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黑森瘿蚊(Mayetiola destructor [Say])中类围食膜蛋白基因的cDNA克隆及转录表达

cDNA cloning and transcriptional expression of a peritrophin-like gene in the Hessian fly, Mayetiola destructor [Say].

作者信息

Mittapalli Omprakash, Sardesai Nagesh, Shukle Richard H

机构信息

Department of Entomology, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

Arch Insect Biochem Physiol. 2007 Jan;64(1):19-29. doi: 10.1002/arch.20157.

Abstract

One of the well-studied components of the insect gut is the peritrophic matrix (PM). This semipermeable structure primarily functions in digestion, and protection against invasive microorganisms and mechanical damage. We report the cDNA cloning and transcription profiles of a peritrophin-A like gene (designated MdesPERI-A1) in the Hessian fly Mayetiola destructor. The predicted amino acid sequence of MdesPERI-A1 revealed a putative secretion signal peptide at its amino terminus, similarity to peritrophins from other insects including dipterans, and the presence of two chitin binding domains each containing six cysteine residues. Quantitative expression analysis of MdesPERI-A1 mRNA in different larval tissues revealed the transcript to be predominantly present in the midgut (597.9-fold) compared to other tissues assayed including salivary glands and fat bodies. Spatial expression patterns during development showed a peak expression of MdesPERI-A1 in the feeding second-instars (146-fold) and a decline in expression in the pupal and adult stages. Transcription profiling of MdesPERI-A1 during compatible (larvae on susceptible plants) and incompatible (larvae on resistant plants) interactions with wheat revealed a greater level (1.7-fold) of MdesPERI-A1 transcript in larvae on resistant plants in the initial time point examined. However, MdesPERI-A1 expression declined in larvae on resistant plants at the later time points.

摘要

昆虫肠道中一个经过充分研究的组成部分是围食膜(PM)。这种半透性结构主要在消化过程中发挥作用,并能抵御入侵的微生物和机械损伤。我们报道了黑森瘿蚊Mayetiola destructor中一个类围食蛋白A基因(命名为MdesPERI-A1)的cDNA克隆及转录谱。MdesPERI-A1预测的氨基酸序列在其氨基末端显示出一个假定的分泌信号肽,与包括双翅目昆虫在内的其他昆虫的围食蛋白相似,并且存在两个几丁质结合结构域,每个结构域含有六个半胱氨酸残基。对MdesPERI-A1 mRNA在不同幼虫组织中的定量表达分析表明,与包括唾液腺和脂肪体在内的其他检测组织相比,该转录本主要存在于中肠(597.9倍)。发育过程中的空间表达模式显示,MdesPERI-A1在取食的二龄幼虫中表达量最高(146倍),在蛹期和成虫期表达量下降。在与小麦的亲和(幼虫取食感虫植物)和非亲和(幼虫取食抗性植物)互作过程中对MdesPERI-A1进行转录谱分析,发现在最初检测的时间点,抗性植物上的幼虫中MdesPERI-A1转录本水平更高(1.7倍)。然而,在随后的时间点,抗性植物上幼虫的MdesPERI-A1表达下降。

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