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星状病毒假定基因组连接病毒蛋白(VPg)的基因组预测

Genome prediction of putative genome-linked viral protein (VPg) of astroviruses.

作者信息

Al-Mutairy Badr, Walter Jolan E, Pothen Alex, Mitchell Douglas K

机构信息

Computer Science Department, Old Dominion University, Norfolk, Virginia 23529-0162, USA.

出版信息

Virus Genes. 2005 Aug;31(1):21-30. doi: 10.1007/s11262-004-2196-1.

Abstract

Positive-sense single-stranded RNA (+ssRNA) viruses replicate by uncoating the RNA genome for translation to provide viral proteins essential for genome replication and the production of new viral particles. The viral proteins are synthesized from a polyprotein precursor, which is cleaved nascently. The synthesized proteins include viral RNA-dependent RNA polymerase (RdRP), viral genome-linked protein (VPg), and a helicase. VPg is covalently attached to the genomic form of +ssRNA viruses. Helicases and NTPase unwind the RNA before replication. VPg and helicases have been identified in +ssRNA families, however, the presence of VPg and helicase in the Astroviridae, another +ssRNA family, has not been fully elucidated. Computational tools were utilized to provide sequence analysis evidence for the presence and genomic location of astrovirus VPg and helicase. HMMER program v2.1.1 was used to build Hidden Markov Model (HMM) profile for calicivirus VPg to search for conserved motifs in the astrovirus genome. We performed phylogenetic analysis of two genomic regions of astroviruses and caliciviruses (encoding the RdRP and VPg). We identified a putative VPg coding region in astrovirus. This region was located in open reading frame 1a (ORF1 a) and included sites with high sequence similarity to the VPg coding regions of Caliciviridae, Piconaviridae, and Potyviridae. A region encoding a putative astrovirus helicase identified conserved motifs only with pestivirus helicase sequences. Sequence analysis and comparison to other +ssRNA viruses supports the presence of VPg in the Astroviridae. Further laboratory analysis will be necessary to confirm these findings.

摘要

正链单链RNA(+ssRNA)病毒通过解开RNA基因组进行翻译来复制,以提供基因组复制和产生新病毒颗粒所必需的病毒蛋白。病毒蛋白由一个多蛋白前体合成,该前体在新生时被切割。合成的蛋白质包括病毒RNA依赖性RNA聚合酶(RdRP)、病毒基因组连接蛋白(VPg)和一种解旋酶。VPg共价连接到+ssRNA病毒的基因组形式上。解旋酶和NTPase在复制前解开RNA。VPg和解旋酶已在+ssRNA病毒科中被鉴定出来,然而,在另一个+ssRNA病毒科星状病毒科中VPg和解旋酶的存在尚未完全阐明。利用计算工具为星状病毒VPg和解旋酶的存在及基因组定位提供序列分析证据。使用HMMER程序v2.1.1构建杯状病毒VPg的隐马尔可夫模型(HMM)谱,以在星状病毒基因组中搜索保守基序。我们对星状病毒和杯状病毒的两个基因组区域(编码RdRP和VPg)进行了系统发育分析。我们在星状病毒中鉴定出一个假定的VPg编码区域。该区域位于开放阅读框1a(ORF1a)中,并且包含与杯状病毒科、小RNA病毒科和马铃薯Y病毒科的VPg编码区域具有高度序列相似性的位点。一个编码假定星状病毒解旋酶的区域仅与瘟病毒解旋酶序列鉴定出保守基序。序列分析以及与其他+ssRNA病毒的比较支持星状病毒科中存在VPg。需要进一步的实验室分析来证实这些发现。

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