Transcriptomic analysis reveals the hepatopancreas metabolic mechanisms of mud crab Scylla paramamosain fed diets with terrestrial animal fat sources replacing fish oil

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Comparative Biochemistry and Physiology D-Genomics & Proteomics Pub Date : 2025-02-04 DOI:10.1016/j.cbd.2025.101435
Jinjin Liu , Shihui Cui , Zihao Ye , Jing Chen , Mengyao Tang , Chaojia Chen , Yifang Xu , Ziyi Wang , Wei Yang , Ziping Zhang , Xuexi Wang
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Abstract

The transcriptome analysis following an 8-week feeding trial was employed to investigate the impacts of dietary terrestrial animal fats (TAFs includes lard oil (LO), beef tallow (BT) and poultry oil (PO)) replacing fish oil (FO) on the metabolic mechanism in hepatopancreas of mud crabs (Scylla paramamosain). The fatty acid (FA) transport, biosynthesis and lipid absorption and digestion were reduced through the regulation of PPAR pathway and the mRNA expressions of monoglyceride lipases (mgls), phosphatidate phosphatase-1 (pap1), acyl-sn-glycerol-3-phosphate acyltransferase delta (plcd), cAMP-dependent protein kinase catalytic (pkac), FA-binding protein 1 (fabp-1), FA transport protein 4 (fatp-4), short/branched chain specific acyl-CoA dehydrogenase (acdsb) and enoyl-CoA delta isomerase 2 (eci2), etc., after replacing FO with BT or LO. At the same time, dietary BT and LO regulated glycolysis, gluconeogenesis and insulin signals through increasing the genes of pyruvate dehydrogenase E1 (pdh), phosphoenolpyruvate carboxykinase (pepck) and phosphatidylinositol 3-kinase (pi3k) and regulated immunity status by down regulating the mRNA expressions of heat shock proteins 27 (hsp 27), cytochrome P450 (cyp 450), etc. Replacing FO with PO enhanced phospholipid storage, fat deposition, and inhibited glucose transport by up regulating pap1, mgls, lipin 1, lipinβ and down regulating glycosyl transferase (gt) and glucose transporter type 4 (glut4) expressions. The present study showed the signaling pathways and genes that were significantly regulated by TAFs replacing dietary FO, and revealed molecular mechanisms of TAFs in S. paramamosain. This would be conducive to the application of TAFs in aquatic feed.

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转录组学分析揭示了以陆源动物脂肪源替代鱼油饲料喂养的Scylla paramamosain泥蟹肝胰脏代谢机制
本试验采用8周饲养试验后的转录组分析方法,研究饲粮中陆生动物脂肪(TAFs包括猪油(LO)、牛油(BT)和家禽油(PO))替代鱼油(FO)对泥蟹(Scylla paramamosain)肝胰腺代谢机制的影响。通过调控PPAR通路,脂肪酸(FA)转运、生物合成和脂质吸收消化减少,单甘油酯脂肪酶(mgls)、磷脂磷酸酶-1 (pap1)、酰基- asn -甘油-3-磷酸酰基转移酶δ (plcd)、camp依赖性蛋白激酶催化(pac)、FA结合蛋白1 (fabp-1)、FA转运蛋白4 (fatp-4)、短链/支链特异性酰基- coa脱氢酶(acdsb)和烯基- coa δ异构酶2 (eci2) mRNA表达减少。等,用BT或LO代替FO后。同时,饲粮中添加BT和LO通过增加丙酮酸脱氢酶E1 (pdh)、磷酸烯醇丙酮酸羧激酶(pepck)和磷脂酰肌醇3-激酶(pi3k)基因来调节糖酵解、糖异生和胰岛素信号,并通过下调热休克蛋白27 (hsp 27)、细胞色素P450 (cyp 450)等mRNA表达来调节免疫状态。用PO代替FO增强磷脂储存、脂肪沉积,并通过上调pap1、mgls、lipin 1、lipinβ和下调糖基转移酶(gt)和葡萄糖转运蛋白4 (glut4)的表达抑制葡萄糖转运。本研究揭示了TAFs替代日粮鱼油显著调控的信号通路和基因,揭示了TAFs在S. paramamosain中的分子机制。这将有利于TAFs在水产饲料中的应用。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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