Role of NEAT1 lncRNA in HIV replication
Role of NEAT1 lncRNA in HIV replication
批准号:
9292251
负责人:
Andrew P Rice
金额:
$19.81万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-06-09 至 2018-05-31
关键词:
AddressAffectBiologyCCL19 geneCD4 Positive T LymphocytesCell NucleusCell modelCellsChromatinCytoplasmDataElementsGene ExpressionGene Expression RegulationGenesGenetic TranscriptionGenomeHIVHIV InfectionsHumanLengthMaintenanceMapsMediatingMemoryNuclearNuclear ExportNuclear StructurePatternPlayPoly APropertyProteinsProvirusesRNARNA Polymerase IIRNA SplicingRepressionResearchRestRoleSiteSmall Interfering RNASpicesT-Cell ActivationT-LymphocyteTestingTranscriptTranscription Initiation SiteUntranslated RNAUntranslated RegionsViralVirus Latencychromatin remodelinginnovationinsightlatent infectionmRNA Precursormemory CD4 T lymphocytenovelpromoterrev Proteinscaffoldtranscription terminationviral RNA
中文摘要
NEAT1_1和NEAT1_2是相关的长非编码RNA(lncRNA),其在细胞中积累到高水平。
原子核NEAT 1 RNA作为组装称为paraspeckles的核结构的基本支架,
除了lncRNA外还含有大约45种蛋白质。最近的研究结果表明,不完全
剪接的HIV RNA通过与旁斑的结合保留在细胞核中。重要的是,NEAT1
RNA在静息的CD4 T细胞中以高水平表达,并且它们的水平被T细胞免疫抑制剂强烈下调。
activation.这种表达模式表明NEAT 1 RNA的功能是将病毒转录物保留在细胞中。
静止的CD4 T细胞的细胞核。这项拟议中的研究将调查病毒的核滞留是否
NEAT1 RNA的作用是抑制HIV在静息CD4 T细胞中的复制,以及维持HIV
静息CD4 T细胞的潜伏期。此外,旁斑蛋白包括几种RNA剪接因子,
染色质重塑蛋白。因此,该研究还将研究NEAT1 RNA是否在HIV中发挥作用
通过RNA聚合酶II进行RNA剪接和前病毒转录。完成拟议的研究可能会
为HIV基因调控和病毒潜伏机制提供了新的见解。
英文摘要
NEAT1_1 and NEAT1_2 are related long noncoding RNAs (lncRNAs) that accumulate to high levels in the
nucleus. NEAT1 RNAs serve as essential scaffolds to assemble nuclear structures termed paraspeckles that
contain approximately 45 proteins in addition to the lncRNAs. Recent findings indicate that incompletely
spliced HIV RNAs are retained in the nucleus through an association with paraspeckles. Importantly, NEAT1
RNAs are expressed at high levels in resting CD4 T cells, and their levels are strongly down-regulated by T cell
activation. This expression pattern suggests that NEAT1 RNAs function to retain viral transcripts in the
nucleus of quiescent CD4 T cells. The proposed research will investigate whether the nuclear retention of viral
RNAs by NEAT1 RNAs acts to repress HIV replication in resting CD4 T cells, as well as to maintain HIV
latency in resting CD4 T cells. Additionally, paraspeckle proteins include several RNA splicing factors and
chromatin remodeling proteins. The research will therefore also examine if NEAT1 RNAs play roles in HIV
RNA splicing and proviral transcription by RNA Polymerase II. Completion of the proposed research is likely to
provide new insight into mechanisms of HIV gene regulation and viral latency.
期刊论文(1)
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科研奖励(0)
会议论文
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批准号:10609476
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财政年份:2014
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P-TEFb and HIV Latency
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批准号:8505377
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财政年份:2012
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批准号:8401302
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资助金额:$23.48万
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财政年份:2012
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财政年份:2010
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依托单位:
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Structure and function of influenza A virus PDZ-binding motif
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资助金额:$19.0万
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财政年份:2010
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依托单位:
Effects of cocaine on miRNAs that regulate HIV-1 replication
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项目类别:
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资助金额:$29.17万
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财政年份:2010
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负责人:Andrew P Rice
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依托单位:
Structure and function of influenza A virus PDZ-binding motif
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批准号:7989324
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项目类别:
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资助金额:$23.03万
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财政年份:2010
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负责人:Andrew P Rice
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依托单位:
Virology Core
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批准号:7929999
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项目类别:
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负责人:Andrew P Rice
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依托单位:
Identification of novel HIV-1 co-factors
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批准号:7767655
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项目类别:
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资助金额:$19.0万
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财政年份:2009
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负责人:Andrew P Rice
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Identification of novel HIV-1 co-factors
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项目类别:
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资助金额:$23.03万
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财政年份:2009
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负责人:Andrew P Rice
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依托单位:
Virology Core
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批准号:7683339
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项目类别:
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依托单位:
海外基金