Manzán María Alejandra, Lozano Mario E, Sciocco-Cap Alicia, Ghiringhelli Pablo D, Romanowski Víctor
Instituto de Bioquímica y Biología Molecular, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Argentina.
Virus Genes. 2002 Mar;24(2):119-30. doi: 10.1023/a:1014564331383.
The ecdysteroid UDP-glycosyltransferase (egt) gene of Epinotia aporema granulovirus (EpapGV) was cloned sequenced and its biological activity was assessed. It encodes a protein of 446 amino acids. Direct evidence that the cloned gene encodes an active EGT protein was obtained by transient expression assays in insect cells. The upstream untranslated region of the egt gene exhibits several consensus early promoter elements. Accordingly, the gene is expressed early upon infection of Epinotia aporema larvae and the EGT activity remains high until later times post infection. Sequence analyses indicate the presence of clusters of amino acid residues conserved among all the baculoviral EGTs, although their relation with proper protein folding, ligand binding and catalytic activity remain to be assessed. Phylogenetic trees consistently cluster the granulovirus EGTs separating them clearly from the nucleopolyhedroviruses.
克隆并测序了苹果蠹蛾颗粒体病毒(EpapGV)的蜕皮甾类UDP-糖基转移酶(egt)基因,并评估了其生物活性。它编码一种由446个氨基酸组成的蛋白质。通过在昆虫细胞中的瞬时表达试验,获得了克隆基因编码活性EGT蛋白的直接证据。egt基因的上游非翻译区表现出几个共有早期启动子元件。因此,该基因在苹果蠹蛾幼虫感染后早期表达,并且EGT活性在感染后较晚时间之前一直保持较高水平。序列分析表明,在所有杆状病毒EGT中存在氨基酸残基簇,尽管它们与正确的蛋白质折叠、配体结合和催化活性之间的关系仍有待评估。系统发育树始终将颗粒体病毒EGT聚类,将它们与核型多角体病毒清楚地分开。