Department of Animal & Food Sciences, University of Delaware, Newark, Delaware, United States of America.
PLoS One. 2022 Jul 1;17(7):e0269534. doi: 10.1371/journal.pone.0269534. eCollection 2022.
Feed efficiency (FE) is an important trait in the broiler industry due to its direct correlation to efficient muscle growth instead of fat deposition. The present study characterized and compared gene expression profiles in abdominal fat from broiler chickens of different FE levels to enhance the understanding of FE biology. Specifically, traditional whole-transcript RNA-sequencing (RNA-seq) and 3' UTR-sequencing (3' UTR-seq) were applied to 22 and 61 samples, respectively. Overall, these two sequencing techniques shared a high correlation (0.76) between normalized counts, although 3' UTR-seq showed a higher variance in sequencing and mapping performance statistics across samples and a lower rate of uniquely mapped reads. A higher percentage of 3' UTR-seq reads mapped to introns suggested the frequent presence of cleavage sites in introns, thus warranting future research to study its regulatory function. Differential expression analysis identified 1198 differentially expressed genes (DEGs) between high FE (HFE) and intermediate FE (IFE) chickens with False Discovery Rate < 0.05 and fold change > 1.2. The processes that were significantly enriched by the DEGs included extracellular matrix remodeling and mechanisms impacting gene expression at the transcriptional and translational levels. Gene ontology enrichment analysis suggested that the divergence in fat deposition and FE in broiler chickens could be associated with peroxisome and lipid metabolism possibly regulated by G0/G1 switch gene 2 (G0S2).
饲料效率(FE)是肉鸡产业中的一个重要特征,因为它与肌肉生长的效率直接相关,而不是脂肪沉积。本研究对不同 FE 水平的肉鸡腹部脂肪的基因表达谱进行了特征描述和比较,以增强对 FE 生物学的理解。具体来说,分别应用了传统的全转录组 RNA 测序(RNA-seq)和 3' UTR 测序(3' UTR-seq)对 22 和 61 个样本进行了分析。总的来说,这两种测序技术之间的归一化计数高度相关(0.76),尽管 3' UTR-seq 在测序和映射性能统计方面的样本间差异较大,且唯一映射读取率较低。更高比例的 3' UTR-seq 读取映射到内含子表明内含子中频繁存在切割位点,因此需要进一步研究其调节功能。差异表达分析鉴定出 HFE 和 IFE 肉鸡之间有 1198 个差异表达基因(DEGs),False Discovery Rate < 0.05,fold change > 1.2。DEGs 显著富集的过程包括细胞外基质重塑和影响转录和翻译水平基因表达的机制。GO 富集分析表明,肉鸡脂肪沉积和 FE 的差异可能与过氧化物酶体和脂质代谢有关,可能受 G0/G1 开关基因 2(G0S2)调控。