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TCl4.7:一种在苹果蠹蛾颗粒体病毒中发现的新型鳞翅目转座子。

TCl4.7: a novel lepidopteran transposon found in Cydia pomonella granulosis virus.

作者信息

Jehle J A, Fritsch E, Nickel A, Huber J, Backhaus H

机构信息

Biologische Bundesanstalt für Land- und Forstwirtschaft, Institut für Biochemie und Pflanzenvirologie, Braunschweig, Germany.

出版信息

Virology. 1995 Mar 10;207(2):369-79. doi: 10.1006/viro.1995.1096.

Abstract

After the co-infection of larvae of the lepidopteran Cryptophlebia leucotreta with the two baculoviruses C. leucotreta granulosis virus and Cydia pomonella granulosis virus (CIGV and CpGV, respectively), three CpGV mutants and one CIGV mutant carrying insertions of 0.9 to 4.7 kb have been isolated. By cloning, sequencing, and hybridization analysis, one of these insertions was identified as a transposon-like element derived from the C. leucotreta genome. This element, called TCl4.7, was found in the genome of CpGV which naturally replicates in C. pomonella. Sequence analysis suggested that TCl4.7 is 4726 bp in size, flanked by imperfect inverted terminal repeats of 29 bp, and integrated into the target dinucleotide TA. TCl4.7 encompasses an open reading frame sharing homologies to transposase genes of the Tc1-related transposable elements found in Caenorhabditis and in Drosophila species. The open reading frame might represent a pseudogene since it is missing an ATG start codon. The integration site of TCl4.7 is located in a non-protein-coding region of the CpGV genome at m.u. 9.5. In bioassays the TCl4.7-carrying virus and all the other mutants except for one showed LC50 values similar to those of CpGV and CIGV. This is the first report of the horizontal escape of a transposable element during the in vivo infection of lepidopteran larvae by granulosis viruses.

摘要

鳞翅目害虫苹果小卷蛾(Cryptophlebia leucotreta)的幼虫被两种杆状病毒——苹果小卷蛾颗粒体病毒(C. leucotreta granulosis virus,CIGV)和苹果蠹蛾颗粒体病毒(Cydia pomonella granulosis virus,CpGV)共同感染后,已分离出三个携带0.9至4.7 kb插入片段的CpGV突变体和一个CIGV突变体。通过克隆、测序和杂交分析,其中一个插入片段被鉴定为源自苹果小卷蛾基因组的转座子样元件。这个元件被称为TCl4.7,它存在于在苹果蠹蛾中自然复制的CpGV基因组中。序列分析表明,TCl4.7大小为4726 bp,两侧是29 bp的不完全反向末端重复序列,并整合到靶标二核苷酸TA中。TCl4.7包含一个开放阅读框,与秀丽隐杆线虫和果蝇物种中发现的Tc1相关转座元件的转座酶基因具有同源性。由于缺少ATG起始密码子,该开放阅读框可能代表一个假基因。TCl4.7的整合位点位于CpGV基因组9.5 m.u.的非蛋白质编码区。在生物测定中,携带TCl4.7的病毒以及除一个之外的所有其他突变体的LC50值与CpGV和CIGV相似。这是关于颗粒体病毒在鳞翅目幼虫体内感染期间转座元件水平转移的首次报道。

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