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1
Characterization of ribonucleoprotein complexes containing an abundant polyadenylated nuclear RNA encoded by Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8).对含有由卡波西肉瘤相关疱疹病毒(人类疱疹病毒8型)编码的丰富多聚腺苷酸化核RNA的核糖核蛋白复合物的表征。
J Virol. 1997 Feb;71(2):1207-12. doi: 10.1128/JVI.71.2.1207-1212.1997.
2
Discovery of Kaposi's sarcoma herpesvirus-encoded circular RNAs and a human antiviral circular RNA.卡波氏肉瘤相关疱疹病毒编码的环状 RNA 的发现和一种人类抗病毒环状 RNA。
Proc Natl Acad Sci U S A. 2018 Dec 11;115(50):12805-12810. doi: 10.1073/pnas.1816183115. Epub 2018 Nov 19.
3
Transcription activation of polyadenylated nuclear rna by rta in human herpesvirus 8/Kaposi's sarcoma-associated herpesvirus.人疱疹病毒8/卡波西肉瘤相关疱疹病毒中RTA对多聚腺苷酸化核RNA的转录激活作用
J Virol. 2001 Apr;75(7):3129-40. doi: 10.1128/JVI.75.7.3129-3140.2001.
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Patterns of gene expression and a transactivation function exhibited by the vGCR (ORF74) chemokine receptor protein of Kaposi's sarcoma-associated herpesvirus.卡波西肉瘤相关疱疹病毒的vGCR(ORF74)趋化因子受体蛋白所呈现的基因表达模式及反式激活功能。
J Virol. 2002 Apr;76(7):3421-39. doi: 10.1128/jvi.76.7.3421-3439.2002.
5
Transcriptome analysis of Kaposi's sarcoma-associated herpesvirus during de novo primary infection of human B and endothelial cells.人类B细胞和内皮细胞初次原发性感染期间卡波西肉瘤相关疱疹病毒的转录组分析
J Virol. 2015 Mar;89(6):3093-111. doi: 10.1128/JVI.02507-14. Epub 2014 Dec 31.
6
Kaposi's Sarcoma-Associated Herpesvirus Hijacks RNA Polymerase II To Create a Viral Transcriptional Factory.卡波西肉瘤相关疱疹病毒劫持RNA聚合酶II以创建病毒转录工厂。
J Virol. 2017 May 12;91(11). doi: 10.1128/JVI.02491-16. Print 2017 Jun 1.
7
CCAAT/enhancer-binding protein-alpha is induced during the early stages of Kaposi's sarcoma-associated herpesvirus (KSHV) lytic cycle reactivation and together with the KSHV replication and transcription activator (RTA) cooperatively stimulates the viral RTA, MTA, and PAN promoters.CCAAT/增强子结合蛋白α在卡波西肉瘤相关疱疹病毒(KSHV)裂解周期重新激活的早期阶段被诱导,并与KSHV复制和转录激活因子(RTA)协同刺激病毒的RTA、MTA和PAN启动子。
J Virol. 2003 Sep;77(17):9590-612. doi: 10.1128/jvi.77.17.9590-9612.2003.
8
Identification, expression, and immunogenicity of Kaposi's sarcoma-associated herpesvirus-encoded small viral capsid antigen.卡波西肉瘤相关疱疹病毒编码的小病毒衣壳抗原的鉴定、表达及免疫原性
J Virol. 1997 Apr;71(4):3069-76. doi: 10.1128/JVI.71.4.3069-3076.1997.
9
Kaposi's Sarcoma-Associated Herpesvirus mRNA Accumulation in Nuclear Foci Is Influenced by Viral DNA Replication and Viral Noncoding Polyadenylated Nuclear RNA.卡波西肉瘤相关疱疹病毒 mRNA 在核斑点中的积累受病毒 DNA 复制和病毒非编码多聚腺苷酸化核 RNA 的影响。
J Virol. 2018 Jun 13;92(13). doi: 10.1128/JVI.00220-18. Print 2018 Jul 1.
10
Transcription profile of Kaposi's sarcoma-associated herpesvirus in primary Kaposi's sarcoma lesions as determined by real-time PCR arrays.通过实时PCR阵列测定的原发性卡波西肉瘤病变中卡波西肉瘤相关疱疹病毒的转录谱。
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Dynamic bulge nucleotides in the KSHV PAN ENE triple helix provide a unique binding platform for small molecule ligands.在 KSHV PAN ENE 三螺旋中动态膨胀的核苷酸为小分子配体提供了独特的结合平台。
Nucleic Acids Res. 2021 Dec 16;49(22):13179-13193. doi: 10.1093/nar/gkab1170.
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Minichromosome Maintenance Proteins Cooperate with LANA during the G/S Phase of the Cell Cycle To Support Viral DNA Replication.微小染色体维持蛋白在细胞周期的 G/S 期与 LANA 合作,以支持病毒 DNA 复制。
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Gammaherpesvirus Readthrough Transcription Generates a Long Non-Coding RNA That Is Regulated by Antisense miRNAs and Correlates with Enhanced Lytic Replication In Vivo.γ疱疹病毒通读转录产生一种长链非编码RNA,该RNA受反义miRNA调控,并与体内增强的裂解复制相关。
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Two herpesviral noncoding PAN RNAs are functionally homologous but do not associate with common chromatin loci.两种疱疹病毒非编码 PAN RNAs 在功能上是同源的,但不与常见的染色质位点相关联。
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9
Expression of the Antisense-to-Latency Transcript Long Noncoding RNA in Kaposi's Sarcoma-Associated Herpesvirus.卡波西肉瘤相关疱疹病毒中潜伏期转录反义长链非编码RNA的表达
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10
Interactions between Giardia duodenalis Sm proteins and their association with spliceosomal snRNAs.十二指肠贾第虫Sm蛋白之间的相互作用及其与剪接体小核RNA的关联。
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本文引用的文献

