低氧胁迫下缢蛏鳃转录组分析及能量代谢响应

Transcriptome analysis and energy metabolism response of gills of Sinonovacula constricta under hypoxia stress

  • 摘要: 【目的】 基于转录组测序分析低氧胁迫下缢蛏鳃组织的重要调控通路,探究低氧胁迫对缢蛏能量代谢相关基因的影响,以明确缢蛏应对低氧胁迫的响应机制。【方法】 对缢蛏进行低氧胁迫(溶解氧2.0±0.2 mg/L)12 h(L1)和24 h(L2),以常氧条件(溶解氧7.0±0.2 mg/L)为对照组(Control),采集缢蛏鳃组织进行转录组测序,筛选差异表达基因(DEGs)并进行KEGG信号通路富集分析。采用实时荧光定量PCR检测低氧胁迫0、4、8、12、24、48和96 h缢蛏鳃组织中能量代谢相关基因的相对表达量。【结果】 L1 vs Control比较组有5445个DEGs,L2 vs Control比较组有2980个DEGs。KEGG信号通路富集分析结果表明,L1 vs Control比较组共有498个上调DEGs注释到177条通路,显著(P<0.05,下同)富集的前10条通路包括钙信号通路、c GMP-PKG信号通路、C型凝集素受体信号通路等;L2 vs Control比较组共有583个上调DEGs注释到224条通路,其富集的代谢通路较L1 vs Control比较组增多,包括类固醇生物合成、亚油酸代谢、视黄醇代谢、泛醌和其他萜类醌的生物合成等通路。从L2 vs Control比较组DEGs中筛选出缢蛏鳃组织中响应低氧胁迫的能量代谢相关基因,主要涉及糖酵解/糖异生、TCA循环、AMPK信号通路、HIF-1信号通路等重要的调控通路。实时荧光定量PCR检测结果表明,随着低氧胁迫时间的延长,缢蛏鳃组织中己糖激酶基因(HK)、磷酸烯醇丙酮酸羧化激酶基因(PEPCK)、磷酸甘油酸激酶基因(PGK)的相对表达量呈先升高后降低再升高的变化趋势,在低氧胁迫4 h较0 h明显升高,且在低氧胁迫96 h呈高表达;葡萄糖转运蛋白-1基因(GLUT1)、烯醇化酶基因(ENO)的相对表达量在低氧胁迫4 h较0 h显著降低,在低氧胁迫12 h降至最低值,低氧胁迫持续24 h后GLUT1ENO基因的相对表达量逐渐上升,在低氧胁迫96 h达最高值且与0 h差异显著。【结论】 低氧胁迫促进缢蛏糖酵解/糖异生、HIF-1信号通路等调控通路中的基因上调,对缢蛏能量代谢存在显著影响,推测低氧胁迫下缢蛏通过糖酵解途径维持能量供应,PEPCKHKGLUT1PGK等基因参与能量代谢调节及低氧胁迫响应。

     

    Abstract: 【Objective】 To analyze the key regulatory pathways in the gill tissues of Sinonovacula constricta under hypoxia stress based on transcriptome sequencing and explore the effects of hypoxia stress on energy metabolism related genes, which could clarify the response mechanism of Sinonovacula constricta to hypoxia stress. 【Method】 Sinonovacula constricta were subjected to hypoxia stress with dissolved oxygen(DO) at 2.0±0.2 mg/L for 12 h(L1) and 24 h(L2), with a control group(Control) at normoxic conditions(DO 7.0±0.2 mg/L). Gill tissues were collected for transcriptome sequencing, followed by screening of differentially expressed genes(DEGs) and KEGG signaling pathway enrichment analysis. Real-time fluorescence quantitative PCR(qRT-PCR) was used to detect the relative expression of energy metabolism related genes in gill tissues under hypoxia stress at 0, 4, 8, 12, 24, 48 and 96 h. 【Result】 In the L1 vs Control group, 5445 DEGs were identified, and in the L2 vs Control group, 2980 DEGs were identified. KEGG enrichment analysis showed that 498 up-regulated DEGs in the L1 vs Control group were annotated to 177 pathways, with the top 10 significantly(P<0.05, the same below) enriched pathways including calcium signaling pathway, cGMP-PKG signaling pathway and C-type lectin receptor signaling pathway. In the L2 vs Control group, 583 up-regulated DEGs were annotated to 224 pathways, with an increase in enriched metabolic pathways compared to L1 vs Control group, including steroid biosynthesis, linoleic acid metabolism, retinol metabolism, ubiquinone and other terpenoid-quinone biosynthesis. Energy metabolism related genes in gill tissues responding to hypoxia stress were screened from DEGs in the L2 vs Control group, mainly involving key regulatory pathways such as glycolysis/gluconeogenesis, TCA cycle, AMPK signaling pathway and HIF-1 signaling pathway. qRT-PCR results showed that with prolonged hypoxic stress, the relative expression of hexokinase gene(HK), phosphoenolpyruvate carboxykinase gene(PEPCK), and phosphoglycerate kinase gene(PGK) first increased, then decreased, and then increased again, greatly increased at 4 h of hypoxia stress compared with 0 h, with high expression at 96 h. The relative expression of glucose transporter 1 gene(GLUT1) and enolase gene(ENO) significantly decreased at 4 h of hypoxia stress compared with 0 h, reached the lowest at 12 h, gradually increased after 24 h, and peaked at 96 h with significant differences from 0 h. 【Conclusion】 Hypoxia stress promotes the upregulation of genes in regulation pathways such as glycolysis/gluconeogenesis and HIF-1 signaling pathway, significantly affects energy metabolism in Sinvnovacula constricta. It is inferred that Sinvnovacula constricta maintains energy supply through the glycolytic pathway under hypoxia stress, and genes such as PEPCK, HK, GLUT1 and PGK are involved in energy metabolism regulation and hypoxia stress response.

     

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