Epstein Barr virus antisense transcription
Epstein Barr virus antisense transcription
批准号:
8750146
负责人:
ERIK K FLEMINGTON
金额:
$37.63万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-02-18 至 2019-01-31
关键词:
Acquired Immunodeficiency SyndromeArchitectureB-LymphocytesCodeComplexDNADNA biosynthesisFractionationFunctional RNAGenesGenetic TranscriptionHuman Herpesvirus 4Immune systemInfectionLife Cycle StagesLymphomaMicroRNAsModelingMolecularMolecular TargetNorthern BlottingOncogenicPatientsPhasePlayProcessProductionPropertyProteinsRNARoleSignal TransductionTextureTherapeuticTimeTranscriptViralViral ProteinsVirionVirusVirus Replicationpublic health relevanceresponsetooltraffickingviron
中文摘要
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英文摘要
DESCRIPTION: Reactivation in B-cells is critical for the Epstein Barr virus (EBV) life cycle and it
plays a role in amplifying viral titers in AIDS patients. The repertoire of EBV genes thought to be
involved in viral replication consists primarily of approximately 80-90 protein-coding genes. These viral proteins play very diverse roles in virus production including roles in DNA replication, RNA transcription, molecular trafficking, virion assembly, viral egress, host shut-off etc. This is not to mention roles as viron components; both components that form the virus architecture as well as those that are involved in inducing the rapid signaling responses immediately following new infection. We hypothesize that in addition to this group of known protein coding genes, EBV encodes a previously unappreciated group of long non-coding transcripts that will ultimately be found to play an equally diverse set of functions in virus replication. Conceptually this would be important because it would change the texture and the details of how most of us visualize the reactivation process. From a practical standpoint, it would
give us a new class of molecular targets that may offer the application of alternative therapeutic approaches against EBV.
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Epstein Barr virus antisense transcription
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批准号:9206435
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财政年份:2014
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依托单位:
Intercellular communication in Epstein Barr virus reactivation
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Role of the cellular microRNA, miR-155, in EBV type III latency signaling
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海外基金