Viral and cellular gene regulation during lytic KSHV replication
Viral and cellular gene regulation during lytic KSHV replication
批准号:
7175485
负责人:
Sankar Swaminathan
金额:
$22.38万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-02-03 至 2010-12-31
关键词:
Acquired Immunodeficiency SyndromeAffectAntiviral AgentsAreaB-LymphocytesBindingBiologicalBiologyCellsDevelopmentEndothelial CellsFamilyGene ActivationGene ExpressionGene Expression RegulationGenesGoalsHIVHIV InfectionsHerpesviridaeHomologous GeneHomologous ProteinHumanHuman Herpesvirus 4Human Herpesvirus 8Human herpesvirus 4 SM proteinImmune responseImmune systemIndividualInfectionIntronsKaposi SarcomaKnowledgeLife Cycle StagesLinkLymphocyteLymphomaLyticMalignant NeoplasmsMediatingMessenger RNAMolecularMolecular GeneticsMorbidity - disease rateMulticentric Angiofollicular Lymphoid HyperplasiaNuclear ExportPathogenesisPharmaceutical PreparationsPhenotypePlayProcessProliferatingPropertyProteinsRNA ProcessingRateRecombinantsRepressionRoleSimplexvirusSpecificityTestingTranscriptViralViral ProteinsVirusVirus Replicationbasecellular targetingeffusiongenetic regulatory proteinimmunosuppressedinsightlytic gene expressionlytic replicationmRNA Exportmembermortalitymutantneoplastic cellnovelpathogenpreventprotein functiontherapeutic targettumortumorigenesis
中文摘要
描述(由申请人提供):本申请的广泛、长期目标是了解卡波西肉瘤相关疱疹病毒(KSHV/HHV-8)的调节蛋白如何在裂解复制期间控制病毒和细胞基因表达。裂解基因产物可能在KSHV的发病机制中起作用,有助于KSHV感染细胞和邻近细胞增殖、存活和避免免疫应答的能力。因此,了解裂解基因表达的调节机制与KSHV相关的发病机制有关,KSHV相关的发病机制仍然是发病率和死亡率的重要原因,特别是在HIV和KSHV感染流行率高的地区。KSHV的ORF 57蛋白在KSHV复制期间早期表达,并且是在疱疹病毒复制中起重要作用的疱疹病毒蛋白家族的成员。ORF 57具有独特的调控特性,在转录后增强许多无内含子基因的表达。此外,ORF 57增强特定细胞基因的表达。ORF 57可能通过与mRNA物理结合并调节其稳定性和核输出来发挥其许多作用。关于ORF 57影响RNA加工的机制以及如何确定其作用的特异性仍然未知。因此,我们提出了三个综合的目标,调查的作用,ORF 57在KSHV生物学。在第一个目标中,我们将定义ORF 57结合mRNA的机制以及ORF 57特异性是如何确定的。在第二个目标中,我们将确定对ORF 57功能重要的主要细胞蛋白,特别是关于核输出和mRNA加工。在第三个目标中,我们将使用分子遗传学确定ORF 57的哪些功能对于KSHV复制是必不可少的。我们还将确定ORF 57对内皮细胞和B淋巴细胞中基因表达的特异性影响。KSHV是一种与癌症发展有关的病毒,特别是在那些免疫系统较弱的人中,如艾滋病毒感染者。研究病毒如何繁殖对于了解它如何影响它感染的细胞并将其转化为肿瘤细胞非常重要。这些研究也有可能确定针对病毒的新药的靶点,这可能有助于预防或治疗感染。
英文摘要
DESCRIPTION (provided by applicant): The broad, long term objective of this application is to understand how regulatory proteins of Kaposi's sarcoma-associated herpesvirus (KSHV/HHV-8) control viral and cellular gene expression during lytic replication. Lytic gene products are likely to have a role in pathogenesis of KSHV, contributing to the ability of KSHV-infected cells and adjacent cells to proliferate, survive and avoid immune responses. Understanding the mechanisms by which lytic gene expression is regulated is therefore relevant to KSHV- related pathogenesis which continues to be a significant cause of morbidity and mortality, particularly in areas with high endemic rates of HIV and KSHV infection. The ORF57 protein of KSHV is expressed early during KSHV replication and is a member of a family of herpesvirus proteins that plays an essential role in herpesvirus replication. ORF57 has unique regulatory properties, post-transcriptionally enhancing expression of many intronless genes. In addition, ORF57 enhances expression of specific cell genes. ORF57 is likely to exert many of its effects by physically binding to mRNA and modulating its stability and nuclear export. Much remains unknown about the mechanisms by which ORF57 affects RNA processing and how its specificity of action is determined. We therefore propose three integrated aims to investigate the role of ORF57 in KSHV biology. In the first aim, we will define the mechanisms by which ORF57 binds mRNA and how ORF57 specificity is determined. In the second aim, we will identify the major cellular proteins that are important for ORF57 function, especially with regard to nuclear export and mRNA processing. In the third aim, we will determine which functions of ORF57 are essential for KSHV replication using molecular genetics. We will also determine the specific effects of ORF57 on gene expression in endothelial cells and B lymphocytes. KSHV is a virus that is linked to the development of cancer, particularly in those people who have weakened immune systems, such as those with HIV infection. Studying how the virus reproduces is important to understand how it affects the cells it infects and converts them to tumor cells. Such studies also have the potential to identify targets for new drugs against the virus that may help prevent or treat infection.
