Picornavirus Evolution: Genomes Encoding Multiple 2ANPGP Sequences-Biomedical and Biotechnological Utility.

IF 3.8 3区 医学 Q2 VIROLOGY
Viruses-Basel Pub Date : 2024-10-09 DOI:10.3390/v16101587
Garry A Luke, Lauren S Ross, Yi-Ting Lo, Hsing-Chieh Wu, Martin D Ryan
{"title":"Picornavirus Evolution: Genomes Encoding Multiple 2A<sup>NPGP</sup> Sequences-Biomedical and Biotechnological Utility.","authors":"Garry A Luke, Lauren S Ross, Yi-Ting Lo, Hsing-Chieh Wu, Martin D Ryan","doi":"10.3390/v16101587","DOIUrl":null,"url":null,"abstract":"<p><p>Alignment of picornavirus proteinase/polymerase sequences reveals this family evolved into five 'supergroups'. Interestingly, the nature of the 2A region of the picornavirus polyprotein is highly correlated with this phylogeny. Viruses within supergroup 4, the <i>Paavivirinae</i>, have complex 2A regions with many viruses encoding multiple 2A<sup>NPGP</sup> sequences. In vitro transcription/translation analyses of a synthetic polyprotein comprising green fluorescent protein (GFP) linked to β-glucuronidase (GUS) via individual 2A<sup>NPGP</sup>s showed two main phenotypes: highly active 2A<sup>NPGP</sup> sequences-similar to foot-and-mouth disease virus 2A<sup>NPGP</sup>-and, surprisingly, a novel phenotype of some 2A<sup>NPGP</sup> sequences which apparently terminate translation at the C-terminus of 2A<sup>NPGP</sup> without detectable re-initiation of downstream sequences (GUS). Probing databases with the short sequences between 2A<sup>NPGP</sup>s did not reveal any potential 'accessory' functions. The novel, highly active, 2A-like sequences we identified substantially expand the toolbox for biomedical/biotechnological co-expression applications.</p>","PeriodicalId":49328,"journal":{"name":"Viruses-Basel","volume":"16 10","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512398/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Viruses-Basel","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/v16101587","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VIROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Alignment of picornavirus proteinase/polymerase sequences reveals this family evolved into five 'supergroups'. Interestingly, the nature of the 2A region of the picornavirus polyprotein is highly correlated with this phylogeny. Viruses within supergroup 4, the Paavivirinae, have complex 2A regions with many viruses encoding multiple 2ANPGP sequences. In vitro transcription/translation analyses of a synthetic polyprotein comprising green fluorescent protein (GFP) linked to β-glucuronidase (GUS) via individual 2ANPGPs showed two main phenotypes: highly active 2ANPGP sequences-similar to foot-and-mouth disease virus 2ANPGP-and, surprisingly, a novel phenotype of some 2ANPGP sequences which apparently terminate translation at the C-terminus of 2ANPGP without detectable re-initiation of downstream sequences (GUS). Probing databases with the short sequences between 2ANPGPs did not reveal any potential 'accessory' functions. The novel, highly active, 2A-like sequences we identified substantially expand the toolbox for biomedical/biotechnological co-expression applications.

皮卡病毒进化:编码多个 2ANPGP 序列的基因组--生物医学和生物技术用途。
皮卡病毒蛋白酶/聚合酶序列的比对显示,该家族进化为五个 "超群"。有趣的是,皮卡病毒多聚蛋白 2A 区的性质与这一系统发育高度相关。超群 4(Paavivirinae)中的病毒具有复杂的 2A 区域,许多病毒编码多个 2ANPGP 序列。对由绿色荧光蛋白(GFP)通过单个 2ANPGPs 与 β-葡萄糖醛酸酶(GUS)连接而成的合成多聚蛋白进行的体外转录/翻译分析显示出两种主要表型:高度活跃的 2ANPGP 序列--类似于口蹄疫病毒的 2ANPGP --以及令人惊讶的一些 2ANPGP 序列的新表型,它们显然在 2ANPGP 的 C 端终止翻译,而下游序列(GUS)却无法检测到重新启动。利用 2ANPGPs 之间的短序列探测数据库,没有发现任何潜在的 "附属 "功能。我们发现的新型、高活性、类似 2A 的序列大大扩展了生物医学/生物技术共表达应用的工具箱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Viruses-Basel
Viruses-Basel VIROLOGY-
CiteScore
7.30
自引率
12.80%
发文量
2445
审稿时长
1 months
期刊介绍: Viruses (ISSN 1999-4915) is an open access journal which provides an advanced forum for studies of viruses. It publishes reviews, regular research papers, communications, conference reports and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. We also encourage the publication of timely reviews and commentaries on topics of interest to the virology community and feature highlights from the virology literature in the ''News and Views'' section. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信