Mechanistic Studies on Sindbis Virus Replication

辛德毕斯病毒复制机制研究

• 批准号: 0416048
• 负责人: Richard Hardy
• 金额: --
• 依托单位: Indiana University
• 依托单位国家: 美国
• 项目类别: Continuing Grant
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-09-01 至 2008-08-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=0416048&HistoricalAwards=false
• 关键词: Mechanistic; Studies; Sindbis; Virus; Replication

Positive-sense RNA viruses represent a diverse group of economically and medically important pathogens. The genomic RNA of these viruses is a multi-functional molecule that serves as an mRNA for translation of virus proteins and a template for the synthesis of a minus-sense RNA replication intermediate. In order to determine the means by which genome function is regulated this project focuses on Sindbis virus (the type species of the genus Alphavirus) minus-strand RNA synthesis programmed by the positive-sense genomic RNA and committed by the viral replicase. The long-term goal of the research is to develop an integrated model of Sindbis virus gene expression and genome replication. This project will investigate how RNA sequence elements at the 5' and 3' end of the Sindbis virus genome effect template recognition by the viral replicase, regulate template function, and facilitate productive initiation of minus-strand RNA synthesis. Using experimental systems established in the laboratory the research aims to: 1) map determinants in the 5' region of the genome and their cognate binding factors required for minus-strand RNA synthesis, and 2) elucidate the mechanism by which residues at the 3' end of the genome facilitate productive initiation of minus-strand RNA synthesis. Results from these studies will specifically impact the understanding of alphavirus gene expression and replication. Further, as single-stranded positive-sense RNA viruses are united by a common scheme of genome replication, principles established from these studies will have broader implications for this group of viruses generally. The project will involve the training of graduate students and a postdoctoral researcher. In addition, students from the university's program for underrepresented groups in the life sciences will be participants in this research project.

正义RNA病毒代表了一组经济和医学上重要的病原体。这些病毒的基因组RNA是一种多功能分子，可作为翻译病毒蛋白的mRNA和合成负义RNA复制中间体的模板。为了确定基因组功能调节的方式，该项目侧重于辛德毕斯病毒（甲病毒属的模式种）负链RNA合成，该负链RNA合成由正义基因组RNA编程并由病毒复制酶提交。该研究的长期目标是开发辛德比斯病毒基因表达和基因组复制的综合模型。本项目将研究辛德毕斯病毒基因组5'端和3'端的RNA序列元件如何影响病毒复制酶的模板识别，调节模板功能，并促进负链RNA合成的有效起始。利用实验室建立的实验系统，本研究的目的是：1）定位基因组5'区的决定簇及其负链RNA合成所需的同源结合因子，2）阐明基因组3'端残基促进负链RNA合成的有效起始的机制。这些研究的结果将特别影响对甲病毒基因表达和复制的理解。此外，由于单链正义RNA病毒通过基因组复制的共同方案结合在一起，因此从这些研究中建立的原则将对这组病毒产生更广泛的影响。 该项目将涉及培训研究生和一名博士后研究员。 此外，该大学生命科学领域代表性不足群体项目的学生将参与该研究项目。