• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

A组赛内卡病毒多聚蛋白的翻译起始于IRES近端起始密码子。

Translation of Senecavirus A polyprotein is initiated from the IRES-proximal initiation codon.

作者信息

Wang Qianqian, Zhao Di, Wang Ling, Sang Yuxuan, Meng Hailan, Wang Qi, Shan Hu, Liu Fuxiao, Geri Letu

机构信息

College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot, 010011, China.

College of Veterinary Medicine, Qingdao Agricultural University, Qingdao, 266109, China.

出版信息

Virology. 2023 Feb;579:67-74. doi: 10.1016/j.virol.2022.12.009. Epub 2022 Dec 30.

DOI:10.1016/j.virol.2022.12.009
PMID:36608596
Abstract

To clarify whether Senecavirus A (SVA) has the potential of alternative translation, an extra G residue was inserted into an SVA cDNA clone, resultantly generating an "AUGAUG" motif. The second AUG is the authentic SVA initiation codon, whereas the first AUG is a putative one. Subsequently, eighteen nucleotides were inserted one by one between AUG and AUG for reconstructing cDNA clones. The test of virus recovery showed that three replication-competent SVAs, whose AUG/AUG-flanked sequences were not multiples of three nucleotides, were successfully rescued from their individual cDNA clones. The wild-type SVA possesses a UUUUU motif within the polyprotein-encoding region. Sanger sequencing showed that these three replication-competent SVAs harbored one or two extra U residues in the UUUUU motif, implying that polyprotein translation was initiated from the putative AUG, and the authentic AUG would be inactivated. This is probably attributed to the lack of ribosome scanning along an SVA genome.

摘要

为了阐明A组赛尼卡病毒(SVA)是否具有可变翻译的潜力,在一个SVA cDNA克隆中插入了一个额外的G残基,从而产生了一个“AUGAUG”基序。第二个AUG是SVA真正的起始密码子,而第一个AUG是一个推定的起始密码子。随后,在AUG和AUG之间逐个插入18个核苷酸以重建cDNA克隆。病毒拯救试验表明,从其各自的cDNA克隆中成功拯救出了三种具有复制能力的SVA,其AUG/AUG侧翼序列不是三个核苷酸的倍数。野生型SVA在多聚蛋白编码区内具有一个UUUUU基序。桑格测序表明,这三种具有复制能力的SVA在UUUUU基序中含有一个或两个额外的U残基,这意味着多聚蛋白翻译是从推定的AUG起始的,而真正的AUG将失活。这可能归因于缺乏沿SVA基因组的核糖体扫描。

相似文献

1
Translation of Senecavirus A polyprotein is initiated from the IRES-proximal initiation codon.A组赛内卡病毒多聚蛋白的翻译起始于IRES近端起始密码子。
Virology. 2023 Feb;579:67-74. doi: 10.1016/j.virol.2022.12.009. Epub 2022 Dec 30.
2
Experimental evidence for occurrence of putative copy-choice recombination between two Senecavirus A genomes.实验证据表明,两种塞尼卡病毒 A 基因组之间存在假定的拷贝选择重组。
Vet Microbiol. 2022 Aug;271:109487. doi: 10.1016/j.vetmic.2022.109487. Epub 2022 Jun 6.
3
Motif mutations in pseudoknot stem I upstream of start codon in Senecavirus A genome: Impacts on activity of viral IRES and on rescue of recombinant virus.塞尼卡病毒 A 基因组起始密码子上游假结茎 I 中的模体突变:对病毒 IRES 活性和重组病毒拯救的影响。
Vet Microbiol. 2021 Nov;262:109223. doi: 10.1016/j.vetmic.2021.109223. Epub 2021 Sep 2.
4
The influence of downstream protein-coding sequence on internal ribosome entry on hepatitis C virus and other flavivirus RNAs.下游蛋白质编码序列对丙型肝炎病毒及其他黄病毒RNA内部核糖体进入的影响。
RNA. 2001 Apr;7(4):585-97. doi: 10.1017/s1355838201000589.
5
Translation of the F protein of hepatitis C virus is initiated at a non-AUG codon in a +1 reading frame relative to the polyprotein.丙型肝炎病毒F蛋白的翻译起始于相对于多聚蛋白的+1读码框中的一个非AUG密码子。
Nucleic Acids Res. 2005 Mar 8;33(5):1474-86. doi: 10.1093/nar/gki292. Print 2005.
6
Identification of cis-acting replication element in VP2-encoding region of Senecavirus A genome.鉴定塞尼卡病毒 A 基因组 VP2 编码区的顺式作用复制元件。
Vet Microbiol. 2023 May;280:109717. doi: 10.1016/j.vetmic.2023.109717. Epub 2023 Mar 2.
7
Stem II-disrupting pseudoknot does not abolish ability of Senecavirus A IRES to initiate protein expression, but inhibits recovery of virus from cDNA clone.茎 II 干扰假结并不消除塞内卡病毒 IRES 起始蛋白表达的能力,但抑制了病毒从 cDNA 克隆中的恢复。
Vet Microbiol. 2021 Apr;255:109024. doi: 10.1016/j.vetmic.2021.109024. Epub 2021 Mar 2.
8
Only fourteen 3'-end poly(A)s sufficient for rescuing Senecavirus A from its cDNA clone, but inadequate to meet requirement of viral replication.仅 14 个 3' 端 poly(A) 足以拯救从其 cDNA 克隆中分离的塞内卡病毒 A,但不足以满足病毒复制的要求。
Virus Res. 2023 Apr 15;328:199076. doi: 10.1016/j.virusres.2023.199076. Epub 2023 Mar 1.
9
The 5'-end motif of Senecavirus A cDNA clone is genetically modified in 36 different ways for uncovering profiles of virus recovery.为了揭示病毒恢复情况,对A组赛尼卡病毒cDNA克隆的5'端基序进行了36种不同方式的基因改造。
Front Microbiol. 2022 Aug 17;13:957849. doi: 10.3389/fmicb.2022.957849. eCollection 2022.
10
Impacts of single nucleotide deletions from the 3' end of Senecavirus A 5' untranslated region on activity of viral IRES and on rescue of recombinant virus.Senecavirus A 5'UTR 3'末端单核苷酸缺失对病毒 IRES 活性和重组病毒拯救的影响。
Virology. 2021 Nov;563:126-133. doi: 10.1016/j.virol.2021.09.002. Epub 2021 Sep 9.