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机构地区:[1]浙江大学应用昆虫学研究所 [2]中国科学院上海生物化学研究所
出 处:《中国生物化学与分子生物学报》1999年第3期365-371,共7页Chinese Journal of Biochemistry and Molecular Biology
摘 要:茶尺蠖核型多角体病毒(EoSNPV)基因组的polh和egt基因区约14.2kb的酶切图谱被构建.egt基因位于polh基因上游约4.8kb处,但转录方向与polh基因相反.EcoRⅤ-L片段polh基因及其旁侧的1125核苷酸序列被测定.polh基因编码区长738核苷酸,可编码246氨基酸的多肽.起始密码子ATG上游是一个富含AT(AT占71.2%)的启动子区,在-52核苷酸处有杆状病毒晚期基因启动子转录起始基序ATAAG.在终止密码子下游208核苷酸有一个poly(A)信号,AATAAA.但EoSNPVpolh基因起始密码子ATG相邻核苷酸序列为GTAATGT,其-3是个G,这与已知的16种其它杆状病毒polh基因-3位置均是A不相同.在分析了EoSNPV和HaSNPV多角体蛋白基因核苷酸序列的基础上,通过MALIGN程序,比较了目前已发表的26种杆状病毒包涵体蛋白的序列,EoSNPV与黄杉毒蛾核型多角体病毒(OpSNPV)的同源性为最高,核苷酸序列的同源性为83.0%,氨基酸序列达94.7%;与其它20种鳞翅目NPV的同源性也很高,核苷酸序列同源性为72.6%~81.9%,氨基酸序列为83.7%~93?A restriction endonuclease map was constructed for the 14 2 kb polyhedrin gene region of Ectropis obliqua single enveloped nucleopolyhedrovirus (EoSNPV) genome.The ecdysteroid UDP glucosyl transferase ( egt ) gene was localized 4 8 kb upstream of the polyhedrin gene and transcribed in the opposite direction.A portion of the Eco RⅤ L fragment containing the polyhedrin gene was sequenced.An open reading frame of 738 nucleotides encoding a putative 246 amino acid polypeptide representing the polyhedrin gene was determined.A conserved ATAAG motif,associated with transcriptional start sites in other polyhedrin genes,was identified 51 nucleotides upstream of the EoSNPV polyhedrin gene.a putative polyadenylation signal,AATAAA,was found 208 nucleotides downstream of the termination codon.The sequence surrounding the start condon ATG in the polyhedrin gene was GTAATGT,with G at position 3 instead of A as in other NPV's polyhedrin genes.Phylogenetic analysis of the polyhedrin gene shows that EoSNPV is a member of the previously described lepidopteran NPV group Ⅱ and that it is most closely related to the polyhedrin gene of Orgyia pseudotsugata SNPV.
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