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首页> 外文期刊>Archives of virology >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.
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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.

机译:桃褪绿斑驳病毒完整基因组的分析:非AUG起始密码子的鉴定,体外外壳蛋白的表达以及血清学交叉反应的阐明。

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摘要

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 (M(r) 241,503), ORF2 - ORF4 code for the triple gene block proteins (TGBp; M(r) 24,802, 12,370, and 7320, respectively), and ORF5 encodes the coat protein (CP) (M(r) 42,505). Two non-AUG start codons participate in the initiation of translation: (35)AUC and (7676)AUA 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 (M(r) 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.
机译:桃绿叶斑驳病毒(PCMV)的整个基因组,最初被鉴定为李属李子(Prunus persica cv)。对阿瓜病毒(4N6)进行了测序和分析。 PCMV与抗血清能与多种病毒发生交叉反应,例如李子痘病毒(PPV),波多病毒属,波多病毒科;苹果花叶病毒(ASPV),凹叶病毒属,Flexiviridae家族。 PCMV基因组由9005个核苷酸(nts)组成,不包括基因组3'端的poly(A)尾巴。鉴定了五个开放阅读框(ORF)和四个非翻译区(UTR),包括5',3'和两个基因间UTR。 PCMV的基因组组织与ASPV相似,两个基因组的核苷酸(nt)序列同一性为58%。 PCMV ORF1编码与复制相关的蛋白质复合物(M(r)241,503),ORF2- ORF4编码三重基因阻断蛋白(TGBp; M(r)24,802、12,370和7320,分别),ORF5编码外壳蛋白(CP)(M(r)42,505)。两个非AUG起始密码子参与翻译的起始:(35)AUC和(7676)AUA起始ORF1和ORF5的翻译。体外表达和随后的蛋白质印迹分析证实了ORF5为CP编码基因,并确认密码子AUA能够启动CP的翻译。证实了截短的CP片段的表达(M(r)39,689),并且两种蛋白都在体内表达,因为在蛋白质印迹分析中均观察到了这两种蛋白,这些蛋白在PCMV感染的桃和西方烟草中均已观察到。表达的蛋白质与抗ASPV的抗血清交叉反应。 PCMV和ASPV CP的CP的氨基酸序列仅具有37%的同一性,但共有11个共有的肽,长度为4-8个氨基酸。这些可能构成负责ASPV抗血清交叉反应的线性表位。没有明显的常见线性表位与PPV相关。广泛的系统发育分析表明,PCMV与ASPV密切相关,并且是黄斑病毒属的新成员。

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