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美国白蛾核多角体病毒同源重复区的鉴定与特征分析

Identification and characterization of Hyphantria cunea nucleopolyhedrovirus homologous repeated regions.

作者信息

Alves Cristiano A Felipe, Ikeda Motoko, Kobayashi Michihiro

机构信息

Laboratory of Biodynamics, Graduate School of Bioagricultural Sciences, Nagoya University, 464-8601, Chikusa, Nagoya, Japan.

出版信息

Virus Genes. 2002 Dec;25(3):281-90. doi: 10.1023/a:1020928108541.

Abstract

A total of six homologous regions (hycu-hrs1-6) were identified in the genome of Hyphantria cunea nucleopolyhedrovirus (HycuNPV). These hycu-hrs were localized in non-coding regions interspersed throughout the HycuNPV genome and showed structural homology to several other baculovirus hrs. Sequence analyses indicated that hycu-hrs were composed of 65-69-bp direct repeats, each of which contained a 29-31-bp imperfect palindrome embedded within non-palindromes tandemly arranged. hycu-hrs consisted of a variable number of repeats ranging from two for hycu-hr3 to twenty-five for hycu-hr6, and these repeats showed a high degree of identity to each other. The hycu-hr6, which was localized immediately upstream of HycuNPV gp64 gene (hycu-gp64), represented the longest hr among group I NPV hrs reported to date. Transient expression assays demonstrated that the expression of hycu-gp64 promoter-driven luciferase gene (luc) was dramatically enhanced by hycu-hr6 which was placed upstream and downstream of luc in an orientation-independent manner. Moreover, hycu-hr6-dependent enhancement was observed in the absence of any additional viral gene products, although it could be further strengthened in the presence of HycuNPV ie-1 gene product. These results indicate that hycu-hrs function as enhancers of transcription mediated by RNA polymerase II, and suggest for the first time that efficiency of gp64 promoter is dependent on the enhancement function of hrs.

摘要

在舞毒蛾核型多角体病毒(HycuNPV)的基因组中总共鉴定出6个同源区域(hycu-hrs1-6)。这些hycu-hrs位于散布于HycuNPV基因组中的非编码区域,并且与其他几种杆状病毒的hrs具有结构同源性。序列分析表明,hycu-hrs由65 - 69个碱基对的直接重复序列组成,每个重复序列包含一个嵌入在串联排列的非回文序列中的29 - 31个碱基对的不完全回文序列。hycu-hrs由数量可变的重复序列组成,从hycu-hr3的2个到hycu-hr6的25个不等,并且这些重复序列彼此之间具有高度的同一性。位于HycuNPV gp64基因(hycu-gp64)紧邻上游的hycu-hr6是迄今为止报道的I组NPV hrs中最长的hr。瞬时表达分析表明,hycu-hr6以方向独立的方式置于luc基因的上游和下游时,可显著增强hycu-gp64启动子驱动的荧光素酶基因(luc)的表达。此外,在没有任何其他病毒基因产物的情况下也观察到了hycu-hr6依赖性增强,尽管在存在HycuNPV ie-1基因产物时这种增强作用会进一步加强。这些结果表明,hycu-hrs作为RNA聚合酶II介导的转录增强子发挥作用,并且首次表明gp64启动子的效率取决于hrs的增强功能。

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