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桃褪绿斑驳病毒全基因组分析:非AUG起始密码子的鉴定、体外外壳蛋白表达及血清学交叉反应的阐明

Analysis of the complete genome of peach chlorotic mottle virus: identification of non-AUG start codons, in vitro coat protein expression, and elucidation of serological cross-reactions.

作者信息

James D, Varga A, Croft H

机构信息

Centre for Plant Health, Research Section, Sidney Laboratory, Canadian Food Inspection Agency, Sidney, British Columbia, Canada.

出版信息

Arch Virol. 2007;152(12):2207-15. doi: 10.1007/s00705-007-1050-x. Epub 2007 Sep 22.

Abstract

The entire genome of peach chlorotic mottle virus (PCMV), originally identified as Prunus persica cv. Agua virus (4N6), was sequenced and analysed. PCMV cross-reacts with antisera to diverse viruses, such as plum pox virus (PPV), genus Potyvirus, family Potyviridae; and apple stem pitting virus (ASPV), genus Foveavirus, family Flexiviridae. The PCMV genome consists of 9005 nucleotides (nts), excluding a poly(A) tail at the 3' end of the genome. Five open reading frames (ORFs) were identified with four untranslated regions (UTR) including a 5', a 3', and two intergenic UTRs. The genome organisation of PCMV is similar to that of ASPV and the two genomes share a nucleotide (nt) sequence identity of 58%. PCMV ORF1 encodes the replication-associated protein complex (Mr 241,503), ORF2-ORF4 code for the triple gene block proteins (TGBp; Mr 24,802, 12,370, and 7320, respectively), and ORF5 encodes the coat protein (CP) (Mr 42,505). Two non-AUG start codons participate in the initiation of translation: 35AUC and 7676AUA initiate translation of ORF1 and ORF5. In vitro expression with subsequent Western blot analysis confirmed ORF5 as the CP-encoding gene and confirmed that the codon AUA is able to initiate translation of the CP. Expression of a truncated CP fragment (Mr 39, 689) was demonstrated, and both proteins are expressed in vivo, since both were observed in Western blot analysis of PCMV-infected peach and Nicotiana occidentalis. The expressed proteins cross-reacted with an antiserum against ASPV. The amino acid sequences of the CPs of PCMV and ASPV CP share only 37% identity, but there are 11 shared peptides 4-8 aa residues long. These may constitute linear epitopes responsible for ASPV antiserum cross reactions. No significant common linear epitopes were associated with PPV. Extensive phylogenetic analysis indicates that PCMV is closely related to ASPV and is a new and distinct member of the genus Foveavirus.

摘要

对最初鉴定为李属阿瓜病毒(4N6)的桃褪绿斑驳病毒(PCMV)的全基因组进行了测序和分析。PCMV与多种病毒的抗血清发生交叉反应,如马铃薯Y病毒属的李痘病毒(PPV)、马铃薯Y病毒科;以及凹脉病毒属的苹果茎痘病毒(ASPV)、柔线病毒科。PCMV基因组由9005个核苷酸(nt)组成,不包括基因组3'端的聚腺苷酸(A)尾。鉴定出五个开放阅读框(ORF)和四个非翻译区(UTR),包括一个5'UTR、一个3'UTR和两个基因间隔区UTR。PCMV的基因组结构与ASPV相似,两个基因组的核苷酸(nt)序列同一性为58%。PCMV的ORF1编码复制相关蛋白复合体(分子量241,503),ORF2 - ORF4编码三基因块蛋白(TGBp;分子量分别为24,802、12,370和7320),ORF5编码外壳蛋白(CP)(分子量42,505)。两个非AUG起始密码子参与翻译起始:35AUC和7676AUA分别起始ORF1和ORF5的翻译。体外表达及随后的蛋白质印迹分析证实ORF5为编码CP的基因,并证实密码子AUA能够起始CP的翻译。证明了截短的CP片段(分子量39,689)的表达,且两种蛋白均在体内表达,因为在感染PCMV的桃和西方烟草的蛋白质印迹分析中均观察到了这两种蛋白。表达的蛋白与抗ASPV抗血清发生交叉反应。PCMV的CP和ASPV的CP的氨基酸序列仅具有37%的同一性,但有11个长度为4 - 8个氨基酸残基的共享肽段。这些可能构成了负责ASPV抗血清交叉反应的线性表位。与PPV没有显著的共同线性表位。广泛的系统发育分析表明,PCMV与ASPV密切相关,是凹脉病毒属的一个新的独特成员。

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