Tissue and Sex-Specific Transcriptomic Signatures Underlying Aggression behavior of Chinese Mitten Crab (Eriocheir sinensis)

IF 2.8 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jinliang Hou, Wenqi Zhao, Yongzhi Zhang, Xin Hou, Xiaowen Chen, Jun Wang, Chenghui Wang
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Abstract

Aggressive behavior is a critical constraint on sustainable crustacean aquaculture, causing cannibalism and yield loss. However, in the economically important Chinese mitten crab (Eriocheir sinensis), the molecular mechanisms underlying aggression responsiveness, particularly sex-specific regulation, remain poorly understood. Here, we used a standardized behavioral assay to quantify reactive aggression across three developmental stages and classified the quantified crabs into high-, moderate-, and low-aggression groups. Biochemical and transcriptomic profiling of the thoracic ganglion and the first pereiopod muscle were investigated to decode the mechanisms of aggression. High aggression was associated with significantly elevated catalase (CAT) activity and malondialdehyde (MDA) content, indicating increased oxidative stress that may reflect both the energetic demand of aggressive responses and the acute stress induced by the assay. Transcriptomic analyses showed that the upregulated genes in high-aggression crabs were enriched in neurotransmission and signal transduction pathways including dopaminergic, GABAergic, serotonergic, cAMP, and calcium signaling, which are consistent with altered neuromodulatory and signal-transduction capacity associated with high reactive aggression. Notably, significant enrichment of these neurotransmitter-related pathways was observed only in males, suggesting distinct sex-dependent adaptive strategies for aggressive behavior. Moreover, upregulated genes identified in the first pereiopod muscle of both females and males were mainly involved in metabolic processes, signal transduction, and immune defense pathways, indicating conserved functional roles across sexes. This study provides an integrative neurophysiological and transcriptomic framework for understanding the stimulus-induced aggressive response in Chinese mitten crab, highlighting oxidative trade-offs, tissue-specific regulation, and sex-dependent molecular strategies. These would help to conduct selective breeding and behavioral control in crustacean aquaculture.

中华绒螯蟹(Eriocheir sinensis)攻击行为的组织和性别特异性转录组特征
攻击行为是制约可持续甲壳类水产养殖的关键因素,会导致同类相食和产量损失。然而,在具有重要经济意义的中华绒螯蟹(Eriocheir sinensis)中,攻击反应的分子机制,特别是性别特异性调控机制仍然知之甚少。在这里,我们使用标准化的行为分析来量化三个发育阶段的反应性攻击,并将量化的螃蟹分为高、中、低攻击组。研究了胸神经节和第一视足肌的生化和转录组学分析,以解码攻击机制。高攻击性与过氧化氢酶(CAT)活性和丙二醛(MDA)含量显著升高相关,表明氧化应激增加可能反映了攻击反应的能量需求和实验诱导的急性应激。转录组学分析表明,高攻击性蟹的神经传递和信号转导通路中多巴胺能、gaba能、血清素能、cAMP和钙信号等基因表达上调,这与高攻击性蟹的神经调节和信号转导能力改变相一致。值得注意的是,这些神经递质相关通路的显著富集仅在雄性中观察到,这表明攻击行为的适应策略具有明显的性别依赖性。此外,在雌性和雄性第一表观足类肌肉中发现的上调基因主要参与代谢过程、信号转导和免疫防御途径,表明性别间的功能作用是保守的。本研究为理解中华绒螯蟹刺激诱导的攻击性反应提供了一个综合的神经生理学和转录组学框架,突出了氧化权衡、组织特异性调节和性别依赖的分子策略。这将有助于甲壳类水产养殖的选择性育种和行为控制。
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来源期刊
Marine Biotechnology
Marine Biotechnology 工程技术-海洋与淡水生物学
CiteScore
4.80
自引率
3.30%
发文量
95
审稿时长
2 months
期刊介绍: Marine Biotechnology welcomes high-quality research papers presenting novel data on the biotechnology of aquatic organisms. The journal publishes high quality papers in the areas of molecular biology, genomics, proteomics, cell biology, and biochemistry, and particularly encourages submissions of papers related to genome biology such as linkage mapping, large-scale gene discoveries, QTL analysis, physical mapping, and comparative and functional genome analysis. Papers on technological development and marine natural products should demonstrate innovation and novel applications.
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