CELLULAR SIGNALING BY DOUBLE STRANDED RNA
CELLULAR SIGNALING BY DOUBLE STRANDED RNA
批准号:
6102952
负责人:
GANES C. SEN
金额:
$23.69万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-06-01 至 2000-03-31
关键词:
RNA binding protein biological signal transduction cell cycle complementary DNA double stranded RNA gene induction /repression genetic library genetic regulation laboratory mouse molecular cloning nucleic acid metabolism protein purification protein structure function tissue /cell culture transcription factor transfection
中文摘要
本项目将研究双链(DS)RNA对细胞信号的影响。DsRNA是基因转录、蛋白质合成和细胞生长的重要调节因子。在干扰素系统的背景下,已经发现了dsRNA的多种细胞功能,该系统的不同方面将在该计划的其他项目中进行研究。DsRNA的转录信号将使用缺陷细胞突变体进行分析。一个这样的突变体已经被分离出来,在拟议的调查过程中将产生更多的突变体。突变细胞将被检查候选蛋白质中可能涉及dsRNA信号的缺陷。如果没有发现这种缺陷,将用野生型细胞构建的cDNA表达文库来补充细胞,并克隆突变的蛋白。在另外两个目标中,将研究在上一个资助期克隆的两个dsRNA结合蛋白的细胞功能。一种名为PACT的蛋白质与PKR相互作用并激活它。激活过程的机制及其对转录信号、蛋白质合成和细胞生长调节的影响将被研究。P9O是另一种dsRNA结合蛋白,是一种核磷蛋白。它可能参与细胞周期调节和核RNA代谢将被研究。这项拟议的研究将提供有关dsRNA细胞功能的重要机制信息,dsRNA是病毒感染细胞的主要调节因子。
英文摘要
Cellular signaling by double-stranded (ds) RNA will be investigated in this project. DsRNA is an important regulator of gene transcription, protein synthesis and cell growth. The multiple cellular functions of dsRNA have been discovered in the contexts of the interferon system, different aspects of which will be studied in the other projects of this program. Transcriptional signaling by dsRNA will be analyzed using defective cell mutants. One such mutant has been already isolated and more will be generated during the course of the proposed investigation. The mutant cells will be examined for defects in candidate proteins which might be involved in dsRNA signaling. If no such defect is found, the cells will be complemented with cDNA expression libraries made from wild-type cells and the mutated protein will be cloned. In two other aims, cellular functions of two dsRNA-binding proteins, which were cloned during the last funding period, will be investigated. One protein, PACT interacts with PKR and activates it. The mechanism of the activation process and its consequence on transcriptional signaling, protein synthesis and cell growth regulation will be studied. P9O, the other dsRNA-binding protein, is a nuclear phosphoprotein. Its possible involvement in cell cycle regulation and nuclear RNA metabolism will be investigated. The proposed studies will provide important mechanistic information about the cellular functions of dsRNA, a major regulator in virus-infected cells.
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