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两种功能表征的树皮甲虫气味受体的假定配体结合位点。

Putative ligand binding sites of two functionally characterized bark beetle odorant receptors.

机构信息

Department of Biology, Lund University, SE-223 62, Lund, Sweden.

Division of Biochemistry and Structural Biology, Department of Chemistry, Lund University, SE-223 62, Lund, Sweden.

出版信息

BMC Biol. 2021 Jan 26;19(1):16. doi: 10.1186/s12915-020-00946-6.

DOI:10.1186/s12915-020-00946-6
PMID:33499862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7836466/
Abstract

BACKGROUND

Bark beetles are major pests of conifer forests, and their behavior is primarily mediated via olfaction. Targeting the odorant receptors (ORs) may thus provide avenues towards improved pest control. Such an approach requires information on the function of ORs and their interactions with ligands, which is also essential for understanding the functional evolution of these receptors. Hence, we aimed to identify a high-quality complement of ORs from the destructive spruce bark beetle Ips typographus (Coleoptera, Curculionidae, Scolytinae) and analyze their antennal expression and phylogenetic relationships with ORs from other beetles. Using 68 biologically relevant test compounds, we next aimed to functionally characterize ecologically important ORs, using two systems for heterologous expression. Our final aim was to gain insight into the ligand-OR interaction of the functionally characterized ORs, using a combination of computational and experimental methods.

RESULTS

We annotated 73 ORs from an antennal transcriptome of I. typographus and report the functional characterization of two ORs (ItypOR46 and ItypOR49), which are responsive to single enantiomers of the common bark beetle pheromone compounds ipsenol and ipsdienol, respectively. Their responses and antennal expression correlate with the specificities, localizations, and/or abundances of olfactory sensory neurons detecting these enantiomers. We use homology modeling and molecular docking to predict their binding sites. Our models reveal a likely binding cleft lined with residues that previously have been shown to affect the responses of insect ORs. Within this cleft, the active ligands are predicted to specifically interact with residues Tyr84 and Thr205 in ItypOR46. The suggested importance of these residues in the activation by ipsenol is experimentally supported through site-directed mutagenesis and functional testing, and hydrogen bonding appears key in pheromone binding.

CONCLUSIONS

The emerging insight into ligand binding in the two characterized ItypORs has a general importance for our understanding of the molecular and functional evolution of the insect OR gene family. Due to the ecological importance of the characterized receptors and widespread use of ipsenol and ipsdienol in bark beetle chemical communication, these ORs should be evaluated for their potential use in pest control and biosensors to detect bark beetle infestations.

摘要

背景

树皮甲虫是针叶林的主要害虫,它们的行为主要通过嗅觉来调节。因此,针对气味受体(ORs)可能为改善害虫防治提供途径。这种方法需要了解 ORs 的功能及其与配体的相互作用,这对于理解这些受体的功能进化也至关重要。因此,我们的目标是从破坏性的云杉树皮甲虫 Ips typographus(鞘翅目,象甲科,小蠹科)中鉴定出高质量的 OR 组合,并分析它们与其他甲虫 ORs 的触角表达和系统发育关系。接下来,我们使用 68 种具有生物学意义的测试化合物,旨在使用两种异源表达系统来对生态上重要的 OR 进行功能表征。我们的最终目标是使用计算和实验相结合的方法,深入了解功能表征的 ORs 的配体-OR 相互作用。

结果

我们从 I. typographus 的触角转录组中注释了 73 个 OR,并报告了两个 OR(ItypOR46 和 ItypOR49)的功能特征,它们分别对常见树皮甲虫信息素化合物 ipsenol 和 ipsdienol 的单一对映体有反应。它们的反应和触角表达与检测这些对映体的嗅觉感觉神经元的特异性、定位和/或丰度相关。我们使用同源建模和分子对接来预测它们的结合位点。我们的模型揭示了一个可能的结合裂隙,该裂隙由以前显示会影响昆虫 OR 反应的残基排列而成。在这个裂隙内,活性配体被预测与 ItypOR46 中的残基 Tyr84 和 Thr205 特异性相互作用。通过定点突变和功能测试,实验证实了这些残基在 ipsenol 激活中的重要性,氢键似乎是信息素结合的关键。

结论

在两个表征的 ItypOR 中对配体结合的深入了解对于我们理解昆虫 OR 基因家族的分子和功能进化具有普遍意义。由于所表征的受体具有生态重要性,以及 ipsenol 和 ipsdienol 在树皮甲虫化学通讯中的广泛使用,这些 OR 应该在害虫防治和用于检测树皮甲虫侵扰的生物传感器中进行评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/a5f716d75e51/12915_2020_946_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/c9362e9ea266/12915_2020_946_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/6e86745998fc/12915_2020_946_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/20543d65aa3f/12915_2020_946_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/0549abe36c49/12915_2020_946_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/01b14b0871a7/12915_2020_946_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/ef032b405792/12915_2020_946_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/a5f716d75e51/12915_2020_946_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/c9362e9ea266/12915_2020_946_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/6e86745998fc/12915_2020_946_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/d571575ee102/12915_2020_946_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/20543d65aa3f/12915_2020_946_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/0549abe36c49/12915_2020_946_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/01b14b0871a7/12915_2020_946_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/ef032b405792/12915_2020_946_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/512d/7836466/a5f716d75e51/12915_2020_946_Fig8_HTML.jpg

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