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本文引用的文献

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KSHV Rta Promoter Specification and Viral Reactivation.卡波西肉瘤相关疱疹病毒Rta启动子的特异性与病毒激活
Front Microbiol. 2012 Feb 14;3:30. doi: 10.3389/fmicb.2012.00030. eCollection 2012.
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Small open reading frames: current prediction techniques and future prospect.小开放阅读框:当前的预测技术和未来展望。
Curr Protein Pept Sci. 2011 Sep;12(6):503-7. doi: 10.2174/138920311796957667.
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A large intergenic noncoding RNA induced by p53 mediates global gene repression in the p53 response.p53 诱导的一个大型基因间非编码 RNA 介导 p53 应答中的全基因组基因沉默。
Cell. 2010 Aug 6;142(3):409-19. doi: 10.1016/j.cell.2010.06.040.
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Small peptides switch the transcriptional activity of Shavenbaby during Drosophila embryogenesis.小分子肽在果蝇胚胎发生过程中改变 Shavenbaby 的转录活性。
Science. 2010 Jul 16;329(5989):336-9. doi: 10.1126/science.1188158.
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The lytic transcriptome of Kaposi's sarcoma-associated herpesvirus reveals extensive transcription of noncoding regions, including regions antisense to important genes.卡波氏肉瘤相关疱疹病毒的裂解转录组揭示了广泛的非编码区域转录,包括与重要基因反义的区域。
J Virol. 2010 Aug;84(16):7934-42. doi: 10.1128/JVI.00645-10. Epub 2010 Jun 9.
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Making sense of antisense: seemingly noncoding RNAs antisense to the master regulator of Kaposi's sarcoma-associated herpesvirus lytic replication do not regulate that transcript but serve as mRNAs encoding small peptides.明白反义 RNA:与卡波西肉瘤相关疱疹病毒裂解复制的主调控因子反义的看似非编码 RNA 并不调节该转录本,而是作为编码小肽的 mRNA 发挥作用。
J Virol. 2010 Jun;84(11):5465-75. doi: 10.1128/JVI.02705-09. Epub 2010 Mar 31.
7
Array-based transcript profiling and limiting-dilution reverse transcription-PCR analysis identify additional latent genes in Kaposi's sarcoma-associated herpesvirus.基于阵列的转录谱分析和有限稀释反转录 PCR 分析鉴定卡波西肉瘤相关疱疹病毒中的其他潜伏基因。
J Virol. 2010 Jun;84(11):5565-73. doi: 10.1128/JVI.02723-09. Epub 2010 Mar 10.
8
Post-transcriptional processing generates a diversity of 5'-modified long and short RNAs.转录后加工产生了多种5'端修饰的长链和短链RNA。
Nature. 2009 Feb 19;457(7232):1028-32. doi: 10.1038/nature07759. Epub 2009 Jan 25.
9
3' end processing of a long nuclear-retained noncoding RNA yields a tRNA-like cytoplasmic RNA.一种长链核滞留非编码RNA的3'端加工产生一种类似tRNA的细胞质RNA。
Cell. 2008 Nov 28;135(5):919-32. doi: 10.1016/j.cell.2008.10.012.
10
A mobile functional region of Kaposi's sarcoma-associated herpesvirus ORF50 protein independently regulates DNA binding and protein abundance.卡波西肉瘤相关疱疹病毒ORF50蛋白的一个移动功能区域独立调节DNA结合和蛋白质丰度。
J Virol. 2008 Oct;82(19):9700-16. doi: 10.1128/JVI.00862-08. Epub 2008 Jul 23.

一种病毒编码的小肽调节 RTA 的稳定性并促进卡波西肉瘤相关疱疹病毒的裂解复制。

A virally encoded small peptide regulates RTA stability and facilitates Kaposi's sarcoma-associated herpesvirus lytic replication.

机构信息

Department of Microbiology, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

J Virol. 2013 Mar;87(6):3461-70. doi: 10.1128/JVI.02746-12. Epub 2013 Jan 9.

DOI:10.1128/JVI.02746-12
PMID:23302891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3592115/
Abstract

In both mammalian and viral genomes, a large proportion of sequences are transcribed and annotated as noncoding RNAs. A polyadenylated RNA of 3.0 kb (T3.0) is transcribed from the opposite strand of the open reading frame 50 (ORF50) DNA template in the genome of Kaposi's sarcoma-associated herpesvirus (KSHV) and has been annotated previously as a noncoding RNA. ORF50 encodes the replication and transcription activator (RTA), which controls the switch of the virus between the latent and lytic phases of the life cycle. Here we show that T3.0 encodes a small peptide of 48 amino acids (designated viral small peptide 1 [vSP-1]). vSP-1 interacts with RTA at the protein abundance regulatory signal (PARS) motifs, and the association prevents RTA from being subjected to degradation through the ubiquitin-proteasome pathway. As a consequence, vSP-1 facilitates KSHV gene expression and lytic replication. This finding reveals a novel mechanism of gene regulation in the viral life cycle.

摘要

在哺乳动物和病毒基因组中,很大一部分序列被转录并注释为非编码 RNA。从卡波济肉瘤相关疱疹病毒 (KSHV) 基因组中开放阅读框 50 (ORF50) DNA 模板的反义链转录出一个 3.0 kb 的多聚腺苷酸化 RNA (T3.0),先前已将其注释为非编码 RNA。ORF50 编码复制和转录激活剂 (RTA),它控制病毒在生命周期潜伏和裂解阶段之间的转换。在这里,我们表明 T3.0 编码一个 48 个氨基酸的小肽 (命名为病毒小肽 1 [vSP-1])。vSP-1 在蛋白丰度调节信号 (PARS) 基序上与 RTA 相互作用,这种结合阻止 RTA 通过泛素-蛋白酶体途径降解。因此,vSP-1 促进了 KSHV 的基因表达和裂解复制。这一发现揭示了病毒生命周期中基因调控的一种新机制。