在非化学感觉组织中高度表达的OBP基因影响草地贪夜蛾的趋光性和繁殖。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wei-Kang Han, Feng-Xian Tang, Yang-Yang Yan, Yan Wang, Yi-Xi Zhang, Na Yu, Kan Wang, Ze-Wen Liu
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引用次数: 0

摘要

昆虫气味结合蛋白(OBPs)最初被认为是参与化学补偿的气味载体。然而,已经观察到越来越多的OBP基因表现出超出化学感觉组织的广泛表达模式。本文发现一个OBP基因(OBP31)在草地贪夜蛾幼虫的腹神经索、成年大脑和雄性生殖器官中高度表达。通过CRISPR/Cas9诱变产生了一株OBP31敲除菌株(OBP31-/-)。对于OBP31-/-,幼虫需要更长的化蛹时间,但OBP31--/-和野生型(WT)的蛹重没有差异。OBP31-/-幼虫表现出比WT幼虫更强的趋光性,表明OBP31在光感中的重要性。对于成虫的交配节律,OBP31-/-蛾表现出较早的第二次交配高峰。在OBP31-/-和WT蛾的杂交配对中,OBP31--/-组和OBP31+/-组的交配持续时间较长,孵化率较低♂ 与WT组相比。这些结果表明,OBP31在幼虫的光感和雄性生殖过程中发挥着至关重要的作用,并可为理解OBPs的生物学功能提供有价值的见解,而OBPs在化学感觉组织中并不具有特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An OBP gene highly expressed in non-chemosensory tissues affects the phototaxis and reproduction of Spodoptera frugiperda

An OBP gene highly expressed in non-chemosensory tissues affects the phototaxis and reproduction of Spodoptera frugiperda

Insect odorant binding proteins (OBPs) were initially regarded as carriers of the odorants involved in chemosensation. However, it had been observed that a growing number of OBP genes exhibited broad expression patterns beyond chemosensory tissues. Here, an OBP gene (OBP31) was found to be highly expressed in the larval ventral nerve cord, adult brain and male reproductive organ of Spodoptera frugiperda. An OBP31 knockout strain (OBP31−/−) was generated by CRISPR/Cas9 mutagenesis. For OBP31−/−, the larvae needed longer time to pupate, but there was no difference in the pupal weight between OBP31−/− and wild type (WT). OBP31−/− larvae showed stronger phototaxis than the WT larvae, indicating the importance of OBP31 in light perception. For mating rhythm of adults, OBP31−/− moths displayed an earlier second mating peak. In the cross-pairing of OBP31−/− and WT moths, the mating duration was longer, and hatchability was lower in OBP31−/− group and OBP31+/−♂ group than that in the WT group. These results suggested that OBP31 played a vital role in larval light perception and male reproductive process and could provide valuable insights into understanding the biological functions of OBPs that were not specific in chemosensory tissues.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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