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中文摘要
翻译
含有双链RNA结合基序(dsRBM)的蛋白质在原核生物和真核生物中都起着关键的调节作用。该结构域与结构rna结合并参与蛋白质与蛋白质的相互作用。rna依赖性蛋白激酶(PKR)和核因子90 (NF90)各含有两个dsrbm。PKR是一种由干扰素诱导的细胞蛋白激酶,调节蛋白质合成和信号转导途径,参与病毒感染和细胞生长控制。因此,PKR受到严格调控,并接收来自各种来源的信号。NF90的几种亚型存在于细胞中,包括
英文摘要
Proteins containing the double-stranded RNA binding motif (dsRBM) play key regulatory roles in both prokaryotic and eukaryotic organisms. This domain binds to structured RNAs and participates in protein-protein interactions. The RNA-dependent protein kinase (PKR) and nuclear factor 90 (NF90) each contain two dsRBMs. PKR is a cellular protein kinase that is induced by interferon and regulates protein synthesis and signal transduction pathways involved in viral infection and cellular growth control. Accordingly, PKR is tightly regulated and receives signals from a variety of sources. Several isoforms of NF90 exist in cells, including the C-terminal variant NF110, and members of this protein family have been implicated as both regulators and substrates of PKR. The NF90 family proteins are heavily phosphorylated during mitosis and have been associated with the regulation of gene expression at several levels including transcription, translation, and RNA turnover. NF90 purifies as a heterodimer with nuclear factor 45 (NF45), which can also modulate the functions of both PKR and NF90. The overall objectives of this application are to develop an understanding of the structure and function of proteins in the NF90 family, to elucidate the functional relationships between NF90/110, NF45 and PKR, and to explore the role(s) of NF90 family proteins in virus-infected and normal cells. To these ends, we will use current technologies including mass spectrometry and RNA interference, to examine the following: 1. The regulation of PKR by NF90/110 and NF45 in human cells and the yeast model system. 2. The role of NF90/110 phosphorylation by PKR and in mitosis. 3. Protein complexes formed by NF90 isoforms and the changes brought about by viral infection, interferon treatment, and cell cycle block. 4. The functions of NF90 isoforms during infection with adenovirus and HIV.
期刊论文(35)
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会议论文
Novel rapidly evolving hominid RNAs bind nuclear factor 90 and display tissue-restricted distribution.
迅速发展的人类RNA结合核因子90并显示组织限制的分布。
DOI: 10.1093/nar/gkm668
发表时间: 2007
期刊: NUCLEIC ACIDS RESEARCH
影响因子: 14.9
作者: [Parrott, Andrew M, Mathews, Michael B]
通讯作者: Mathews, Michael B
Functional cloning of genes encoding dsRNA binding proteins.
编码 dsRNA 结合蛋白的基因的功能克隆。
DOI: 10.1016/s1046-2023(03)00054-9
发表时间: 2003
期刊: Methods (San Diego, Calif.)
影响因子: --
作者: [Ramanathan,Y, Song,Liting, Mathews,MichaelB, Tolias,PeterP]
通讯作者: Tolias,PeterP
DOI: 10.1371/journal.pone.0074414
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Hanauske-Abel HM, Saxena D, Palumbo PE, Hanauske AR, Luchessi AD, Cambiaghi TD, Hoque M, Spino M, D'Alliessi Gandolfi D, Heller DS, Singh S, Park MH, Cracchiolo BM, Tricta F, Connelly J, Popowicz AM, Cone RA, Holland B, Pe'ery T, Mathews MB]
通讯作者: Mathews MB
Cellular mRNA activates transcription elongation by displacing 7SK RNA.
细胞 mRNA 通过取代 7SK RNA 激活转录延伸。
DOI: 10.1371/journal.pone.0001010
发表时间: 2007
期刊: PloS one
影响因子: 3.7
作者: [Young,TaraM, Tsai,Michael, Tian,Bin, Mathews,MichaelB, Pe'ery,Tsafi]
通讯作者: Pe'ery,Tsafi
共 17 条
    Structured RNAs Binding to Proteins Containing the dsRBD
    • 批准号:
      8536346
    • 项目类别:
    • 资助金额:
      $23.85万
    • 财政年份:
      2012
    • 负责人:
      Michael B Mathews
    • 依托单位:
    Structured RNAs Binding to Proteins Containing the dsRBD
    Integrated LC/MS/MS System
    TRANSCRIPTION ACTIVATION OF HIV 1
    • 批准号:
      2292170
    • 项目类别:
    • 资助金额:
      $3.38万
    • 财政年份:
      1994
    • 负责人:
      Michael B Mathews
    • 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: