INHIBITION OF HOST-CELL TRANSCRIPTION BY POLIOVIRUS
INHIBITION OF HOST-CELL TRANSCRIPTION BY POLIOVIRUS
批准号:
3141675
负责人:
ASIM DASGUPTA
金额:
$18.52万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-02-01 至 1994-01-31
关键词:
DNA binding protein DNA directed RNA polymerase DNA footprinting affinity chromatography gel mobility shift assay genetic promoter element genetic transcription host organism interaction laboratory mouse mutant nucleic acid sequence poliomyelitis poliovirus tissue /cell culture transcription factor virus RNA virus cytopathogenic effect virus genetics virus infection mechanism
中文摘要
这项提案的长期目标是确定如何
脊髓灰质炎病毒抑制宿主细胞RNA合成的启动
(转录)通过RNA聚合酶II和III。与
未感染的提取物,脊髓灰质炎病毒感染的细胞提取物无法
专门转录含有polII-和的DNA模板
PolIII--推动者。补充受感染的细胞提取物,
与部分纯化的polII转录因子TFIIIC(其
与tRNA和VA1基因的内部启动子元件相互作用)
专门恢复polIII-和polIII-的转录
分别在这些转录恢复因子中的启动子
与已知的polIII和polIII转录因子结合。
转录因子活性抑制的机制(S)
病毒感染将通过比较数量进行检查,
它们的特定活动和翻译后修饰
用生化方法研究病毒感染细胞与模拟感染细胞中的因子
和血清学技术。特异性启动子结合能力
从模拟和病毒感染的细胞中分离出来的这些因素将
通过足迹和凝胶延迟分析进行分析。
我们将从感染的病毒中分离出病毒编码或诱导抑制物(S)
细胞提取物,能够抑制体外转录
使用各种生化技术的模拟感染提取物和
研究抑制物如何影响转录活性
体外因素。可能存在缺陷的突变脊髓灰质炎病毒
宿主细胞转录抑制,将用于进一步检测
抑制宿主细胞转录的机制。
阐明脊髓灰质炎病毒的负面影响机制
细胞转录因子的活性无疑会
促进更好地理解对
真核细胞中的转录。
英文摘要
The long term objective of this proposal is to determine how
poliovirus inhibits initiation of host cell RNA synthesis
(transcription)by RNA polymerases II and III. In contrast with
uninfected extracts, poliovirus-infected cell extracts are unable
to transcribe specifically DNA templates containing polII-and
polIII-promoters. Supplementation of the infected cell extracts,
with partially purified polII-transcription factor TFIIIC (which
interacts with internal promoter elements of tRNA and VA1 genes)
specifically restore transcription from polIII-and polIII-
promoters, respectively in these transcription-restoration factors
with known polIII and polIII -transcription factors.
The mechanism(s) of inhibition of transcription factor activities
by virus-infection will be examined by comparing the quantity,
specific activity and posttranslational modifications of these
factors in virus-infected vs. mock-infected cells using biochemical
and serological techniques. Specific promoter-binding abilities
of these factors isolated form mock-and virus-infected cells will
be analyzed by footprinting and gel-retardation assays.
We will isolate virus-encoded or -induced inhibitor(S)from infected
cell extracts, capable of inhibiting in vitro transcription in
mock-infected extracts using various biochemical techniques and
examine how the inhibitor affects activities of transcription
factors in vitro. Mutant polioviruses which may be defective in
host cell transcription-inhibition, will be used to further examine
the mechanism of inhibition of host cell transcription.
Elucidation of the mechanism by which poliovirus negatively affects
cellular transcription factor activities would undoubtedly
facilitate a better understanding of the regulation of
transcription in eukaryotic cells.
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会议论文
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依托单位:
PICORNAVIRUS TRANSLATION/INHIBITION BY SMALL YEAST RNA
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依托单位:
海外基金