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BDH1 acetylation at K116 modulates milk fat production in dairy goats
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作者 Tiantian Xiong Chong Chen +6 位作者 Xinglong Gong Chengming Han Min Tian Jun Luo Lu Deng Juan J.Loor Cong Li 《Journal of Animal Science and Biotechnology》 2026年第1期159-173,共15页
Background Goat milk is increasingly recognized for high digestibility and a distinctive compositional profile.Protein acetylation,an important post-translational modification,regulates biosynthetic and metabolic path... Background Goat milk is increasingly recognized for high digestibility and a distinctive compositional profile.Protein acetylation,an important post-translational modification,regulates biosynthetic and metabolic pathways.This study aimed to identify critical acetylated proteins and specific modification sites involved in milk production and component synthesis in dairy goats,thereby elucidating the molecular mechanisms of lactation.We performed a comparative TMT-based acetylomic and proteomic analysis of mammary tissues from Saanen dairy goats during peak lactation and the dry period using LC–MS/MS.A candidate acetylation site was further investigated in goat mammary epithelial cells(GMECs)through site-directed mutagenesis and lipid metabolic assays,establishing functional links between acetylation and mammary lipid metabolism and providing a foundation for molecular strategies to improve milk quality and yield.Results We established a comprehensive mammary acetylome,identifying 862 significantly acetylated proteins and 2,028 modification sites across the two physiological phases.Differentially acetylated proteins were predominantly localized to the cytoplasm(39.98%).From these,54 key acetylated proteins,including MTOR,BCAT2,QARS1,GOT1,GOT2,BDH1,ACSS1,STAT5B,FABP5,and GPAM were prioritized as candidates involved in milk protein synthesis,milk fat synthesis,lactose synthesis,and other lactation-related processes.Among them,β-hydroxybutyrate dehydrogenase 1(BDH1)acetylation was characterized in detail.Members of the HDAC family were identified as primary regulators mediating BDH1 deacetylation.BDH1 acetylation promoted lipid droplet formation and triglyceride synthesis in GMECs.At the transcriptional level,BDH1 acetylation upregulated LXRα,ACSL1 and SCD1,whereas deacetylation downregulated SCD1,FASN,and ACSL1.Notably,BDH1 acetylation/deacetylation significantly reduced SREBP1 expression,linking this modification to coordinated control of lipogenic gene networks.Conclusions This study established,for the first time,the comprehensive acetylome of mammary gland tissues in dairy goats,revealing a substantial number of differentially acetylated proteins and modification sites.We demonstrate that acetylation of BDH1 regulated by HDACs promotes lipid droplet biogenesis and triglyceride synthesis in GMECs through transcriptional modulation of key lipogenic genes and suppression of SREBP1.These findings provide mechanistic insights into the post-translational regulation of mammary lipid metabolism and offer molecular targets for future genetic and nutritional strategies aimed at enhancing milk quality and yield in dairy goats. 展开更多
关键词 Acetylome bdh1 protein Dairy goat Fat biosynthesis Modification sites
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肝细胞癌PD-1免疫治疗敏感性的靶基因分析
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作者 史宇泽 丁可 孙倍成 《安徽医科大学学报》 CAS 北大核心 2024年第8期1323-1329,1338,共8页
目的探究肝细胞癌(HCC)患者程序性死亡受体1(PD-1)免疫治疗敏感性的特征基因。方法通过加权基因共表达网络分析(WGCNA)及差异性分析筛选与PD-1免疫治疗敏感性相关数据集GSE202069及ERP117672中共同差异基因,将上述共同差异基因通过Lass... 目的探究肝细胞癌(HCC)患者程序性死亡受体1(PD-1)免疫治疗敏感性的特征基因。方法通过加权基因共表达网络分析(WGCNA)及差异性分析筛选与PD-1免疫治疗敏感性相关数据集GSE202069及ERP117672中共同差异基因,将上述共同差异基因通过Lasso回归筛选PD-1免疫治疗敏感性的特征基因;通过GEPIA及Ualcan数据库预测特征基因在HCC的表达水平,通过实时荧光定量反转录聚合酶链反应(RT-qPCR)、蛋白质印迹(WB)及免疫组织化学染色(IHC)实验验证其表达。构建过表达3-羟基丁酸脱氢酶1(BDH1)细胞系,通过肿瘤功能学实验细胞计数试剂盒8(CCK-8)、平板克隆、EdU染色、细胞划痕、Transwell实验探究其对肿瘤细胞增殖、迁移及侵袭能力的影响。结果通过WGCNA及差异性分析筛选出两项数据集共有118个共同差异基因,Lasso回归筛选出共同差异基因中与PD-1免疫治疗敏感性特征基因(含黄素二甲基苯胺单加氧酶3(FMO3),过氧化物酶体反式-2-烯酰辅酶A还原酶(PECR),BDH1,溶质载体家族7成员1(SLC7A1),细胞色素b5 A型(CYB5A)和磷酸烯醇丙酮酸羧激酶1(PCK1));生存分析表明BDH1与HCC最为相关(总体生存率:P<0.001;复发:P=0.007)。GEPIA及Ualcan数据库分析显示BDH1在HCC组织中低表达,通过RT-qPCR、WB及IHC对本中心收集的HCC样本进一步证实BDH1在HCC中低表达。CCK-8、平板克隆、EdU染色、细胞划痕、Transwell实验结果显示,与Hep3B pCDH组相比,过表达BDH1使得HCC细胞吸光度降低(t=4.766,P<0.01),克隆形成数目减少(t=16.02,P<0.0001),增殖细胞比例下降(t=23.13,P<0.0001),细胞迁移率减慢(t=25.28,P<0.0001),穿过小室数目减少(t=10.78,P=0.004)。结论BDH1是观察HCC患者PD-1免疫治疗敏感性的特征基因;BDH1具有抑制HCC细胞增殖、迁移和侵袭的能力。 展开更多
关键词 肝细胞癌 PD-1免疫治疗 bdh1 肿瘤功能学实验
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