| 注册
首页|期刊导航|中国水产科学|杂交鳢与斑鳢早期发育的比较转录组分析及生长优势关键基因的筛选

杂交鳢与斑鳢早期发育的比较转录组分析及生长优势关键基因的筛选

刘佳骏 罗青 刘海洋 刘嘉峰 欧密 费树站 陈建华 赵建

中国水产科学2025,Vol.32Issue(12):1717-1733,17.
中国水产科学2025,Vol.32Issue(12):1717-1733,17.DOI:10.12264/JFSC2025-0191

杂交鳢与斑鳢早期发育的比较转录组分析及生长优势关键基因的筛选

Comparative transcriptomic analysis of Channa maculata and hybrid snakehead(C.maculata ♀×Channa argus ♂)during early development and screening of key growth-related genes

刘佳骏 1罗青 2刘海洋 2刘嘉峰 2欧密 2费树站 2陈建华 3赵建2

作者信息

  • 1. 江苏海洋大学海洋科学与水产学院,江苏省海洋生物技术重点实验室,江苏 连云港 222005||中国水产科学研究院珠江水产研究所,农业农村部热带亚热带水产种质资源利用与养殖重点实验室,广东 广州 510380
  • 2. 中国水产科学研究院珠江水产研究所,农业农村部热带亚热带水产种质资源利用与养殖重点实验室,广东 广州 510380
  • 3. 江苏海洋大学海洋科学与水产学院,江苏省海洋生物技术重点实验室,江苏 连云港 222005
  • 折叠

摘要

Abstract

Heterosis,or hybrid vigor,is a cornerstone of modern aquaculture;however,the molecular mechanisms underlying this phenomenon,particularly during the critical early developmental stages,remain poorly understood.Hybrid snakehead(Channa maculata ♀×C.argus ♂)displays marked growth superiority over its parents,making it an ideal model for dissecting the genetic basis of heterosis.In this study,we aimed to identify key regulatory genes and molecular pathways driving the early growth advantage in hybrid snakehead through comparative transcriptomic analysis against its maternal parent,C.maculata.Specifically,we constructed 12 cDNA libraries from whole-body samples at 13 days post-hatching(dph)and muscle tissues at 43 dph for both hybrid and parental groups.High-throughput RNA sequencing yielded approximately 500 million high-quality clean reads,with Q30 percentages consistently above 93.76%and mapping rates to the C.maculata reference genome(GCA_020496755.1)ranging from 68.73%to 95.90%,thereby confirming dataset reliability.Principal component analysis revealed distinct transcriptional profiles between hybrid and parental groups at both developmental stages,with the first principal component(PC1)accounting for 54.70%(13 dph)and 88.80%(43 dph)of total variance,indicating significant,stage-specific transcriptional reprogramming in the hybrid.Differential expression analysis,using a threshold of|log2(Fold Change)|≥1 and false discovery rate<0.05,identified 721 differentially expressed genes(DEGs;427 up-and 294 down-regulated)at 13 dph and 385 DEGs(168 up-and 217 down-regulated)at 43 dph in hybrid group.Venn analysis revealed 23 core DEGs shared between both stages,suggesting their sustained importance in growth regulation.Gene ontology enrichment analysis highlighted a dynamic shift in biological functions:at 13 dph,DEGs were predominantly enriched in foundational processes—such as"metabolic process,""cellular process,""binding,"and"catalytic activity"—suggesting an early metabolic priming for rapid growth in hybrid group;at 43 dph,the functional landscape significantly shifted towards"developmental process","multicellular organismal process",and"transporter activity",reflecting a transition to active tissue construction and morphological development.Kyoto Encyclopedia of Genes and Genomes pathway analysis further emphasized the enrichment of pathways associated with neuro-regulation,feeding behavior,muscle development,and energy metabolism.Ten core candidate genes,including npy,slc25a5,ugp2,obscn,ache,coro1ca,tuba,lmod2,nr4a1,and trim33,were selected,and their expression patterns were successfully validated via qPCR.Notably,the consistent upregulation of neuropeptide Y(npy),a potent appetite stimulator,suggests enhanced feeding motivation.Moreover,the upregulation of genes involved in energy metabolism,such as UDP-glucose pyrophosphorylase 2(ugp2)and solute carrier family 25 member 5(slc25a5),indicates an optimized energy supply chain for fueling growth.Concurrently,the downregulation of growth inhibitors—such as tripartite motif-containing 33(trim33)—may relieve myogenic inhibition.Furthermore,genes crucial for muscle structure and remodeling,including leiomodin-2(lmod2)and coronin-1A(coro1ca),showed differential expression,underscoring active muscle development.In conclusion,our findings demonstrate that early growth heterosis in hybrid snakehead is not governed by a single master gene but constitutes a complex trait orchestrated by the synergistic action of multiple genes across diverse biological pathways.We propose a model where enhanced neuroendocrine-driven feeding motivation,highly efficient energy metabolism,and accelerated muscle development collectively underpin growth superiority in hybrid group.Our findings provide novel insights into the molecular basis of fish heterosis and establish a scientific basis for marker-assisted selection,genetic improvement,and sustainable aquaculture of snakehead.

关键词

斑鳢/杂交鳢/早期发育/转录组/肌肉/杂交优势

Key words

Channa maculata/Channa maculata ♀×Channa argus ♂/early development/transcriptome/muscle/heterosis

分类

农业科技

引用本文复制引用

刘佳骏,罗青,刘海洋,刘嘉峰,欧密,费树站,陈建华,赵建..杂交鳢与斑鳢早期发育的比较转录组分析及生长优势关键基因的筛选[J].中国水产科学,2025,32(12):1717-1733,17.

基金项目

国家现代农业产业技术体系资助项目(CARS-46) (CARS-46)

广东省基础与应用基础研究基金项目(2024A1515030165). (2024A1515030165)

中国水产科学

OACSCD

1005-8737

访问量1
|
下载量0
段落导航相关论文