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The role of the host Ca/Mn pump in emergence of novel viral RNA recombinants

The role of the host Ca/Mn pump in emergence of novel viral RNA recombinants
宿主 Ca/Mn 泵在新型病毒 RNA 重组体中的作用
批准号:
7847640
负责人:
PETER NAGY
金额:
$20.85万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-05-22 至 2012-04-30

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DESCRIPTION (provided by applicant): Emergence of new viruses is a continuing threat to our society. Evolution of plus- stranded RNA viruses is frequently driven by RNA recombination, a process that joins noncontiguous RNA segments together, creating novel combinations of genes or regulatory RNA sequences. Recombination is important for RNA viruses to overcome immunity, jump species and change viral pathogenicity in all types of living organisms. Studies on viral RNA recombination are critical to understand the recombination process and the role of specific host genes, whose roles in the recombination process are currently unknown. The investigator will use Tomato bushy stunt virus (TBSV), which is currently the most advanced among viral systems to progress rapidly in understanding the mechanism of RNA recombination and the role of the host genes. The investigator's research opens up a completely new area with the powerful TBSV-yeast model system, which has led to genome-wide screens identifying host genes suppressing RNA recombination for the first time. Additional advantage of the similarity of TBSV replicase proteins to proteins of important pathogens, such as Hepatitis C virus (HCV), dengue virus, West Nile virus and other Flaviviruses and Pestiviruses. Collectively, the major advances with TBSV allow the investigator to conduct experiments on the roles of host factors that are currently only feasible with TBSV, but will open new approaches for studying RNA recombination/evolution for important human pathogens. This proposal focuses on one of the key host factors suppressing RNA recombination. The experiments will dissect the role of Pmr1p Ca2+/Mn2+ pump in viral RNA recombination. Pmr1p is a ubiquitous and conserved protein in eukaryotes. The human homologs of Pmr1p have been shown to play critical roles in genetic diseases, such as Hailey- Hailey Disease and Darier disease. In the absence of Pmr1p, the rate of TBSV RNA recombination is extremely high demonstrating the critical role of the host in viral RNA recombination. In order to characterize the role of Pmr1p in RNA recombination, the investigator will use the advanced genetics tools available for yeast in combination with biochemical approaches. The results obtained in cell-free systems and in yeast model host, will also be confirmed in a native plant host. In addition, in vitro experiments will be conducted with the RdRp of HCV, an important human pathogen, to expand our knowledge on the possible role of Ca2+/Mn2+ pumps in HCV RNA recombination. The following are major strengths of the proposal: (i) Viral RNA recombination is clearly of immense importance for viruses to overcome immunity, jump species and change pathogenicity in all types of living organisms. (ii) The combination of yeast and in vitro systems developed by the investigator is currently the only one in the world suitable for studying the mechanism of host factors involvement in viral RNA recombination. (iii) This research is expected to lead to groundbreaking new discoveries in viral RNA recombination. The highly tractable in vitro and in vivo TBSV system developed by the investigator could prove highly beneficial to studies of other, less amenable RNA viruses. The research holds promise of benefiting society by leading to groundbreaking results in the area of virus recombination/evolution, host-virus interaction and the emergence of new viruses. PUBLIC HEALTH RELEVANCE: Emergence of new viruses is a continuing threat to our society. New plus-stranded RNA viruses emerge frequently due to RNA recombination. Recombination is important for RNA viruses to overcome immunity, jump to new host species or change the severity of symptoms in all types of living organisms. The roles of the host in virus recombination are currently poorly understood due to the lack of tractable virus-host systems. The investigator will use Tomato bushy stunt virus (TBSV), which is currently the most advanced among viral systems to study RNA recombination and the role of the host genes. This proposal focuses on one of the key host factors suppressing RNA recombination by dissecting the role of a Ca2+/Mn2+ pump in viral RNA recombination. The research holds promise of benefiting society by leading to groundbreaking results in the area of virus recombination/evolution, host-virus interaction and the emergence of new viruses.
期刊论文(5)
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会议论文
Proteome-wide overexpression of host proteins for identification of factors affecting tombusvirus RNA replication: an inhibitory role of protein kinase C.
宿主蛋白的蛋白质组范围内过度表达,用于鉴定影响烟草病毒 RNA 复制的因素:蛋白激酶 C 的抑制作用。
DOI: 10.1128/jvi.00019-12
发表时间: 2012
期刊: Journal of virology
影响因子: 5.4
作者: [ShahNawaz-ul-Rehman,Muhammad, Martinez-Ochoa,Natalia, Pascal,Helene, Sasvari,Zsuzsanna, Herbst,Christin, Xu,Kai, Baker,Jannine, Sharma,Monika, Herbst,Alan, Nagy,PeterD]
通讯作者: Nagy,PeterD
p33-Independent activation of a truncated p92 RNA-dependent RNA polymerase of Tomato bushy stunt virus in yeast cell-free extract.
p33-酵母无细胞提取物中番茄丛状特技病毒截短的 p92 RNA 依赖性 RNA 聚合酶的独立激活。
DOI: 10.1128/jvi.01303-12
发表时间: 2012
期刊: Journal of virology
影响因子: 5.4
作者: [Pogany,Judit, Nagy,PeterD]
通讯作者: Nagy,PeterD
Authentic in vitro replication of two tombusviruses in isolated mitochondrial and endoplasmic reticulum membranes.
两种烟草病毒在分离的线粒体和内质网膜中的真实体外复制。
DOI: 10.1128/jvi.00973-12
发表时间: 2012
期刊: Journal of virology
影响因子: 5.4
作者: [Xu,Kai, Huang,Tyng-Shyan, Nagy,PeterD]
通讯作者: Nagy,PeterD
An inhibitory function of WW domain-containing host proteins in RNA virus replication.
含有 WW 结构域的宿主蛋白在 RNA 病毒复制中的抑制功能。
DOI: 10.1016/j.virol.2012.01.020
发表时间: 2012
期刊: Virology
影响因子: 3.7
作者: [Qin,Jun, Barajas,Daniel, Nagy,PeterD]
通讯作者: Nagy,PeterD
Blocking RNA virus replication through the antiviral functions of cellular helicases
  • 批准号:
    9021423
  • 项目类别:
  • 资助金额:
    $17.5万
  • 财政年份:
    2015
  • 负责人:
    PETER NAGY
  • 依托单位:
Mechanism of inhibition of RNA virus replication by host WW-domain proteins
  • 批准号:
    8624215
  • 项目类别:
  • 资助金额:
    $17.5万
  • 财政年份:
    2014
  • 负责人:
    PETER NAGY
  • 依托单位:
Mechanism of inhibition of +RNA virus replication by cyclophilins
  • 批准号:
    8179013
  • 项目类别:
  • 资助金额:
    $17.38万
  • 财政年份:
    2011
  • 负责人:
    PETER NAGY
  • 依托单位:
Mechanism of inhibition of +RNA virus replication by cyclophilins
  • 批准号:
    8279153
  • 项目类别:
  • 资助金额:
    $20.41万
  • 财政年份:
    2011
  • 负责人:
    PETER NAGY
  • 依托单位:
国内基金
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层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
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  • 项目类别:
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  • 资助金额:
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  • 批准年份:
    2021
  • 负责人:
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寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
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    32001603
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2020
  • 负责人:
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AREA国际经济模型的移植.改进和应用
  • 批准号:
    18870435
  • 项目类别:
    面上项目
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    2.0万元
  • 批准年份:
    1988
  • 负责人:
    史树中
  • 依托单位: