蛋白质组学及其与转录组学的结合分析:牛磺酸对高脂喂养石斑鱼肝脏降脂的影响

Animals Pub Date : 2024-07-11 DOI:10.3390/ani14142039
Yu Zhou, Fakai Bai, Ruyi Xiao, Mingfan Chen, Yunzhang Sun, Jidan Ye
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引用次数: 0

摘要

为了了解牛磺酸对高脂肪摄入诱导的橙斑石斑鱼(Epinephelus coioides)肝脏脂肪沉积的干预效果,我们进行了蛋白质组分析,并与之前获得的转录组数据进行了关联分析。我们设计了三种含有两种脂肪水平的等蛋白(粗蛋白含量为 47%)日粮,分别命名为 10%脂肪日粮(10F)、15%脂肪日粮(15F)和 15%脂肪加 1%牛磺酸日粮(15FT)。10F 日粮作为对照日粮。饲喂 8 周后,15F 日粮的增重、饲料转化率和肝脏指数与 10F 日粮相当,但前者与后者相比增加了肝脏脂肪含量。与饲喂 15F 日粮相比,饲喂 15FT 日粮提高了增重,降低了饲料转化率、肝功能指数和肝脏脂肪含量。在比较15F组和15FT组的肝脏蛋白质组数据时,共鉴定出133个差异表达蛋白(DEPs),其中51个为上调DEPs,82个为下调DEPs。在这些差异表达蛋白中,进一步筛选出胆固醇27-羟化酶、磷脂酰磷酸酶LPIN、磷脂酰肌醇磷脂酶C和6-磷酸果糖-2-激酶等参与初级胆汁酸生物合成、甘油脂代谢、磷脂酰肌醇信号系统和AMPK信号通路的差异表达蛋白,它们是缓解高脂喂养鱼类肝脏牛磺酸脂肪沉积的关键差异表达蛋白。通过 KEGG 对转录组和蛋白质组数据的关联分析,3 个差异表达基因(atp1a、arf1_2 和 plcd)和 4 个 DEPs(CYP27α1、LPIN、PLCD 和 PTK2B)被共同富集到 5 个与脂肪代谢相关的通路中,包括初级胆汁酸合成、胆汁分泌、甘油脂代谢、磷脂 D 信号转导或/和磷脂肌醇信号转导。结果表明,膳食牛磺酸干预可激活胆汁酸的生物合成,抑制甘油三酯的生物合成,从而介导高脂喂养橙斑石斑鱼的肝脏降脂作用。本研究有助于深入了解膳食牛磺酸对高脂喂养石斑鱼的肝脏降脂作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomics and Its Combined Analysis with Transcriptomics: Liver Fat-Lowering Effect of Taurine in High-Fat Fed Grouper (Epinephelus coioides)
In order to understand the intervention effect of taurine on liver fat deposition induced by high fat intake in the orange-spotted grouper (Epinephelus coioides), we performed proteomic analysis and association analysis with previously obtained transcriptomic data. Three isoproteic (47% crude protein) diets were designed to contain two levels of fat and were named as the 10% fat diet (10F), 15% fat diet (15F), and 15% fat with 1% taurine (15FT). The 10F diet was used as the control diet. After 8 weeks of feeding, the 15F diet exhibited comparable weight gain, feed conversion ratio, and hepatosomatic index as the 10F diet, but the former increased liver fat content vs. the latter. Feeding with the 15FT diet resulted in an improvement in weight gain and a reduction in feed conversion ratio, hepatosomatic index, and liver fat content compared with feeding the 15F diet. When comparing liver proteomic data between the 15F and 15FT groups, a total of 133 differentially expressed proteins (DEPs) were identified, of which 51 were upregulated DEPs and 82 were downregulated DEPs. Among these DEPs, cholesterol 27-hydroxylase, phosphatidate phosphatase LPIN, phosphatidylinositol phospholipase C, and 6-phosphofructo-2-kinase were further screened out and were involved in primary bile acid biosynthesis, glycerolipid metabolism, the phosphatidylinositol signaling system, and the AMPK signaling pathway as key DEPs in terms of alleviating liver fat deposition of taurine in high-fat fed fish. With the association analysis of transcriptomic and proteomic data through KEGG, three differentially expressed genes (atp1a, arf1_2, and plcd) and four DEPs (CYP27α1, LPIN, PLCD, and PTK2B) were co-enriched into five pathways related to fat metabolism including primary bile acid synthesis, bile secretion, glycerolipid metabolism, phospholipid D signaling, or/and phosphatidylinositol signaling. The results showed that dietary taurine intervention could trigger activation of bile acid biosynthesis and inhibition of triglyceride biosynthesis, thereby mediating the liver fat-lowering effects in high-fat fed orange-spotted grouper. The present study contributes some novel insight into the liver fat-lowering effects of dietary taurine in high-fat fed groupers.
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