Sex-Biased Gene Expression of RNAi Pathway Components in the Sea Lice Caligus rogercresseyi

IF 2.8 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Alexandra Brante, Paulina Bustos, Paulina Schmitt, Rodolfo Farlora
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Abstract

RNA interference (RNAi) is a conserved mechanism for post-transcriptional gene regulation and a critical process of arthropod immunity. This study investigates RNAi-associated genes in Caligus rogercresseyi, an ectoparasitic sea louse that poses significant challenges to salmon aquaculture. In that regard, 16 RNAi-associated genes were identified by in silico analysis, including Cr-AGO1, Cr-CNOT1, Cr-DCR, Cr-SND1, and Cr-XRN1. Phylogenetic analysis demonstrated clustering with homologous sequences from other arthropods, particularly the ectoparasitic copepod Lepeophtheirus salmonis. RNA-Seq analyses revealed developmentally regulated expression patterns, with RNAi-associated genes clustered into four distinct expression profiles. Quantitative PCR (qPCR) validation confirmed significant male-biased expression for several key genes, including Cr-AGO1 (109-fold increase), Cr-DCR (22-fold), Cr-XRN1 (22-fold), Cr-SND1 (fourfold), and Cr-CNOT1 (threefold), suggesting potential roles in male reproductive processes such as spermatogenesis. Cr-DDX6, Cr-Drosha, and Cr-XPO5, potentially involved in oocyte development and RNA transport, exhibited female-biased expression. These results provide new insights into RNAi-associated gene expression in C. rogercresseyi, uncovering significant developmental and sex-biased expression patterns. Characterizing these critical genes establishes a foundation for exploring control strategies based on the RNAi process, targeting sex-biased and developmentally essential genes. Such treatments could reduce reproductive success in sea lice while minimizing environmental impact, offering a sustainable alternative for managing caligidosis in aquaculture.

Abstract Image

海虱RNAi通路组分的性别偏倚基因表达
RNA干扰(RNA interference, RNAi)是一种保守的转录后基因调控机制,是节肢动物免疫的关键过程。本研究调查了对鲑鱼养殖构成重大挑战的外寄生海虱Caligus rogercresseyi的rnai相关基因。在这方面,通过计算机分析鉴定了16个rnai相关基因,包括Cr-AGO1, Cr-CNOT1, Cr-DCR, Cr-SND1和Cr-XRN1。系统发育分析显示与其他节肢动物的同源序列聚类,特别是外寄生桡足动物Lepeophtheirus salmonis。RNA-Seq分析揭示了发育调节的表达模式,rnai相关基因聚集成四个不同的表达谱。定量PCR (qPCR)验证证实了几个关键基因的显著男性偏表达,包括Cr-AGO1(增加109倍),Cr-DCR(增加22倍),Cr-XRN1(增加22倍),Cr-SND1(增加4倍)和Cr-CNOT1(增加3倍),提示在男性生殖过程如精子发生中可能发挥作用。Cr-DDX6、Cr-Drosha和Cr-XPO5可能参与卵母细胞发育和RNA转运,表现出女性偏向性表达。这些结果为rnai相关基因在C. rogercresseyi中的表达提供了新的见解,揭示了显著的发育和性别偏倚的表达模式。表征这些关键基因为探索基于RNAi过程的控制策略,针对性别偏见和发育必需基因奠定了基础。这种处理方法可以降低海虱的繁殖成功率,同时最大限度地减少对环境的影响,为管理水产养殖中的石斑病提供可持续的替代办法。
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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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