction of apoptosis. AcMNPV-infected insect cells will be used as a powerful yet convenient system to define the molecular signals by which DNA viruses trigger apoptosis. Capitalizing on the finding that AcMNPV induces widespread apoptosis in cultured Drosophila melanogaster cells, we use dominant inhibitors, RNAi, and the baculovirus apoptotic suppressors (p35, p49, and iap) to investigate the viral and cellular apoptotic factors in this model organism for which many of the cell death components are known. These studies will be complemented by a characterization of the molecular signals (viral and host) responsible for nodavirus-induced apoptosis in Drosophila. Collectively, these studies are expected to provide important insight into the highly conserved pathways of apoptosis, which contribute significantly to the pathogenicity of human viruses. In addition, the molecular mechanisms by which baculoviruses regulate early gene transcription are directly relevant to insect vectors of human disease.
期刊论文(30)
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The 35-kilodalton protein gene (p35) of Autographa californica nuclear polyhedrosis virus and the neomycin resistance gene provide dominant selection of recombinant baculoviruses.
苜蓿银纹夜蛾核多角体病毒的 35 千道尔顿蛋白基因 (p35) 和新霉素抗性基因提供了重组杆状病毒的显性选择。
DOI: 10.1093/nar/21.8.1753
发表时间: 1993
期刊: Nucleic acids research
影响因子: 14.9
作者: [Lerch,RA, Friesen,PD]
通讯作者: Friesen,PD
The baculovirus-integrated retrotransposon TED encodes gag and pol proteins that assemble into viruslike particles with reverse transcriptase.
杆状病毒整合的逆转录转座子 TED 编码 gag 和 pol 蛋白,这些蛋白通过逆转录酶组装成病毒样颗粒。
DOI: 10.1128/jvi.66.3.1590-1601.1992
发表时间: 1992
期刊: Journal of virology
影响因子: 5.4
作者: [Lerch,RA, Friesen,PD]
通讯作者: Friesen,PD
The Env-like open reading frame of the baculovirus-integrated retrotransposon TED encodes a retrovirus-like envelope protein.
杆状病毒整合的逆转录转座子 TED 的类 Env 开放阅读框编码一种类逆转录病毒包膜蛋白。
DOI: 10.1006/viro.1996.0653
发表时间: 1996
期刊: Virology.
影响因子: --
作者: [Ozers,MS, Friesen,PD]
通讯作者: Friesen,PD
Proteolytic processing and assembly of gag and gag-pol proteins of TED, a baculovirus-associated retrotransposon of the gypsy family.
TED 的 gag 和 gag-pol 蛋白的蛋白水解加工和组装,TED 是吉普赛家族的杆状病毒相关逆转录转座子。
DOI: 10.1128/jvi.72.11.8718-8724.1998
发表时间: 1998
期刊: Journal of virology
影响因子: 5.4
作者: [Hajek,KL, Friesen,PD]
通讯作者: Friesen,PD
REGULATION OF VIRUS-INDUCED PROGRAMMED CELL DEATH
  • 批准号:
    7061620
  • 项目类别:
  • 资助金额:
    $24.6万
  • 财政年份:
    1997
  • 负责人:
    PAUL D FRIESEN
  • 依托单位:
REGULATION OF VIRUS INDUCED PROGRAMMED CELL DEATH
  • 批准号:
    6341661
  • 项目类别:
  • 资助金额:
    $20.37万
  • 财政年份:
    1997
  • 负责人:
    PAUL D FRIESEN
  • 依托单位:
REGULATION OF VIRUS-INDUCED PROGRAMMED CELL DEATH
  • 批准号:
    6835707
  • 项目类别:
  • 资助金额:
    $25.2万
  • 财政年份:
    1997
  • 负责人:
    PAUL D FRIESEN
  • 依托单位:
REGULATION OF VIRUS INDUCED PROGRAMMED CELL DEATH
  • 批准号:
    2856049
  • 项目类别:
  • 资助金额:
    $19.21万
  • 财政年份:
    1997
  • 负责人:
    PAUL D FRIESEN
  • 依托单位:
国内基金
海外基金
Epac1/2通过蛋白酶体调控中性粒细胞NETosis和Apoptosis在急性肺损伤中的作用研究
  • 批准号:
    LBY21H010001
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2020
  • 负责人:
    郑绪阳
  • 依托单位:
基于Apoptosis/Ferroptosis双重激活效应的天然产物AlbiziabiosideA的抗肿瘤作用机制研究及其结构改造
  • 批准号:
    81703335
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2017
  • 负责人:
    卫高菲
  • 依托单位:
双肝移植后Apoptosis和pyroptosis在移植物萎缩差异中的作用和供受者免疫微环境变化研究
  • 批准号:
    81670594
  • 项目类别:
    面上项目
  • 资助金额:
    58.0万元
  • 批准年份:
    2016
  • 负责人:
    陈昊
  • 依托单位:
Serp-2 调控apoptosis和pyroptosis 对肝脏缺血再灌注损伤的保护作用研究
  • 批准号:
    81470791
  • 项目类别:
    面上项目
  • 资助金额:
    73.0万元
  • 批准年份:
    2014
  • 负责人:
    董家鸿
  • 依托单位: