Suppr超能文献

西尼罗河病毒和日本脑炎黄病毒编码 NS2A 的序列中一个保守的预测假结表明 NS1' 可能源自核糖体移码。

A conserved predicted pseudoknot in the NS2A-encoding sequence of West Nile and Japanese encephalitis flaviviruses suggests NS1' may derive from ribosomal frameshifting.

作者信息

Firth Andrew E, Atkins John F

机构信息

BioSciences Institute, University College Cork, Cork, Ireland.

出版信息

Virol J. 2009 Feb 5;6:14. doi: 10.1186/1743-422X-6-14.

Abstract

Japanese encephalitis, West Nile, Usutu and Murray Valley encephalitis viruses form a tight subgroup within the larger Flavivirus genus. These viruses utilize a single-polyprotein expression strategy, resulting in ~10 mature proteins. Plotting the conservation at synonymous sites along the polyprotein coding sequence reveals strong conservation peaks at the very 5' end of the coding sequence, and also at the 5' end of the sequence encoding the NS2A protein. Such peaks are generally indicative of functionally important non-coding sequence elements. The second peak corresponds to a predicted stable pseudoknot structure whose biological importance is supported by compensatory mutations that preserve the structure. The pseudoknot is preceded by a conserved slippery heptanucleotide (Y CCU UUU), thus forming a classical stimulatory motif for -1 ribosomal frameshifting. We hypothesize, therefore, that the functional importance of the pseudoknot is to stimulate a portion of ribosomes to shift -1 nt into a short (45 codon), conserved, overlapping open reading frame, termed foo. Since cleavage at the NS1-NS2A boundary is known to require synthesis of NS2A in cis, the resulting transframe fusion protein is predicted to be NS1-NS2A(N-term)-FOO. We hypothesize that this may explain the origin of the previously identified NS1 'extension' protein in JEV-group flaviviruses, known as NS1'.

摘要

日本脑炎病毒、西尼罗河病毒、乌苏图病毒和墨累谷脑炎病毒在黄病毒属这个更大的分类中形成了一个紧密的亚群。这些病毒采用单多聚蛋白表达策略,产生约10种成熟蛋白。沿着多聚蛋白编码序列绘制同义位点的保守性图谱,发现在编码序列的5'端以及编码NS2A蛋白序列的5'端有强烈的保守峰。这样的峰通常指示功能重要的非编码序列元件。第二个峰对应于一个预测的稳定假结结构,其生物学重要性得到了维持该结构的补偿性突变的支持。假结之前是一个保守的七核苷酸滑序列(Y CCU UUU),从而形成了一个经典的-1核糖体移码刺激基序。因此,我们推测,假结的功能重要性在于刺激一部分核糖体将-1个核苷酸移码到一个短的(45个密码子)、保守的、重叠的开放阅读框,称为foo。由于已知在NS1-NS2A边界处的切割需要顺式合成NS2A,因此预测产生的移码融合蛋白为NS1-NS2A(N端)-FOO。我们推测,这可能解释了在JEV组黄病毒中先前鉴定的NS1“延伸”蛋白(称为NS1')的起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b6b/2657137/0174ac293c83/1743-422X-6-14-1.jpg

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