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基于转录组测序的高体鰤温度胁迫响应基因鉴定

利海萍 朱春华 田雅丽 李连成 龙宏沼 郝瑞娟 张冬英 茹笑影 邓秋霞 黄洋

南方农业学报2025,Vol.56Issue(6):1763-1774,12.
南方农业学报2025,Vol.56Issue(6):1763-1774,12.DOI:10.3969/j.issn.2095-1191.2025.06.007

基于转录组测序的高体鰤温度胁迫响应基因鉴定

Identification of temperature stress responsive genes in greater amberjack(Seriola dumerili)by transcriptome analysis

利海萍 1朱春华 1田雅丽 1李连成 1龙宏沼 1郝瑞娟 2张冬英 2茹笑影 2邓秋霞 2黄洋1

作者信息

  • 1. 广东海洋大学水产学院,广东 湛江 524088||南方海洋科学与工程广东省实验室(湛江),广东 湛江 524006
  • 2. 南方海洋科学与工程广东省实验室(湛江),广东 湛江 524006
  • 折叠

摘要

Abstract

[Objective]The aim of this study was to identify genes related to temperature stress response in greater am-berjack(Seriola dumerili)based on transcriptome sequencing,which could provide theoretical reference for exploring the mechanism of high temperature tolerance of Seriola dumerili and molecular mechanism of response to high tempera-ture stress.[Method]Seriola dumerili were selected as the research objects and divided into 25℃(T25),28℃(T28),31℃(T31)and 34℃(T34)groups according to the temperature setting.The Seriola dumerili juveniles in each group were raised under the corresponding temperature conditions for 7 d.On the 7th day of the experiment,6 Seriola dumerili juveniles were randomly selected from each group and intestinal tissues were collected.Total RNA from intestinal tissues was extracted using TRIzol reagent,cDNA library was constructed and transcriptome sequencing was performed using the Illumina NovaSeq 6000 platform.Differentially expressed genes(DEGs)were screened using DESeq2,and GO func-tional annotation and KEGG signaling pathway enrichment analysis were performed.Real-time fluorescence quantitative PCR was used to detect the relative expression levels of DEGs to verify the transcriptome results.[Result]All the juve-niles of Seriola dumerili in the T34 group died on the first day of feeding,indicating that they had a severe high tempera-ture stress response under this temperature.Transcriptome sequencing analysis showed that 5864.48,6506.81 and 5952.27 Mb high-quality bases and 39.40×106,43.67×106 and 39.93×106 high-quality sequences were obtained in the T25,T28 and T31 groups respectively.The average mapping rates of genes mapped to the genome of Seriola dumerili were 95.85%,95.80%and 95.79%respectively.DEGs screening results showed that a total of 2043 DEGs were obtained in the T25 vs T28 group and a total of 1218 DEGs were obtained in the T25 vs T31 group.Twelve and seven heat shock protein related DEGs were obtained in the T25 vs T28 and T25 vs T31 groups respectively,and ten and six DEGs were significantly up-regulated respectively(P<0.05).In addition,DEGs related to immune function and stress function were screened.GO functional annotation and enrichment analysis results showed that the DEGs in T25 vs T28 and T25 vs T31 groups were annotated to 3 functional categories:molecular function,cellular component and biological process.The DEGs in T25 vs T28 group were annotated to GO functional items such as small molecule metabolic process,organic acid metabolic process and small molecule biosynthesis process,and the DEGs in T25 vs T31 group were mainly annotated to GO functional items such as small molecule metabolic process,organic acid metabolic process and oxygen-containing acid metabolic process.KEGG signaling pathway enrichment analysis results showed that the DEGs in T25 vs T28 group were mainly enriched in signaling pathways such as proteasome,cysteine and methionine metabolism,and the DEGs in T25 vs T31 group were mainly enriched in signaling pathways such as endoplasmic reticulum protein processing,serine and threonine metabolism.Real-time fluorescence quantitative PCR detection verification results showed that the relative expression change trend of the 7 DEGs selected in T25 vs T28 and T25 vs T31 groups was basically consistent with the fragments per kilobase of exon model per million mapped fragments(FPKM)variation trend in transcriptome,indicating that the transcriptome data were reliable.[Conclusion]Under high temperature stress,Seriola dumerili effectively main-tains cellular protein homeostasis and redox balance by activating a molecular chaperone system centered on heat shock proteins and synergistically regulating the innate immune recognition signaling pathway and endoplasmic reticulum stress response.Seriola dumerili may have an adaptive mechanism to respond to temperature stress through a stress protein-immune recognition-endoplasmic reticulum repair synergistic network.

关键词

高体鰤/高温胁迫/热休克蛋白/免疫功能

Key words

Seriola dumerili/high temperature stress/heat shock protein/immune function

分类

农业科技

引用本文复制引用

利海萍,朱春华,田雅丽,李连成,龙宏沼,郝瑞娟,张冬英,茹笑影,邓秋霞,黄洋..基于转录组测序的高体鰤温度胁迫响应基因鉴定[J].南方农业学报,2025,56(6):1763-1774,12.

基金项目

海南省重大科技计划项目(ZDKJ2021011) (ZDKJ2021011)

广东海洋大学2023年校级第一批"揭榜挂帅"项目(030301022301) (030301022301)

广东省现代化海洋牧场适养品种核心技术攻关项目(2024-MRB-00-001) (2024-MRB-00-001)

南方海洋科学与工程广东省实验室(湛江)资助项目(ZJW-2023-10) Hainan Major Science and Technology Plan Project(ZDKJ2021011) (湛江)

The First Batch of"Unvei-ling and Leading"Project in 2023 of Guangdong Ocean University(030301022301) (030301022301)

The Core Technology Research Pro-ject for Suitable Breeding Species in Modern Marine Ranches in Guangdong(2024-MRB-00-001) (2024-MRB-00-001)

Project of Southern Marine Science and Engineering Guangdong Laboratory(Zhanjiang)(ZJW-2023-10) (Zhanjiang)

南方农业学报

OA北大核心

2095-1191

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