Alternative strategies based on transgenic Drosophila melanogaster for the functional characterization of insect Ionotropic Receptors.

IF 4.3 2区 生物学 Q1 BIOLOGY
Cristina M Crava, William B Walker, Alberto Maria Cattaneo
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引用次数: 0

Abstract

Background: Insect Ionotropic Receptors (IRs) are a relatively uncharted territory. Some studies have documented IR activation by recording neuronal activity in situ, others by their heterologous expression in Xenopus oocytes or mis-expressing IRs from Drosophila melanogaster or from the related D. sechellia into the D. melanogaster "ionotropic receptor decoder" neuron, which lacks the endogenous tuning receptor subunit but expresses IR-coreceptors.

Results: In this study, we first made use of Drosophila olfactory sensory neurons (OSNs) different from the "ionotropic receptor decoder", demonstrating that by replacing or introducing IRs alongside the native D. melanogaster ones, functional heteromeric complexes can be formed. IR41a1 from the lepidopteran Cydia pomonella exhibits binding to polyamines and the IR75d from the dipteran Drosophila suzukii binds hexanoic acid. Secondly, expressing D. suzukii's putative acid sensor IR64a into the "ionotropic receptor decoder" of D. melanogaster inhibits the response to the main activators of neighboring neurons from the same sensillum, despite that IR64a does not respond to acids. In situ hybridization on the antennae of D. suzukii unveils wide expression of IR64a in neurons proximal to the sacculus. Structural modeling analysis does not explain its absence of binding to acids; conversely, this approach identifies key amino acids features explaining the binding of hexanoic acid by IR75d. Finally, we have also explored alternative methods to heterologously express IRs based on Human Embryonic Kidney cells (HEK293). Despite observing correct expression of IRs in transfected cells through immunohistochemistry experiments, this approach did not achieve successful deorphanization of these receptors.

Conclusion: Our findings highlight the potential use of Drosophila OSNs as a valuable tool for functional characterization of IRs from different insect species: for the first time, we have provided evidence of IR-functionalities within alternative OSNs from the Drosophila's "ionotropic receptor decoder" neuron to functionally characterize and deorphanize IRs from lineages that are evolutionarily distant from the D. melanogaster subgroup, contributing to the understanding of chemosensory modalities in D. suzukii and C. pomonella, two globally significant agricultural pests. Additionally, the unsuccessful deorphanization in HEK cells highlights the complex requirements for IR functionality, supporting the use of Drosophila OSNs as a more suitable expression system.

基于转基因黑胃果蝇昆虫嗜离子受体功能表征的替代策略。
背景:昆虫嗜离子受体(IRs)是一个相对未知的领域。一些研究通过原位记录神经元活性来证明IR激活,另一些研究通过在非洲蟾卵细胞中异源表达或将来自黑腹果蝇或相关黑腹果蝇的IR错误表达到黑腹果蝇的“嗜离子受体解码器”神经元中来证明IR激活,该神经元缺乏内源性调节受体亚基,但表达IR辅助受体。结果:在本研究中,我们首次利用不同于“嗜离子受体解码器”的果蝇嗅觉感觉神经元(OSNs),证明通过替换或引入ir与天然果蝇嗅觉感觉神经元一起,可以形成功能性的异质复合物。鳞翅目Cydia pomonella的IR41a1与多胺结合,而来自双翅目果蝇suzukii的IR75d与己酸结合。其次,将铃木氏线虫假定的酸传感器IR64a表达到黑腹d.m anogaster的“嗜离子受体解码器”中,尽管IR64a对酸没有反应,但抑制了对来自同一感觉器的邻近神经元的主要激活剂的反应。对铃木氏夜蛾触角的原位杂交揭示了IR64a在小囊近端神经元中的广泛表达。结构模型分析不能解释其不与酸结合;相反,这种方法确定了解释IR75d与己酸结合的关键氨基酸特征。最后,我们还探索了基于人胚胎肾细胞(HEK293)异源表达IRs的替代方法。尽管通过免疫组织化学实验观察到转染细胞中IRs的正确表达,但这种方法并没有成功地实现这些受体的去孤儿化。结论:我们的研究结果突出了果蝇的生理活性因子作为一种有价值的工具,可以用于不同昆虫物种的生理活性因子的功能表征。我们首次在果蝇的“嗜离子受体解码器”神经元中提供了ir -功能的证据,以从功能上表征和去孤儿化来自进化上远离黑腹果蝇亚群的谱系的ir,有助于理解两种全球重要的农业害虫——苏氏弓形虫和pomonella的化学感觉模式。此外,HEK细胞中不成功的去孤儿化突出了对IR功能的复杂要求,支持使用果蝇OSNs作为更合适的表达系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biological Research
Biological Research 生物-生物学
CiteScore
10.10
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: Biological Research is an open access, peer-reviewed journal that encompasses diverse fields of experimental biology, such as biochemistry, bioinformatics, biotechnology, cell biology, cancer, chemical biology, developmental biology, evolutionary biology, genetics, genomics, immunology, marine biology, microbiology, molecular biology, neuroscience, plant biology, physiology, stem cell research, structural biology and systems biology.
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