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会议论文
Restriction of Oncogenic Herpesviruses by Host Cell Factors
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批准号:9794739
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项目类别:
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资助金额:$0.0万
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财政年份:2014
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负责人:Sankar Swaminathan
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依托单位:
Restriction of Oncogenic Herpesviruses by Host Cell Factors
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批准号:9275403
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资助金额:$0.0万
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财政年份:2014
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负责人:Sankar Swaminathan
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依托单位:
Restriction of Oncogenic Herpesviruses by Host Cell Factors
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批准号:8966542
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项目类别:
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资助金额:$0.0万
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财政年份:2014
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负责人:Sankar Swaminathan
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依托单位:
Viral and cellular gene regulation during lytic KSHV replication
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批准号:7064117
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项目类别:
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资助金额:$24.22万
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财政年份:2006
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负责人:Sankar Swaminathan
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依托单位:
Viral and cellular gene regulation during lytic KSHV replication
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批准号:7751310
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项目类别:
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资助金额:$4.52万
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财政年份:2006
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负责人:Sankar Swaminathan
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依托单位:
Viral and cellular gene regulation during lytic KSHV replication
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批准号:8218705
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项目类别:
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资助金额:$18.31万
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财政年份:2006
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负责人:Sankar Swaminathan
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依托单位:
Viral and cellular gene regulation during lytic KSHV replication
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批准号:7343176
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资助金额:$22.35万
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财政年份:2006
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负责人:Sankar Swaminathan
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依托单位:
Viral and cellular gene regulation during lytic KSHV replication
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批准号:7538417
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项目类别:
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资助金额:$22.32万
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财政年份:2006
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负责人:Sankar Swaminathan
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依托单位:
SUBPROJECT 2
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批准号:7092453
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项目类别:
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资助金额:$69.71万
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财政年份:2005
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负责人:Sankar Swaminathan
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依托单位:
POSTTRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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批准号:6350367
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资助金额:$22.19万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
POSTTRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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批准号:2829852
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项目类别:
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资助金额:$19.89万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
Post-transcriptional Gene Regulation by EBV SM Protein
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批准号:7069622
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项目类别:
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资助金额:$25.57万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
Post-transcriptional Gene Regulation by EBV SM Protein
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批准号:6798986
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资助金额:$26.18万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
POST-TRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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批准号:8444347
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项目类别:
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资助金额:$23.93万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
POST-TRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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批准号:8230477
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资助金额:$25.52万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
Post-transcriptional Gene Regulation by EBV SM Protein
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资助金额:$24.83万
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POSTTRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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负责人:Sankar Swaminathan
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依托单位:
REGULATION OF ANGIOGENESIS BY HUMAN HERPESVIRUS 8
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资助金额:$14.1万
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财政年份:1999
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负责人:Sankar Swaminathan
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POST-TRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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项目类别:
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资助金额:$24.67万
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财政年份:1999
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负责人:Sankar Swaminathan
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依托单位:
POST-TRANSCRIPTIONAL GENE REGULATION BY EBV SM PROTEIN
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项目类别:
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资助金额:$25.57万
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财政年份:1999
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依托单位:
海外基金