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棉铃虫昆虫痘病毒(HaEPV)基因组图谱绘制以及编码HaEPV多角体蛋白和核苷三磷酸磷酸水解酶I蛋白的基因分析。

Mapping of the Heliothis armigera entomopoxvirus (HaEPV) genome, and analysis of genes encoding the HaEPV spheroidin and nucleoside triphosphate phosphohydrolase I proteins.

作者信息

Sriskantha A, Osborne R J, Dall D J

机构信息

CSIRO Division of Entomology, Canberra, Australia.

出版信息

J Gen Virol. 1997 Dec;78 ( Pt 12):3115-23. doi: 10.1099/0022-1317-78-12-3115.

Abstract

The genome of Heliothis armigera entomopoxvirus (HaEPV) has been mapped with four restriction endonuclease enzymes (BamHI, HindIII, PstI and XhoI), and its length estimated at 233 kbp. An EcoRI-generated HaEPV genomic fragment hybridized to all fragments identified as genomic termini, providing the first experimental evidence for the presence of terminal repeat elements in an EPV genome. The HaEPV spheroidin and nucleoside triphosphate phosphohydrolase I (NPHI) genes have been cloned and sequenced, and their deduced products shown to possess high levels of identity with homologues from other Genus B entomopoxviruses (EPVs). The genomic locations of these and other HaEPV genes and open reading frames have been determined; comparison of their locations with those of homologues in the Amsacta moorei EPV genome largely supports an hypothesis that the Genus B EPVs share a conserved genomic organization which differs from that of chordopoxviruses. It is proposed that genes of EPVs can be assigned to five actual or predicted homology-based groups, a categorization which is useful for directing and interpreting investigations of EPV gene functions and relationships.

摘要

棉铃虫昆虫痘病毒(HaEPV)的基因组已用四种限制性内切酶(BamHI、HindIII、PstI和XhoI)进行了图谱绘制,其长度估计为233千碱基对。一个由EcoRI产生的HaEPV基因组片段与所有被鉴定为基因组末端的片段杂交,为EPV基因组中存在末端重复元件提供了首个实验证据。HaEPV的多角体蛋白和核苷三磷酸磷酸水解酶I(NPHI)基因已被克隆和测序,其推导产物与其他B属昆虫痘病毒(EPV)的同源物具有高度同源性。这些以及其他HaEPV基因和开放阅读框的基因组位置已被确定;将它们的位置与摩尔粘虫痘病毒基因组中的同源物位置进行比较,在很大程度上支持了一个假说,即B属EPV共享一个与脊索痘病毒不同的保守基因组组织。有人提出,EPV的基因可分为五个实际的或基于预测同源性的组,这种分类有助于指导和解释对EPV基因功能及关系的研究。

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