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爱泼斯坦-巴尔病毒(EBV)早期蛋白EB2是一种在EBV转录因子EB1和R的控制下表达的转录后激活因子。

The Epstein-Barr virus (EBV) early protein EB2 is a posttranscriptional activator expressed under the control of EBV transcription factors EB1 and R.

作者信息

Buisson M, Manet E, Trescol-Biemont M C, Gruffat H, Durand B, Sergeant A

机构信息

Ecole Normale Supérieure de Lyon-Centre National de la Recherche Scientifique UMR49, Ecole Normale Supérieure de Lyon, France.

出版信息

J Virol. 1989 Dec;63(12):5276-84. doi: 10.1128/JVI.63.12.5276-5284.1989.

DOI:10.1128/JVI.63.12.5276-5284.1989
PMID:2555554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC251193/
Abstract

From the cloning and characterization of cDNAs, we found that the Epstein-Barr virus (EBV) open reading frame (ORF) BMLF1-BSLF2 coding for the early protein EB2 is present in several mRNAs generated by alternative splicing and expressed in the leftward direction from two promoters PM and PM1. The PM promoter controls the expression of two abundant mRNA species of 1.9 and 2 kilobases (kb), whereas the PM1 promoter controls the expression of at least three mRNAs 3.6, 4.0, and 4.4 kb long. The PM promoter probably overlaps with the PS promoter which controls the transcription of a 3.6-kb mRNA expressed in the rightward direction and containing the ORF BSRF1. Although it increases the amount of chloramphenicol acetyltransferase enzyme expressed from the chimeric pMCAT gene, EB2 is not a promiscuous trans-activator of gene expression and does not positively regulate its own expression from promoter PM. The EB2 activation is not promoter dependent but could possibly act by stabilizing mRNAs and increasing their translation. The PM promoter is, however, activated by the two EBV transcription trans-acting factors, EB1 and R, encoded by the EBV ORFs BZLF1 and BRLF1, respectively. EB1 activates the PM promoter from a consensus AP-1 binding site, and R activates the PM promoter from an enhancer.

摘要

通过对cDNA的克隆和特性分析,我们发现编码早期蛋白EB2的爱泼斯坦-巴尔病毒(EBV)开放阅读框(ORF)BMLF1 - BSLF2存在于通过可变剪接产生的几种mRNA中,并从两个启动子PM和PM1向左表达。PM启动子控制1.9和2千碱基(kb)的两种丰富mRNA种类的表达,而PM1启动子控制至少三种长度分别为3.6、4.0和4.4 kb的mRNA的表达。PM启动子可能与PS启动子重叠,PS启动子控制以向右方向表达且包含ORF BSRF1的3.6 kb mRNA的转录。尽管EB2增加了从嵌合pMCAT基因表达的氯霉素乙酰转移酶的量,但它不是基因表达的杂乱反式激活因子,也不会从启动子PM正向调节其自身表达。EB2的激活不依赖于启动子,但可能通过稳定mRNA并增加其翻译起作用。然而,PM启动子被分别由EBV ORFs BZLF1和BRLF1编码的两种EBV转录反式作用因子EB1和R激活。EB1从共有AP - 1结合位点激活PM启动子,而R从增强子激活PM启动子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/d942866c5b5f/jvirol00079-0304-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/1573fc276541/jvirol00079-0299-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/ccfb23b35f5b/jvirol00079-0301-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/ac678672f816/jvirol00079-0302-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/60f661f36e50/jvirol00079-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/7840602f6914/jvirol00079-0303-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/d942866c5b5f/jvirol00079-0304-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/1573fc276541/jvirol00079-0299-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/ccfb23b35f5b/jvirol00079-0301-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/ac678672f816/jvirol00079-0302-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/60f661f36e50/jvirol00079-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/7840602f6914/jvirol00079-0303-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a4e/251193/d942866c5b5f/jvirol00079-0304-a.jpg

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A cDNA cloning vector that permits expression of cDNA inserts in mammalian cells.一种允许在哺乳动物细胞中表达互补DNA插入片段的互补DNA克隆载体。
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Non-contiguous segments of the polyoma genome required in cis for DNA replication.多瘤病毒基因组中DNA复制顺式作用所需的非连续片段。
抑制作用 爱泼斯坦-巴尔病毒 溶原性激活 通过 非典型抗精神病药物 氯氮平。
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The splicing factor SRSF3 is functionally connected to the nuclear RNA exosome for intronless mRNA decay.剪接因子 SRSF3 与核 RNA 外切体在功能上相连,用于无内含子 mRNA 的降解。
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Transfer of the UAP56 interaction motif of human cytomegalovirus pUL69 to its murine cytomegalovirus homolog converts the protein into a functional mRNA export factor that can substitute for pUL69 during viral infection.人巨细胞病毒 pUL69 的 UAP56 相互作用基序转移到其鼠巨细胞病毒同源物中,将该蛋白转化为功能性 mRNA 输出因子,可在病毒感染期间替代 pUL69。
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Characterization of the betaherpesviral pUL69 protein family reveals binding of the cellular mRNA export factor UAP56 as a prerequisite for stimulation of nuclear mRNA export and for efficient viral replication.β疱疹病毒 pUL69 蛋白家族的特征表明,与细胞 mRNA 输出因子 UAP56 的结合是刺激核 mRNA 输出和有效病毒复制的前提条件。
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Two small RNAs encoded by Epstein-Barr virus and complexed with protein are precipitated by antibodies from patients with systemic lupus erythematosus.由爱泼斯坦-巴尔病毒编码并与蛋白质复合的两种小RNA被系统性红斑狼疮患者的抗体沉淀下来。
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DNA sequence and expression of the B95-8 Epstein-Barr virus genome.B95-8型爱泼斯坦-巴尔病毒基因组的DNA序列与表达
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Both Epstein-Barr virus (EBV)-encoded trans-acting factors, EB1 and EB2, are required to activate transcription from an EBV early promoter.爱泼斯坦-巴尔病毒(EBV)编码的反式作用因子EB1和EB2都是激活EBV早期启动子转录所必需的。
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J Virol. 1986 Oct;60(1):140-8. doi: 10.1128/JVI.60.1.140-148.1986.