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Kaposi's sarcoma-associated herpesvirus gene expression in endothelial (spindle) tumor cells.卡波西肉瘤相关疱疹病毒基因在内皮(梭形)肿瘤细胞中的表达。
J Virol. 1997 Jan;71(1):715-9. doi: 10.1128/JVI.71.1.715-719.1997.
2
KSHV antibodies among Americans, Italians and Ugandans with and without Kaposi's sarcoma.患有和未患卡波西肉瘤的美国人、意大利人和乌干达人中的卡波西肉瘤相关疱疹病毒抗体
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The seroepidemiology of human herpesvirus 8 (Kaposi's sarcoma-associated herpesvirus): distribution of infection in KS risk groups and evidence for sexual transmission.人类疱疹病毒8型(卡波西肉瘤相关疱疹病毒)的血清流行病学:在卡波西肉瘤风险人群中的感染分布及性传播证据
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4
Restricted expression of Kaposi sarcoma-associated herpesvirus (human herpesvirus 8) genes in Kaposi sarcoma.卡波西肉瘤相关疱疹病毒(人类疱疹病毒8型)基因在卡波西肉瘤中的限制性表达
Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6641-6. doi: 10.1073/pnas.93.13.6641.
5
A novel spliceosome containing U11, U12, and U5 snRNPs excises a minor class (AT-AC) intron in vitro.一种包含U11、U12和U5小核核糖核蛋白颗粒(snRNP)的新型剪接体在体外切除一个小类(AT-AC)内含子。
Cell. 1996 Mar 8;84(5):801-11. doi: 10.1016/s0092-8674(00)81057-0.
6
Lytic growth of Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8) in culture.卡波西肉瘤相关疱疹病毒(人类疱疹病毒8型)在培养中的裂解性生长。
Nat Med. 1996 Mar;2(3):342-6. doi: 10.1038/nm0396-342.
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Requirement of U12 snRNA for in vivo splicing of a minor class of eukaryotic nuclear pre-mRNA introns.U12 snRNA对一类次要的真核细胞核前体mRNA内含子体内剪接的需求
Science. 1996 Mar 22;271(5256):1716-8. doi: 10.1126/science.271.5256.1716.
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Frequent presence of a novel herpesvirus genome in lesions of human immunodeficiency virus-negative Kaposi's sarcoma.新型疱疹病毒基因组频繁出现在人类免疫缺陷病毒阴性的卡波西肉瘤病变中。
J Infect Dis. 1996 Jan;173(1):248-51. doi: 10.1093/infdis/173.1.248.
9
Mutation of an RSV intronic element abolishes both U11/U12 snRNP binding and negative regulation of splicing.呼吸道合胞病毒内含子元件的突变会消除U11/U12核小核糖核蛋白的结合以及剪接的负调控。
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10
m3G cap hypermethylation of U1 small nuclear ribonucleoprotein (snRNP) in vitro: evidence that the U1 small nuclear RNA-(guanosine-N2)-methyltransferase is a non-snRNP cytoplasmic protein that requires a binding site on the Sm core domain.体外U1小核核糖核蛋白(snRNP)的m3G帽超甲基化:U1小核RNA -(鸟苷-N2)-甲基转移酶是一种非snRNP细胞质蛋白,需要Sm核心结构域上的结合位点的证据。
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对含有由卡波西肉瘤相关疱疹病毒(人类疱疹病毒8型)编码的丰富多聚腺苷酸化核RNA的核糖核蛋白复合物的表征。

