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犊牛补饲对断奶时F1安格斯×内洛尔杂交肉牛肌肉中与脂肪生成和脂质生成相关的基因表达、过程及信号通路的影响

Effect of Cow-Calf Supplementation on Gene Expression, Processes, and Pathways Related to Adipogenesis and Lipogenesis in Muscle of F1 Angus × Nellore Cattle at Weaning.

作者信息

Ramírez-Zamudio Germán Darío, Ganga Maria Júlia Generoso, Pereira Guilherme Luis, Nociti Ricardo Perecin, Chiaratti Marcos Roberto, Cooke Reinaldo Fernandes, Chardulo Luis Artur Loyola, Baldassini Welder Angelo, Machado-Neto Otávio Rodrigues, Curi Rogério Abdallah

机构信息

College of Animal Science and Food Engineering, São Paulo University (USP), Pirassununga 13635-900, SP, Brazil.

School of Agriculture and Veterinary Sciences (FCAV), São Paulo State University (UNESP), Jaboticabal 14884-900, SP, Brazil.

出版信息

Metabolites. 2023 Jan 21;13(2):160. doi: 10.3390/metabo13020160.

DOI:10.3390/metabo13020160
PMID:36837780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9962728/
Abstract

The aim of this study was to identify differentially expressed genes, biological processes, and metabolic pathways related to adipogenesis and lipogenesis in calves receiving different diets during the cow-calf phase. Forty-eight uncastrated F1 Angus × Nellore males were randomly assigned to two treatments from thirty days of age to weaning: no creep feeding (G1) or creep feeding (G2). The creep feed offered contained ground corn (44.8%), soybean meal (40.4%), and mineral core (14.8%), with 22% crude protein and 65% total digestible nutrients in dry matter. After weaning, the animals were feedlot finished for 180 days and fed a single diet containing 12.6% forage and 87.4% corn-based concentrate. muscle samples were collected by biopsy at weaning for transcriptome analysis and at slaughter for the measurement of intramuscular fat content (IMF) and marbling score (MS). Animals of G2 had 17.2% and 14.0% higher IMF and MS, respectively ( < 0.05). We identified 947 differentially expressed genes (log fold change 0.5, FDR 5%); of these, 504 were upregulated and 443 were downregulated in G2. Part of the genes upregulated in G2 were related to PPAR signaling (, , , and ), unsaturated fatty acid synthesis (, , , and ), and fatty acid metabolism (, , , and ). Regarding biological processes, the genes upregulated in G2 were related to cholesterol biosynthesis (, , , and ), unsaturated fatty acid biosynthesis (, , , and ), and insulin sensitivity ( and ). Cow-calf supplementation G2 positively affected energy metabolism and lipid biosynthesis, and thus favored the deposition of marbling fat during the postweaning period, which was shown here in an unprecedented way, by analyzing the transcriptome, genes, pathways, and enriched processes due to the use of creep feeding.

摘要

本研究的目的是鉴定在犊牛-母牛阶段接受不同日粮的犊牛中与脂肪生成和脂质生成相关的差异表达基因、生物学过程和代谢途径。48头未阉割的F1安格斯×内洛尔雄性犊牛从30日龄到断奶被随机分为两种处理:不补饲(G1)或补饲(G2)。提供的补饲饲料包含玉米粉(44.8%)、豆粕(40.4%)和矿物质核心料(14.8%),干物质中粗蛋白含量为22%,总可消化养分含量为65%。断奶后,动物在饲养场育肥180天,并饲喂一种含有12.6%粗饲料和87.4%玉米型精饲料的单一日粮。在断奶时通过活检采集肌肉样本用于转录组分析,并在屠宰时测量肌内脂肪含量(IMF)和大理石花纹评分(MS)。G2组动物的IMF和MS分别高出17.2%和14.0%(P<0.05)。我们鉴定出947个差异表达基因(log倍数变化>0.5,FDR<5%);其中,G2组中有504个上调,443个下调。G2组中上调的部分基因与PPAR信号传导(PPARA、PPARD、PPARG和PPARGC1A)、不饱和脂肪酸合成(FASN、SCD、ACSL1和ELOVL6)以及脂肪酸代谢(ACOX1、CPT1B、HADHA和LPL)有关。关于生物学过程,G2组中上调的基因与胆固醇生物合成(HMGCR、LSS、FDPS和SQLE)、不饱和脂肪酸生物合成(FASN、SCD、ACSL1和ELOVL6)以及胰岛素敏感性(INSR和IGF1)有关。犊牛-母牛阶段补饲G2对能量代谢和脂质生物合成有积极影响,因此有利于断奶后大理石花纹脂肪的沉积,通过分析转录组、基因、途径以及由于使用补饲而富集的过程,本研究以前所未有的方式展示了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/6dcb1c6e79bb/metabolites-13-00160-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/d53ccb0857fa/metabolites-13-00160-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/3c59785e0649/metabolites-13-00160-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/79d4db98b5e9/metabolites-13-00160-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/33d4bef0175a/metabolites-13-00160-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/d8d4b08685de/metabolites-13-00160-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/c0d2430aeb75/metabolites-13-00160-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/6dcb1c6e79bb/metabolites-13-00160-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/d53ccb0857fa/metabolites-13-00160-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/3c59785e0649/metabolites-13-00160-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/5407dfeed69b/metabolites-13-00160-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/79d4db98b5e9/metabolites-13-00160-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/33d4bef0175a/metabolites-13-00160-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/d8d4b08685de/metabolites-13-00160-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/c0d2430aeb75/metabolites-13-00160-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b4/9962728/6dcb1c6e79bb/metabolites-13-00160-g008.jpg

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