Animal Breeding and Genetics Program, Institute for Research and Technology in Food and Agriculture (IRTA), Torre Marimon, Caldes de Montbui, 08140, Spain.
Animal Genomics Department, Centre for Research in Agricultural Genomics (CRAG), Campus UAB, Bellaterra, 08193, Spain.
Sci Rep. 2018 Jan 11;8(1):558. doi: 10.1038/s41598-017-19072-5.
This study aims identifying candidate genes and pathways associated with feed efficiency (FE) in pigs. Liver and duodenum transcriptomes of 37 gilts showing high and low residual feed intake (RFI) were analysed by RNA-Seq. Gene expression data was explored through differential expression (DE) and weighted gene co-expression network analyses. DE analysis revealed 55 and 112 differentially regulated genes in liver and duodenum tissues, respectively. Clustering genes according to their connectivity resulted in 23 (liver) and 25 (duodenum) modules of genes with a co-expression pattern. Four modules, one in liver (with 444 co-expressed genes) and three in duodenum (gathering 37, 126 and 41 co-expressed genes), were significantly associated with FE indicators. Intra-module analyses revealed tissue-specific candidate genes; 12 of these genes were also identified as DE between individuals with high and low RFI. Pathways enriched by the list of genes showing DE and/or belonging to FE co-expressed modules included response to oxidative stress, inflammation, immune response, lipid metabolism and thermoregulation. Low overlapping between genes identified in duodenum and liver tissues was observed but heat shock proteins were associated to FE in both tissues. Our results suggest tissue-specific rather than common transcriptome regulatory processes associated with FE in pigs.
本研究旨在鉴定与猪饲料效率(FE)相关的候选基因和途径。通过 RNA-Seq 分析了表现出高和低剩余饲料摄入量(RFI)的 37 头母猪的肝脏和十二指肠转录组。通过差异表达(DE)和加权基因共表达网络分析探索了基因表达数据。DE 分析显示,肝脏和十二指肠组织中分别有 55 个和 112 个差异调节基因。根据它们的连接性对基因进行聚类,导致肝脏中有 23 个(肝脏)和 25 个(十二指肠)模块具有共表达模式。四个模块,一个在肝脏(有 444 个共表达基因)和三个在十二指肠(聚集 37、126 和 41 个共表达基因),与 FE 指标显著相关。模块内分析显示出组织特异性的候选基因;其中 12 个基因也被鉴定为高 RFI 和低 RFI 个体之间的 DE。显示 DE 和/或属于 FE 共表达模块的基因列表富集的途径包括对氧化应激、炎症、免疫反应、脂质代谢和体温调节的反应。在十二指肠和肝脏组织中鉴定的基因之间观察到的重叠很少,但热休克蛋白与两种组织中的 FE 相关。我们的研究结果表明,与猪 FE 相关的转录组调控过程是组织特异性的,而不是普遍的。