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在一种对伪毒蛾致病的杆状病毒基因组中鉴定和表征一个假定的DNA复制起点。

Identification and characterization of a putative origin of DNA replication in the genome of a baculovirus pathogenic for Orgyia pseudotsugata.

作者信息

Pearson M N, Bjornson R M, Ahrens C, Rohrmann G F

机构信息

Department of Agricultural Chemistry, Agricultural & Life Sciences, Oregon State University, Corvallis 97331-7301.

出版信息

Virology. 1993 Dec;197(2):715-25. doi: 10.1006/viro.1993.1647.

Abstract

A four-kilobase (kb) region (HindIII-N, map units 7.0-11.3) of the Orgyia pseudotsugata multinucleocapsid nuclear polyhedrosis virus (OpMNPV) genome was found to contain sequences that conferred upon plasmids the ability to undergo infection-dependent replication. The plasmid DNA appeared to be replicated to form high molecular weight multimers. Plasmids with deletions of up to 1.8 kb from either end of the HindIII-N region were replication competent. However, a discrete sequence, contained within the region bracketed by the deletions, capable of specifying replication was not identified. No evidence for sequence homology was found between the OpMNPV HindIII-N region and regions elsewhere in the OpMNPV genome or to putative Autographa californica MNPV (AcMNPV) replication origins. Origin-dependent plasmid replication was shown to require the presence of the OpMNPV DNA polymerase gene. The OpMNPV origin replicated poorly in AcMNPV-infected Spodoptera frugiperda cells and, conversely, a putative AcMNPV origin (hr2) replicated at low levels in OpMNPV-infected Lymantria dispar cells.

摘要

人们发现,云杉芽卷叶蛾多核衣壳核型多角体病毒(OpMNPV)基因组的一个4千碱基(kb)区域(HindIII - N,图谱单位7.0 - 11.3)含有一些序列,这些序列赋予质粒依赖感染进行复制的能力。质粒DNA似乎被复制以形成高分子量多聚体。从HindIII - N区域两端缺失多达1.8 kb的质粒仍具有复制能力。然而,在缺失所界定区域内并未鉴定出一个能够指定复制的离散序列。在OpMNPV HindIII - N区域与OpMNPV基因组其他区域或假定的苜蓿银纹夜蛾核型多角体病毒(AcMNPV)复制起点之间未发现序列同源性证据。已证明依赖起点的质粒复制需要OpMNPV DNA聚合酶基因的存在。OpMNPV起点在感染AcMNPV的草地贪夜蛾细胞中复制效率很低,相反,一个假定的AcMNPV起点(hr2)在感染OpMNPV的舞毒蛾细胞中复制水平也很低。

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