Characterization of ribonucleoprotein complexes containing an abundant polyadenylated nuclear RNA encoded by Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8).

作者信息

Zhong W, Ganem D

机构信息

Howard Hughes Medical Institute and Department of Microbiology, University of California-San Francisco, 94143-0414, USA.

出版信息

J Virol. 1997 Feb;71(2):1207-12. doi: 10.1128/JVI.71.2.1207-1212.1997.

DOI:10.1128/JVI.71.2.1207-1212.1997
PMID:8995643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC191174/
Abstract

Infection with Kaposi's sarcoma-associated herpesvirus (KSHV) (also called human herpesvirus 8) is strongly linked to all forms of Kaposi's sarcoma. We have previously identified two polyadenylated KSHV transcripts that are actively transcribed in Kaposi's sarcoma (KS) tumors and in KSHV-infected B-lymphoma cells. One of these RNAs (termed T1.1 or nut-1 RNA) is a 1.1-kb transcript present in a subpopulation of KS tumor cells. This RNA is localized to the nucleus of infected cells and has no open reading frames longer than 62 codons, suggesting that it may not function as an mRNA in vivo. Here we demonstrate that nut-1 RNA is a lytic-cycle gene product that is found in high-molecular-weight ribonucleoprotein complexes in infected cell nuclei. The transcript lacks the trimethylguanosine (TMG) cap found in many U-like small nuclear RNAs, but a subpopulation of nut-1 RNAs can associate with Sm protein-containing small nuclear ribonucleoproteins, as judged by immunoprecipitation analyses using monoclonal anti-Sm and anti-TMG antibodies. This interaction does not require other viral gene products, and deletion of the sole candidate Sm binding site on nut-1 RNA does not ablate this association. This finding suggests an indirect interaction with Sm-containing structures, and models for such associations are presented.

摘要

卡波西肉瘤相关疱疹病毒(KSHV)(也称为人类疱疹病毒8型)感染与所有形式的卡波西肉瘤密切相关。我们之前已经鉴定出两种多聚腺苷酸化的KSHV转录本,它们在卡波西肉瘤(KS)肿瘤和KSHV感染的B淋巴瘤细胞中活跃转录。其中一种RNA(称为T1.1或nut-1 RNA)是一种1.1 kb的转录本,存在于KS肿瘤细胞的一个亚群中。这种RNA定位于受感染细胞的细胞核,并且没有长度超过62个密码子的开放阅读框,这表明它在体内可能不作为mRNA发挥作用。在这里,我们证明nut-1 RNA是一种裂解周期基因产物,存在于受感染细胞核中的高分子量核糖核蛋白复合物中。该转录本缺乏许多U样小核RNA中发现的三甲基鸟苷(TMG)帽,但通过使用单克隆抗Sm和抗TMG抗体的免疫沉淀分析判断,nut-1 RNA的一个亚群可以与含Sm蛋白的小核核糖核蛋白结合。这种相互作用不需要其他病毒基因产物,并且删除nut-1 RNA上唯一的候选Sm结合位点并不会消除这种结合。这一发现表明与含Sm结构存在间接相互作用,并提出了这种结合的模型。