Transcriptome Reveals Molecular Mechanisms of Neuroendocrine Regulation of Allometric Growth in the Red Swamp Crayfish Procambarus clarkii

IF 2.6 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zheyan Chen, Yongqing Wang, Xianji Tao, Yihai Qiao, Xilei Li, Jianbin Feng, Jiale Li
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引用次数: 0

Abstract

Allometric growth is a typical characteristic of crustaceans, which mainly occurs among individuals, life stages, tissues, and between sexes. The red swamp crayfish Procambarus clarkii is an economically important crustacean species in the world. To date, the molecular regulatory mechanisms of neuroendocrine system in the allometric growth of P. clarkii remain unclear. In this study, P. clarkii exhibiting significant allometric growth among individuals were sampled from three full-sibling families. The brain, eyestalk, nerve cord, and Y-organ were dissected for transcriptome analysis. Key functional genes were identified by random forest and DESeq2 methods. The gene pathways were enriched utilizing Kyoto Encyclopedia Genes and Genomes (KEGG) analysis. Gene topological analysis was established through weighted gene co-expression network analysis (WGCNA), and hub genes were screened by protein–protein interaction (PPI) networks. Transcriptomic analysis results were validated via qRT-PCR. RNA-Seq identified 31 differentially expressed genes (DEGs) (7 up- and 24 downregulated); 301 DEGs (23 up- and 278 downregulated); 1308 DEGs (474 up- and 834 downregulated); and 64 DEGs (52 up- and 12 downregulated) in the brain, eyestalk, Y-organ, and nerve cord, respectively. Crucial functional genes such as CHIA in the brain and perlucin-like in the eyestalk were notably identified. WGCNA revealed two hub modules, while PPI networks identified neuroendocrine regulators module which hub genes mainly including CP1876-like and cuticle protein AM1199-like, and structural components module which hub genes mainly including CUB& CCP Domain-Containing Protein, ARRDC, and E3 Ubiquitin protein ligase MCYCBP2-like. Correspondingly, the significant gene pathways such as amino sugar and nucleotide sugar metabolism (pcla00520) and insect hormone biosynthesis (pcla00981) were enriched. The results revealed the complex interactions and regulatory relationships of hub genes within hub modules to coordinate molting and growth. The results of RNA-Seq analysis were validated by the consistency of gene expression in qRT-PCR. In present study, key functional genes in the neuroendocrine system regulating allometric growth among individuals were identified, and significant pathways mainly include hormone synthesis were screened, thus constructing a neuroendocrine molecular regulatory network for the allometric growth of P. clarkii. Building on these investigations, a comprehensive mechanism whereby neuroendocrine regulators interact with structural components to coordinate molting and growth was proposed. The result would provide valuable insights into the molecular regulatory mechanisms of allometric growth, highlighting the interplay between the neuroendocrine system and relevant tissues.

转录组揭示了克氏原螯虾神经内分泌调控异速生长的分子机制
异速生长是甲壳类动物的典型特征,主要发生在个体间、生命阶段间、组织间和两性间。克氏原螯虾(Procambarus clarkii)是世界上重要的经济甲壳类动物。迄今为止,神经内分泌系统在克氏杆菌异速生长中的分子调控机制尚不清楚。在本研究中,克氏杆菌在三个全同胞家庭中表现出显著的异速生长。解剖脑、眼柄、神经索和y型器官进行转录组分析。采用随机森林和DESeq2方法鉴定关键功能基因。利用京都百科基因与基因组(KEGG)分析对基因通路进行富集。通过加权基因共表达网络分析(WGCNA)建立基因拓扑分析,通过蛋白-蛋白相互作用网络(PPI)筛选枢纽基因。转录组学分析结果通过qRT-PCR验证。RNA-Seq鉴定出31个差异表达基因(DEGs)(7个上调,24个下调);301℃(23℃上调,278℃下调);1308℃(474℃上调,834℃下调);在脑、眼柄、y形器官和神经索中分别有64度(52度上调,12度下调)。关键的功能基因,如大脑中的CHIA和眼柄中的perlucin样基因得到了显著的鉴定。WGCNA发现了两个中枢模块,PPI网络发现了神经内分泌调节因子模块和结构成分模块,中枢基因主要包括CP1876-like和角质层蛋白AM1199-like;CCP结构域含蛋白,ARRDC和E3泛素蛋白连接酶mcycbp2样。相应的,氨基酸糖和核苷酸糖代谢(pcla00520)和昆虫激素生物合成(pcla00981)等重要基因通路也得到了丰富。研究结果揭示了轮毂基因在轮毂模块内的复杂相互作用和调控关系,以协调蜕皮和生长。qRT-PCR中基因表达的一致性验证了RNA-Seq分析的结果。本研究鉴定了个体间神经内分泌系统中调控异速生长的关键功能基因,筛选了以激素合成为主的重要途径,构建了克氏假杆菌异速生长的神经内分泌分子调控网络。在这些研究的基础上,提出了一种神经内分泌调节因子与结构成分相互作用以协调蜕皮和生长的综合机制。该结果将为异速生长的分子调控机制提供有价值的见解,突出了神经内分泌系统与相关组织之间的相互作用。
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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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