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Nat Commun. 2017 Apr 21;8:15087. doi: 10.1038/ncomms15087.
2
Promoter Motifs in NCLDVs: An Evolutionary Perspective.核质大DNA病毒中的启动子基序:进化视角
Viruses. 2017 Jan 20;9(1):16. doi: 10.3390/v9010016.
3
Morphological and Taxonomic Properties of Tokyovirus, the First Marseilleviridae Member Isolated from Japan.东京病毒的形态学和分类学特性,首个从日本分离出的马赛病毒科成员
Microbes Environ. 2016 Dec 23;31(4):442-448. doi: 10.1264/jsme2.ME16107. Epub 2016 Nov 19.
4
Marseillevirus in the Pharynx of a Patient with Neurologic Disorders.一名神经系统疾病患者咽部的马赛病毒
Emerg Infect Dis. 2016 Nov;22(11):2008-2010. doi: 10.3201/eid2211.160189.
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Marseillevirus in lymphoma: a giant in the lymph node.马塞利亚病毒与淋巴瘤:淋巴结中的巨无霸
Lancet Infect Dis. 2016 Oct;16(10):e225-e234. doi: 10.1016/S1473-3099(16)30051-2. Epub 2016 Aug 5.
6
A Brazilian Marseillevirus Is the Founding Member of a Lineage in Family Marseilleviridae.一种巴西马赛病毒是马赛病毒科一个谱系的创始成员。
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7
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8
Genome analysis of the first Marseilleviridae representative from Australia indicates that most of its genes contribute to virus fitness.对来自澳大利亚的首个马赛病毒科代表病毒进行的基因组分析表明,其大多数基因对病毒适应性有贡献。
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9
Complete genome sequence of Tunisvirus, a new member of the proposed family Marseilleviridae.突尼斯病毒全基因组序列,一种拟议的马赛病毒科新成员。
Arch Virol. 2014 Sep;159(9):2349-58. doi: 10.1007/s00705-014-2023-5. Epub 2014 Apr 26.
10
First isolation of a Marseillevirus in the Diptera Syrphidae Eristalis tenax.首次在双翅目食蚜蝇科 Eristalis tenax 中分离出马塞病毒。
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马赛病毒启动子序列的研究凸显了基因间区域中AAATATTT基序的显著丰富性。

The Investigation of Promoter Sequences of Marseilleviruses Highlights a Remarkable Abundance of the AAATATTT Motif in Intergenic Regions.

作者信息

Oliveira Graziele Pereira, Lima Maurício Teixeira, Arantes Thalita Souza, Assis Felipe Lopes, Rodrigues Rodrigo Araújo Lima, da Fonseca Flávio Guimarães, Bonjardim Cláudio Antônio, Kroon Erna Geessien, Colson Philippe, La Scola Bernard, Abrahão Jônatas Santos

机构信息

Laboratório de Vírus, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

URMITE, Aix Marseille Université, UM63, CNRS 7278, IRD 198, INSERM 1095, IHU-Méditerranée Infection, AP-HM, Marseille, France.

出版信息

J Virol. 2017 Oct 13;91(21). doi: 10.1128/JVI.01088-17. Print 2017 Nov 1.

DOI:10.1128/JVI.01088-17
PMID:28794030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5640848/
Abstract

Viruses display a wide range of genomic profiles and, consequently, a variety of gene expression strategies. Specific sequences associated with transcriptional processes have been described in viruses, and putative promoter motifs have been elucidated for some nucleocytoplasmic large DNA viruses (NCLDV). Among NCLDV, the is a well-recognized family because of its genomic mosaicism. The marseilleviruses have an ability to incorporate foreign genes, especially from sympatric organisms inhabiting , its main known host. Here, we identified for the first time an eight-nucleotide A/T-rich promoter sequence (AAATATTT) associated with 55% of marseillevirus genes that is conserved in all marseilleviruses lineages, a higher level of conservation than that of any giant virus described to date. We instigated our prediction about the promoter motif by biological assays and by evaluating how single mutations in this octamer can impact gene expression. The investigation of sequences that regulate the expression of genes relative to lateral transfer revealed that the promoter motifs do not appear to be incorporated by marseilleviruses from donor organisms. Indeed, analyses of the intergenic regions that regulate lateral gene transfer-related genes have revealed an independent origin of the marseillevirus intergenic regions that does not match gene-donor organisms. About 50% of AAATATTT motifs spread throughout intergenic regions of the marseilleviruses are present as multiple copies. We believe that such multiple motifs are associated with increased expression of a given gene or are related to incorporation of foreign genes into the mosaic genome of marseilleviruses. The marseilleviruses draw attention because of the peculiar features of their genomes; however, little is known about their gene expression patterns or the factors that regulate those expression patterns. The limited published research on the expression patterns of the marseilleviruses and their unique genomes has led us to study the promoter motif sequences in the intergenic regions of the marseilleviruses. This work is the first to analyze promoter sequences in the genomes of the marseilleviruses. We also suggest a strong capacity to acquire foreign genes and to express those genes mediated by multiple copies of the promoter motifs available in intergenic regions. These findings contribute to an understanding of genomic expansion and plasticity observed in these giant viruses.

摘要

病毒呈现出广泛的基因组图谱,因此也有各种各样的基因表达策略。病毒中已描述了与转录过程相关的特定序列,并且已阐明了一些核质大DNA病毒(NCLDV)的假定启动子基序。在NCLDV中,马赛病毒因其基因组镶嵌性而成为一个广为人知的家族。马赛病毒有能力整合外源基因,尤其是来自其主要已知宿主——栖息于同一区域的共生生物的基因。在这里,我们首次鉴定出一个富含A/T的八核苷酸启动子序列(AAATATTT),该序列与55%的马赛病毒基因相关,并且在所有马赛病毒谱系中都保守,其保守程度高于迄今为止描述的任何巨型病毒。我们通过生物学试验以及评估该八聚体中的单个突变如何影响基因表达来验证我们对启动子基序的预测。对相对于横向转移调节基因表达的序列的研究表明,启动子基序似乎不是由马赛病毒从供体生物中整合而来的。事实上,对调节横向基因转移相关基因的基因间区域的分析揭示了马赛病毒基因间区域的独立起源,这与基因供体生物不匹配。分布在马赛病毒基因间区域的AAATATTT基序中约50%以多个拷贝的形式存在。我们认为,这种多个基序与给定基因表达的增加相关,或者与外源基因整合到马赛病毒的镶嵌基因组中有关。马赛病毒因其基因组的独特特征而备受关注;然而,人们对它们的基因表达模式或调节这些表达模式的因素知之甚少。关于马赛病毒表达模式及其独特基因组的已发表研究有限,这促使我们研究马赛病毒基因间区域的启动子基序序列。这项工作是首次分析马赛病毒基因组中的启动子序列。我们还提出,马赛病毒具有强大的获取外源基因并由基因间区域中可用的启动子基序多个拷贝介导表达这些基因的能力。这些发现有助于理解在这些巨型病毒中观察到的基因组扩展和可塑性。