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The role of DNA repair in retroviral infection

DNA修复在逆转录病毒感染中的作用

基本信息

批准号：
7847567
负责人：
Richard Fishel
金额：
$ 18.75万
依托单位：
OHIO STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-05-22 至 2012-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7847567
关键词：
ATP phosphohydrolase Affect Anti-Retroviral Agents Base Excision Repairs Biochemical Cell Line Cells Complementary DNA Complex Consensus Cytomegalovirus DNA Damage DNA Repair DNA Repair Pathway Degradation Pathway ERCC3 gene Elements Excision Repair Family Foundations Frequencies Future Genes Genetic Genetic Transcription Goals HIV Homologous Gene Host Defense In Vitro Infection Kinetics Lead Life Cycle Stages Measures Mediating Metabolism Mutation Nucleotide Excision Repair Oxidants Pathway interactions Phosphorylation Play Process Proteins Proviruses Public Health Retrotransposon Retroviridae Reverse Transcription Role Site Staging Transcript UV Radiation Exposure Viral Yeasts base helicase improved in vivo mutant novel potassium bromate public health relevance retroviral-mediated transcription factor TFIIH transduction efficiency

项目摘要

DESCRIPTION (provided by applicant): The Role of DNA Repair in Retroviral Infection The goal of this proposal is to examine two well-defined host DNA repair pathways that act as positive and negative regulators of retroviral infection. Our previous studies have identified the Nucleotide Excision Repair (NER) genes XPB(ERCC3) and XPD(ERCC2) as central players in a major retroviral cDNA degradation pathway that eliminates a substantial portion of the incoming cDNAs, and is responsible for significantly reducing the frequency of integration (negative retrovirus regulators). In more recent studies we have identified Base Excision Repair (BER) pathway genes that significantly enhance the efficiency of integration (positive retrovirus regulators). Both DNA repair pathways affect the retroviral life cycle at the relatively unexplored stages following reverse transcription and through completion of integration. We propose to examine the regulatory mechanisms of these two DNA repair pathways on retroviral infection with the following two specific aims: 1.) to define the components and mechanism of TFIIH mediated retroviral cDNA degradation pathway, and 2.) to elucidate the role of BER proteins on retroviral integration. These aims will be accomplished using experimental strategies that include both genetic and biochemical approaches. Understanding the mechanisms of these positive and negative regulators of retroviral infection may be the foundation for future anti-retroviral therapies. PUBLIC HEALTH RELEVANCE: Retroviruses, including HIV and the family of HTLV retroviruses, present a significant and continuing threat to public health. These studies aim at elucidating both an innate intracellular host defense against retroviral infection and a pathway of host proteins required for efficient retroviral infection. Both pathways appear to possess the potential to be exploited as targets for future novel anti-retroviral therapies.

描述（由申请人提供）：DNA修复在逆转录病毒感染中的作用本提案的目标是检查两个明确的宿主DNA修复途径，它们作为逆转录病毒感染的正调节剂和负调节剂。我们以前的研究已经确定了核苷酸切除修复（NER）基因XPB（ERCC 3）和XPD（ERCC 2）作为主要逆转录病毒cDNA降解途径中的核心参与者，该途径消除了大部分传入的cDNA，并负责显著降低整合频率（负逆转录病毒调节因子）。在最近的研究中，我们已经确定了碱基切除修复（BER）途径基因，显着提高整合效率（正逆转录病毒调节因子）。这两种DNA修复途径在逆转录后相对未被探索的阶段和通过整合完成影响逆转录病毒的生命周期。我们建议研究这两种DNA修复途径对逆转录病毒感染的调控机制，具体目标有以下两个：1）。明确TFIIH介导的逆转录病毒cDNA降解途径的组成和机制;阐明BER蛋白在逆转录病毒整合中的作用。这些目标将使用实验策略，包括遗传和生物化学方法来实现。了解这些逆转录病毒感染的积极和消极调节机制可能是未来抗逆转录病毒疗法的基础。公共卫生关系：逆转录病毒，包括HIV和HTLV逆转录病毒家族，对公众健康构成重大和持续的威胁。这些研究旨在阐明宿主对逆转录病毒感染的固有细胞内防御和有效逆转录病毒感染所需的宿主蛋白质途径。这两种途径似乎都有潜力被开发为未来新型抗逆转录病毒疗法的目标。