低温胁迫下吉富罗非鱼鳃的蛋白质组学分析

Proteomics analysis of gill tissue in GIFT tilapia(Oreochromis niloticus) under low temperature stress

  • 摘要: 【目的】 筛选出低温敏感型和低温耐受型吉富罗非鱼的鳃组织差异表达蛋白(DEPs),为揭示罗非鱼低温耐受分子机制提供理论基础,同时为培育低温抗性罗非鱼新品种(系)提供基础遗传资料。【方法】 采用同位素标记相对和绝对定量(iTRAQ)技术结合液相色谱串联质谱(LC-MS/MS)对低温胁迫前后的吉富罗非鱼鳃组织进行蛋白质组学分析,根据差异倍数(Fold Change)>1.3且P<0.05的筛选标准筛选出DEPs,然后进行GO功能注释分析和KEGG信号通路富集分析,并通过实时荧光定量PCR进行验证。【结果】 共鉴定出6603个蛋白,其中746个为DEPs(432个呈上调表达,314个呈下调表达)。GO功能注释分析发现,746个DEPs在生物学过程(BP)、细胞组分(CC)和分子功能(MF)三大功能类别中共注释到4772条GO功能条目。KEGG信号通路富集分析结果显示,746个DEPs分别富集到五大KEGG信号通路类别的31个亚群中,其中,免疫系统富集到115个DEPs(占15.4%),信号转导富集到88个DEPs(占11.8%),全局及概览图谱富集到75个DEPs(占10.1%);从富集程度来看,746个DEPs主要富集在肠道IgA免疫网络、造血细胞系、核糖体、补体和凝血级联反应等15条KEGG信号通路上。实时荧光定量PCR检测结果表明,包括C3C5在内的多个关键基因在低温耐受型吉富罗非鱼鳃组织中均呈明显下调表达趋势,尤其是C1qrsCD59C3C5C6Vtn等基因的表达极显著下调(P<0.01)。【结论】 低温胁迫后吉富罗非鱼鳃组织中的DEPs主要富集在肠道IgA免疫网络、造血细胞系及补体和凝血级联反应等与特异性/非特异性免疫、糖类代谢和脂质代谢相关的信号通路上,即鱼类免疫系统受抑制,对外界不利因素的抵抗能力下降,是低温环境胁迫下罗非鱼大批量死亡的主要原因。

     

    Abstract: 【Objective】 To screen differentially expressed proteins(DEPs) in gill tissues of low temperature sensitive and tolerant GIFT tilapia(Oreochromis niloticus), which could provide theoretical basis for exploring the molecular mechanisms of low temperature tolerance in tilapia, and offer basic genetic data for breeding new low temperature resistant GIFT tilapia varieties(lines). 【Method】 Isobaric tags for relative and absolute quantification(iTRAQ) technology combined with liquid chromatography-tandem mass spectrometry(LC-MS/MS) were used for proteomic analysis of gill tissues from GIFT tilapia before and after low temperature stress. DEPs were screened based on the criteria of Fold Change>1.3 and P<0.05, followed by GO functional annotation, KEGG signaling pathway enrichment analysis, and validation via real-time fluorescence quantitative PCR(qRT-PCR). 【Result】 A total of 6603 proteins were identified, including 746 DEPs(432 up-regulated and 314 down-regulated). GO functional annotation analysis showed that 746 DEPs were annotated to 4772 GO terms across 3 functional categories: biological process(BP), cellular component(CC) and molecular function(MF). KEGG signaling pathway enrichment analysis revealed that 746 DEPs were enriched in 31 subgroups of 5 KEGG pathways categories, with 115 DEPs(15.4%) in the immune system, 88 DEPs(11.8%) in signal transduction, and 75 DEPs(10.1%) in global and overview maps. In terms of enrichment degree, 746 DEPs were mainly enriched in 15 KEGG signaling pathways such as the intestinal IgA immune network, hematopoietic cell lines, ribosomes, complement and coagulation cascade response. qRT-PCR results showed that multiple key genes including C3 and C5 were greatly down-regulated in gill tissues of low temperature tolerant GIFT tilapia, especially the expression of C1qrs, CD59, C3, C5, C6 and Vtn genes extremely significantly down-regulated(P<0.01). 【Conclusion】 After low temperature stress, DEPs in gill tissues of GIFT tilapia are mainly enriched in pathways related to specific/non-specific immunity, carbohydrate metabolism, and lipid metabolism, such as intestinal IgA immune network, hematopoietic cell line, complement and coagulation cascade response. The suppression of the fish immune system and the decline in resistance to external adverse factors are the main causes of mass mortality in tilapia under low temperature stress.

     

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