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刘品, 王文博, 李超, 严少普, 李琪, 罗小敏, 张硕华, 张艺琛, 姚林荣. 急性氨氮胁迫下大口黑鲈的肝脏转录组特征分析[J]. 水生生物学报, 2024, 48(5): 713-724. DOI: 10.7541/2024.2023.0238
引用本文: 刘品, 王文博, 李超, 严少普, 李琪, 罗小敏, 张硕华, 张艺琛, 姚林荣. 急性氨氮胁迫下大口黑鲈的肝脏转录组特征分析[J]. 水生生物学报, 2024, 48(5): 713-724. DOI: 10.7541/2024.2023.0238
LIU Pin, WANG Wen-Bo, LI Chao, YAN Shao-Pu, LI Qi, LUO Xiao-Min, ZHANG Shuo-Hua, ZHANG Yi-Chen, YAO Lin-Rong. LIVER TRANSCRIPTOME OF LARGEMOUTH BASS (MICROPTERUS SAMOIDES) UNDER ACUTE AMMONIA NITROGEN STRESS[J]. ACTA HYDROBIOLOGICA SINICA, 2024, 48(5): 713-724. DOI: 10.7541/2024.2023.0238
Citation: LIU Pin, WANG Wen-Bo, LI Chao, YAN Shao-Pu, LI Qi, LUO Xiao-Min, ZHANG Shuo-Hua, ZHANG Yi-Chen, YAO Lin-Rong. LIVER TRANSCRIPTOME OF LARGEMOUTH BASS (MICROPTERUS SAMOIDES) UNDER ACUTE AMMONIA NITROGEN STRESS[J]. ACTA HYDROBIOLOGICA SINICA, 2024, 48(5): 713-724. DOI: 10.7541/2024.2023.0238

急性氨氮胁迫下大口黑鲈的肝脏转录组特征分析

LIVER TRANSCRIPTOME OF LARGEMOUTH BASS (MICROPTERUS SAMOIDES) UNDER ACUTE AMMONIA NITROGEN STRESS

  • 摘要: 为研究大口黑鲈(Micropterus salmoides)受到氨氮胁迫时基因表达的变化规律, 文章采用Illumina平台的HiSeq测序策略分析了氨氮胁迫12h和24h后大口黑鲈肝脏的基因表达谱。氨氮胁迫后在大口黑鲈肝脏共获得111.66 Gb的有效数据, 组装获得133486个单基因簇(Unigenes), N50为1000 bp。通过比较转录组分析在2个时间点共获得2072个差异表达基因, 其中氨氮胁迫12h获得1516个差异表达基因, 907个上调, 609个下调; 氨氮胁迫24h获得556个差异表达基因, 其中330个上调, 226个下调。GO功能注释分析结果表明, 在氨氮胁迫12h差异基因富集数目明显多于24h, 但在“氧化还原酶活性”条目中富集的差异基因数目则是氨氮胁迫24h多于12h。此外, KEGG功能富集分析发现, 氨氮胁迫对大口黑鲈肝脏氧化应激、细胞自噬和凋亡相关等途径产生影响。选取10个差异表达基因进行qPCR验证, 其表达水平与转录组差异基因分析结果一致, 证明了测序结果的可靠性。其中, 与氧化应激相关基因缺氧诱导因子1α (HIF1α)、生长停滞DNA损伤可诱导蛋白β (Gadd45β)、DNA损伤诱导转录因子4 (DDIT4)、与细胞自噬相关基因自噬微管相关蛋白轻链3 (LC3)及与细胞凋亡相关基因下游内质网氧化还原酶1α (Ero1α)在整个胁迫过程中均显著上调。综上所述, 氨氮胁迫能引起大口黑鲈肝脏氧化应激, 当机体调控作用不足时, 大口黑鲈通过细胞自噬与凋亡方式去除受损细胞, 以维持内环境稳定。研究结果将为进一步研究大口黑鲈在氨氮胁迫下生理调控的分子机制提供依据。

     

    Abstract: To understand the molecular mechanism of Micropterus salmoides subjected to ammonia nitrogen stress, the HiSeq sequencing strategy of Illumina platform was used to analyze the gene expression profiles in the liver of M. salmoides at 12h ammonia nitrogen stress (12h) and 24h ammonia stress (24h). We obtained 111.66 Gb of valid data and assembled a total of 133486 unigenes with N50 value of 1000 bp. Comparative transcriptional analysis identified 2072 differentially expressed genes (DEGs) at two time points. Specifically, 1516 DEGs were obtained at 12h, consisting of 907 up-regulated and 609 down-regulated genes, while 556 DEGs were obtained at 24h, with 330 up-regulated and 226 down-regulated. Gene ontology analysis revealed that the number of DEGs enriched at 12h was significantly higher than that at 24h, but there were more DEGs related to “Oxidoreductase activity” at 24h. In addition, KEGG enrichment analysis indicated that the DEGs were mainly involved in oxidative stress, autophagy and apoptosis related pathways. Subsequently, ten DEGs were selected for qPCR validation, and their expression levels were consistent with the sequencing analysis results, demonstrating the reliability of the sequencing data. Notably, the oxidative stress related gene Hypoxia-inducible factor 1 α (HIF1 α), Growth arrest DNA damage inducible protein 45β (Gadd45 β), DNA damage inducible transcript 4 (DDIT4), autophagy related gene microtubule-associated protein light chain 3 (LC3) and apoptosis downstream related gene endoplasmic reticulum oxidoreduclin1α (Ero1 α) displayed significant upregulated throughout the entire process of ammonia nitrogen stress. In summary, ammonia nitrogen stress could cause oxidative stress response in the liver of M. salmoides, while the damaged cells were eliminated by autophagy and apoptosis when the body’s regulatory role is insufficient to maintain internal environmental stability. The genes and pathways identified in this study will facilitate further investigations into the molecular mechanisms behind the tolerance of M. salmoides to ammonia stress.

     

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