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昆虫生物活性肽——生长阻滞肽的cDNA分子克隆与特性分析

Molecular cloning and characterization of cDNA for insect biogenic peptide, growth-blocking peptide.

作者信息

Hayakawa Y, Ohnishi A, Yamanaka A, Izumi S, Tomino S

机构信息

Institute of Low Temperature Science, Hokkaido University, Sapporo, Japan.

出版信息

FEBS Lett. 1995 Dec 4;376(3):185-9. doi: 10.1016/0014-5793(95)01273-7.

Abstract

Growth-blocking peptide (GBP) is an insect biogenic peptide that prevents the onset of metamorphosis from larva to pupa. A cDNA coding for GBP is described. Mixed oligonucleotides derived from a GBP peptide sequence were used to generate amplified DNA by the polymerase chain reaction (PCR). Based on the sequence of the amplified DNA, a 41 bases oligonucleotide was designed for screening a cDNA library which was constructed from the armyworm Pseudaletia separata larvae parasitized with the parasitic wasp Cotesia kariyai. The cloned cDNA for GBP was 809 base pairs in length. An open reading frame of 429 base pairs encodes a pre-pro-peptide of 143 amino acid residues in which GBP is localized at the C-terminal region, and other three peptides including a putative signal peptide and appropriate processing sites for endoproteolytic cleavage precede the GBP sequence. Northern blot analyses demonstrate the presence of a 800-base mRNA transcript in fat body and 2.5-kilobase transcript in brain and nerve cord, suggesting the possibility that the transcription of GBP gene is regulated in a tissue-dependent manner. This interpretation was supported by isolating a GBP cDNA fragment from cDNA pool of brain-nerve cords. GBP mRNA is constantly expressed in both parasitized and non-parasitized last instar larvae and there is no difference in the levels of the mRNA between both larvae, thus indicating that parasitism may effect on translational or posttranslational level to elevate plasma GBP concentration.

摘要

生长阻滞肽(GBP)是一种昆虫生物源肽,可阻止幼虫向蛹的变态发育。本文描述了编码GBP的cDNA。由GBP肽序列衍生而来的混合寡核苷酸用于通过聚合酶链反应(PCR)生成扩增DNA。根据扩增DNA的序列,设计了一个41个碱基的寡核苷酸用于筛选cDNA文库,该文库由被寄生蜂梨形环腹瘿蚊寄生的粘虫幼虫构建而成。克隆的GBP cDNA长度为809个碱基对。一个429个碱基对的开放阅读框编码一个由143个氨基酸残基组成的前原肽,其中GBP位于C端区域,在GBP序列之前还有其他三种肽,包括一个假定的信号肽和用于内切蛋白水解切割的合适加工位点。Northern印迹分析表明,在脂肪体中存在一个800碱基的mRNA转录本,在脑和神经索中存在一个2.5千碱基的转录本,这表明GBP基因的转录可能以组织依赖性方式受到调控。从脑-神经索的cDNA文库中分离出一个GBP cDNA片段,支持了这一解释。GBP mRNA在被寄生和未被寄生的末龄幼虫中均持续表达,且两种幼虫之间mRNA水平没有差异,因此表明寄生可能在翻译或翻译后水平上影响血浆GBP浓度的升高。

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