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生物信息学分析表明,环状病毒VP6顺反子编码一个重叠基因。

Bioinformatic analysis suggests that the Orbivirus VP6 cistron encodes an overlapping gene.

作者信息

Firth Andrew E

机构信息

Department of Biochemistry, BioSciences Institute, University College Cork, Cork, Ireland.

出版信息

Virol J. 2008 Apr 14;5:48. doi: 10.1186/1743-422X-5-48.

Abstract

BACKGROUND

The genus Orbivirus includes several species that infect livestock - including Bluetongue virus (BTV) and African horse sickness virus (AHSV). These viruses have linear dsRNA genomes divided into ten segments, all of which have previously been assumed to be monocistronic.

RESULTS

Bioinformatic evidence is presented for a short overlapping coding sequence (CDS) in the Orbivirus genome segment 9, overlapping the VP6 cistron in the +1 reading frame. In BTV, a 77-79 codon AUG-initiated open reading frame (hereafter ORFX) is present in all 48 segment 9 sequences analysed. The pattern of base variations across the 48-sequence alignment indicates that ORFX is subject to functional constraints at the amino acid level (even when the constraints due to coding in the overlapping VP6 reading frame are taken into account; MLOGD software). In fact the translated ORFX shows greater amino acid conservation than the overlapping region of VP6. The ORFX AUG codon has a strong Kozak context in all 48 sequences. Each has only one or two upstream AUG codons, always in the VP6 reading frame, and (with a single exception) always with weak or medium Kozak context. Thus, in BTV, ORFX may be translated via leaky scanning. A long (83-169 codon) ORF is present in a corresponding location and reading frame in all other Orbivirus species analysed except Saint Croix River virus (SCRV; the most divergent). Again, the pattern of base variations across sequence alignments indicates multiple coding in the VP6 and ORFX reading frames.

CONCLUSION

At approximately 9.5 kDa, the putative ORFX product in BTV is too small to appear on most published protein gels. Nonetheless, a review of past literature reveals a number of possible detections. We hope that presentation of this bioinformatic analysis will stimulate an attempt to experimentally verify the expression and functional role of ORFX, and hence lead to a greater understanding of the molecular biology of these important pathogens.

摘要

背景

环状病毒属包含几种感染家畜的病毒——包括蓝舌病病毒(BTV)和非洲马瘟病毒(AHSV)。这些病毒具有线性双链RNA基因组,分为十个片段,此前一直认为所有片段都是单顺反子的。

结果

提供了生物信息学证据,表明环状病毒基因组片段9中存在一个短的重叠编码序列(CDS),在+1阅读框中与VP6顺反子重叠。在BTV中,在分析的所有48个片段9序列中都存在一个77 - 79密码子的AUG起始开放阅读框(以下简称ORFX)。48个序列比对中的碱基变异模式表明,ORFX在氨基酸水平上受到功能限制(即使考虑到在重叠的VP阅读框中编码所导致的限制;MLOGD软件)。实际上,翻译后的ORFX显示出比VP6重叠区域更高的氨基酸保守性。ORFX的AUG密码子在所有48个序列中都具有很强的科扎克序列背景。每个序列只有一两个上游AUG密码子,总是在VP6阅读框中,并且(有一个例外)总是具有弱或中等的科扎克序列背景。因此,在BTV中,ORFX可能通过漏扫描进行翻译。在除圣克罗伊河病毒(SCRV;差异最大的病毒)之外的所有其他分析的环状病毒物种的相应位置和阅读框中都存在一个长的(83 - 169密码子)开放阅读框。同样,序列比对中的碱基变异模式表明在VP6和ORFX阅读框中存在多重编码。

结论

在BTV中,假定的ORFX产物约为9.5 kDa,太小而无法在大多数已发表的蛋白质凝胶上出现。尽管如此,对过去文献的回顾揭示了一些可能的检测结果。我们希望展示这种生物信息学分析将促使人们尝试通过实验验证ORFX的表达和功能作用,并因此增进对这些重要病原体分子生物学的理解。

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