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两个遗传群体中残余采食量表型不同的内洛尔牛肝脏转录组分析

Transcriptome Profiling of the Liver in Nellore Cattle Phenotypically Divergent for RFI in Two Genetic Groups.

作者信息

Serna-García Marta, Fonseca Larissa Fernanda Simielli, Panadero Romero Joaquin Javier, Carretero Asuncion Julian, Dos Santos Silva Danielly Beraldo, Salatta Bruna Maria, Frezarim Gabriela Bonfá, Mercadante Maria Eugênia Zerlotti, Bonilha Sarah Figueiredo Martins, Ferro Jesus Aparecido, De Albuquerque Lucia Galvão

机构信息

School of Agricultural and Veterinary Sciences, Sao Paulo State University (UNESP), Jaboticabal 14884-900, São Paulo, Brazil.

Igenomix S.L., 46021 Valencia, Spain.

出版信息

Animals (Basel). 2023 Jan 20;13(3):359. doi: 10.3390/ani13030359.

Abstract

The identification and selection of genetically superior animals for residual feed intake (RFI) could enhance productivity and minimize environmental impacts. The aim of this study was to use RNA-seq data to identify the differentially expressed genes (DEGs), known non-coding RNAs (ncRNAs), specific biomarkers and enriched biological processes associated with RFI of the liver in Nellore cattle in two genetic groups. In genetic group 1 (G1), 24 extreme RFI animals (12 low RFI (LRFI) versus 12 high RFI (HRFI)) were selected from a population of 60 Nellore bulls. The RNA-seq of the samples from their liver tissues was performed using an Illumina HiSeq 2000. In genetic group 2 (G2), 20 samples of liver tissue of Nellore bulls divergent for RFI (LRFI, = 10 versus HRFI, = 10) were selected from 83 animals. The raw data of the G2 were chosen from the ENA repository. A total of 1811 DEGs were found for the G1 and 2054 for the G2 (-value ≤ 0.05). We detected 88 common genes in both genetic groups, of which 33 were involved in the immune response and in blocking oxidative stress. In addition, seven (, , , , , , and ) possible gene biomarkers were identified through a receiver operating characteristic analysis (ROC) considering an AUC > 0.70. The gene was overexpressed in the LRFI group. This gene regulates the lipid metabolism protein turnover and inhibits cell death. We also found non-coding RNAs in both groups. MIR25 was up-regulated and SNORD16 was down-regulated in the LRFI for G1. For G2, up-regulated RNase_MRP and SCARNA10 were found. We highlight MIR25 as being able to act by blocking cytotoxicity and oxidative stress and RMRP as a blocker of mitochondrial damage. The biological pathways associated with RFI of the liver in Nellore cattle in the two genetic groups were for energy metabolism, protein turnover, redox homeostasis and the immune response. The common transcripts, biomarkers and metabolic pathways found in the two genetic groups make this unprecedented work even more relevant, since the results are valid for different herds raised in different ways. The results reinforce the biological importance of these known processes but also reveal new insights into the complexity of the liver tissue transcriptome of Nellore cattle.

摘要

识别和选择剩余采食量(RFI)遗传优势动物可以提高生产力并减少对环境的影响。本研究的目的是利用RNA测序数据,识别两个遗传组内婆罗门牛肝脏中与RFI相关的差异表达基因(DEGs)、已知非编码RNA(ncRNAs)、特定生物标志物以及富集的生物学过程。在遗传组1(G1)中,从60头婆罗门公牛群体中挑选出24头极端RFI动物(12头低RFI(LRFI)和12头高RFI(HRFI))。使用Illumina HiSeq 2000对其肝脏组织样本进行RNA测序。在遗传组2(G2)中,从83头动物中挑选出20份婆罗门公牛肝脏组织样本,这些样本在RFI方面存在差异(LRFI,n = 10;HRFI,n = 10)。G2的原始数据从欧洲核苷酸档案馆(ENA)数据库中选取。G1共发现1811个DEGs,G2共发现2054个DEGs(P值≤0.05)。我们在两个遗传组中检测到88个共同基因,其中33个参与免疫反应和阻止氧化应激。此外,通过考虑曲线下面积(AUC)> 0.70的受试者工作特征分析(ROC),鉴定出7个(, , , , , , )可能的基因生物标志物。 基因在LRFI组中过表达。该基因调节脂质代谢、蛋白质周转并抑制细胞死亡。我们还在两个组中发现了非编码RNA。在G1的LRFI中,MIR25上调,SNORD16下调。对于G2,发现RNase_MRP和SCARNA10上调。我们强调MIR25能够通过阻止细胞毒性和氧化应激发挥作用,而RMRP是线粒体损伤的阻断剂。两个遗传组内婆罗门牛肝脏中与RFI相关的生物学途径涉及能量代谢、蛋白质周转、氧化还原稳态和免疫反应。在两个遗传组中发现的共同转录本、生物标志物和代谢途径使这项前所未有的工作更具意义,因为这些结果对于以不同方式饲养的不同牛群都是有效的。这些结果强化了这些已知过程的生物学重要性,但也揭示了婆罗门牛肝脏组织转录组复杂性的新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed1c/9913155/27537646e754/animals-13-00359-g001.jpg

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