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与生化临床参数相关的肝脏代谢物和转录本的基因调控

Genetic Regulation of Liver Metabolites and Transcripts Linking to Biochemical-Clinical Parameters.

作者信息

Ponsuksili Siriluck, Trakooljul Nares, Hadlich Frieder, Methling Karen, Lalk Michael, Murani Eduard, Wimmers Klaus

机构信息

Leibniz Institute for Farm Animal Biology (FBN), Institute for Genome Biology, Functional Genome Analysis Research Unit, Dummerstorf, Germany.

Institute for Biochemistry - Metabolomics, University of Greifswald, Greifswald, Germany.

出版信息

Front Genet. 2019 Apr 17;10:348. doi: 10.3389/fgene.2019.00348. eCollection 2019.

Abstract

Given the central metabolic role of the liver, hepatic metabolites and transcripts reflect the organismal physiological state. Biochemical-clinical plasma biomarkers, hepatic metabolites, transcripts, and single nucleotide polymorphism (SNP) genotypes of some 300 pigs were integrated by weighted correlation networks and genome-wide association analyses. Network-based approaches of transcriptomic and metabolomics data revealed linked of transcripts and metabolites of the pentose phosphate pathway (PPP). This finding was evidenced by using a NADP/NADPH assay and and transcript quantification with the latter coding for first limiting enzyme of this pathway and by RNAi knockdown experiments of . Other transcripts including and showed link to amino acids and biomarkers. The amino acid metabolites were linked with transcripts of immune or acute phase response signaling, whereas the carbohydrate metabolites were highly enrich in cholesterol biosynthesis transcripts. Genome-wide association analyses revealed 180 metabolic quantitative trait loci (mQTL) ( < 10). Trans-4-hydroxy-L-proline ( = 6 × 10), being strongly correlated with plasma creatinine (CREA), showed strongest association with SNPs on chromosome 6 that had pleiotropic effects on expression as revealed by multivariate analysis. Consideration of shared marker association with biomarkers, metabolites, and transcripts revealed 144 SNPs associated with 44 metabolites and 69 transcripts that are correlated with each other, representing 176 mQTL and expression quantitative trait loci (eQTL). This is the first work to report genetic variants associated with liver metabolite and transcript levels as well as blood biochemical-clinical parameters in a healthy porcine model. The identified associations provide links between variation at the genome, transcriptome, and metabolome level molecules with clinically relevant phenotypes. This approach has the potential to detect novel biomarkers displaying individual variation and promoting predictive biology in medicine and animal breeding.

摘要

鉴于肝脏在代谢中的核心作用,肝脏代谢产物和转录本反映了机体的生理状态。通过加权相关网络和全基因组关联分析,整合了约300头猪的生化临床血浆生物标志物、肝脏代谢产物、转录本和单核苷酸多态性(SNP)基因型。基于网络的转录组学和代谢组学数据方法揭示了磷酸戊糖途径(PPP)的转录本和代谢产物之间的联系。使用NADP/NADPH测定法以及对该途径的第一个限速酶进行编码的转录本定量分析,以及通过RNA干扰敲低实验,证明了这一发现。其他转录本,包括……,显示出与氨基酸和生物标志物的联系。氨基酸代谢产物与免疫或急性期反应信号的转录本相关,而碳水化合物代谢产物在胆固醇生物合成转录本中高度富集。全基因组关联分析揭示了180个代谢定量性状位点(mQTL)(P < 10)。反式-4-羟基-L-脯氨酸(P = 6 × 10)与血浆肌酐(CREA)高度相关,与6号染色体上的SNP显示出最强的关联,多变量分析显示这些SNP对……的表达具有多效性。考虑与生物标志物、代谢产物和转录本共享的标记关联,发现144个SNP与44种代谢产物和69种相互关联的转录本相关,代表176个mQTL和表达定量性状位点(eQTL)。这是第一项在健康猪模型中报告与肝脏代谢产物和转录本水平以及血液生化临床参数相关的遗传变异的研究。所确定的关联提供了基因组、转录组和代谢组水平分子变异与临床相关表型之间的联系。这种方法有可能检测出显示个体差异的新型生物标志物,并促进医学和动物育种中的预测生物学发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b17c/6478805/0b3e0c808a9a/fgene-10-00348-g001.jpg

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