飞蛾交配行为的可塑性和雄性竞争诱导的射精蛋白质组多样性

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY Journal of insect physiology Pub Date : 2024-07-01 DOI:10.1016/j.jinsphys.2024.104673
Zheng Yahong , Shi Lingping , Zhang Jing , Li Huixia , Wu Lingli , Zhao Qian
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摘要

在雄性竞争中,大而昂贵的射精是有利的。先前对木虱雄性附属腺分泌物的研究留下了一些悬而未决的问题,即雄性如何调节其交配行为和射精成分分配以应对不同程度的竞争。本研究旨在深入探讨这些尚未探索的方面。本研究鉴定了暴露于不同竞争条件下的雄性的928种射精蛋白质。值得注意的是,在非竞争、低竞争和高竞争条件下求偶的雄性分别表现出867、635和858种射精蛋白。在这些射精蛋白质中,约有 10%的蛋白质随着竞争强度的变化而变化。随后的分析集中于转移到雌性体内的蛋白质,结果发现44%的射精蛋白质被转移,其中37种蛋白质表现出差异表达。功能分析揭示了它们在精子成熟、运动和获能过程中的关键作用。我们的研究结果表明,作为对不同竞争水平的反应,木虱的射精蛋白丰度和传递发生了适应性调整。此外,荧光精子标记表明,在低竞争水平下,精子转移率较高,而精子长度较短。此外,有证据表明,雄性在面临竞争时会缩短求偶时间,延长交配时间。这些结果说明了竞争是如何驱动射精投资和行为可塑性的,为辅助生殖技术和害虫管理策略的进步提供了宝贵的启示。
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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Plasticity in moth mating behavior and ejaculate proteomic diversity induced by male competition

In male competition, large and costly ejaculates are advantageous. Prior research on male accessory gland secretions in Plutella xylostella left open questions about how males modulate their mating behaviors and ejaculate composition allocation in response to varying levels of competition. The current study aimed to delve deeper into these unexplored facets. A totally of 928 ejaculate proteins were identified across males exposed to different competition conditions. Notably, males courting under non–, low-, and high-competition scenarios exhibited 867, 635, and 858 ejaculate proteins, respectively. Approximately 10% of these ejaculate proteins displayed variations that aligned with changes in competition intensity. Subsequent analyses focused on the proteins transferred to females, revealing that 44% of ejaculate proteins were transferred, with 37 proteins exhibiting differential expression. Functional analyses uncovered their crucial roles in sperm maturation, motility, and capacitation. Our findings reveal adaptive adjustments in ejaculate protein abundance and transmission in P. xylostella as a response to varying competition levels. Moreover, fluorescent sperm labeling indicated higher sperm transfer during low competition correlated with shorter sperm length. Furthermore, evidence suggests that males shorten their courtship duration and extend their mating duration when faced with competition. These results illustrate how competition drives ejaculate investment and behavioral plasticity, offering valuable insights for advancements in assisted reproductive technologies and pest management strategies.

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来源期刊
Journal of insect physiology
Journal of insect physiology 生物-昆虫学
CiteScore
4.50
自引率
4.50%
发文量
77
审稿时长
57 days
期刊介绍: All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.
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