Zhang Deyin, Zhang Xiaoxue, Li Fadi, Li Chong, La Yongfu, Mo Futao, Li Guoze, Zhang Yukun, Li Xiaolong, Song Qizhi, Zhao Yuan, Wang Weimin
College of Animal Science and Technology, Gansu Agricultural University, Lanzhou, China.
Engineering Laboratory of Sheep Breeding and Reproduction Biotechnology in Gansu Province, Minqin Zhongtian Sheep Industry Co. Ltd., Minqin, China.
Front Genet. 2019 Nov 19;10:1183. doi: 10.3389/fgene.2019.01183. eCollection 2019.
In the genetic improvement of livestock and poultry, residual feed intake (RFI) is an important economic trait. However, in sheep, the genetic regulatory mechanisms of RFI are unclear. In the present study, we measured the feed efficiency (FE)-related phenotypes of 137 male Hu lambs, and selected six lambs with very high (n = 3) and very low (n = 3) RFI values and analyzed their liver transcriptomes. A total of 101 differentially expressed genes were identified, of which 40 were upregulated and 61 were downregulated in the low-RFI group compared with that in the high-RFI group. The downregulated genes were mainly concentrated in immune function pathways, while the upregulated genes were mainly involved in energy metabolism pathways. Two differentially expressed genes, (encoding adrenoceptor alpha 2A) and (ryanodine receptor 2), were selected as candidate genes for FE and subjected to single nucleotide polymorphism scanning and association analysis. Two synonymous mutations, g.1429 C > A and 2 g.1117 A > C, were detected, which were both significantly associated with the feed conversion rate. These findings provide a deeper understanding of the molecular mechanisms regulating FE, and reveal key genes and genetic variants that could be used to genetically improve FE in sheep.
在家畜和家禽的遗传改良中,剩余采食量(RFI)是一个重要的经济性状。然而,在绵羊中,RFI的遗传调控机制尚不清楚。在本研究中,我们测量了137只雄性湖羊羔羊的饲料效率(FE)相关表型,并选择了6只RFI值非常高(n = 3)和非常低(n = 3)的羔羊,分析了它们的肝脏转录组。共鉴定出101个差异表达基因,与高RFI组相比,低RFI组中有40个基因上调,61个基因下调。下调的基因主要集中在免疫功能途径,而上调的基因主要参与能量代谢途径。选择两个差异表达基因(编码肾上腺素能受体α2A)和(兰尼碱受体2)作为FE的候选基因,并进行单核苷酸多态性扫描和关联分析。检测到两个同义突变,g.1429 C > A和2 g.1117 A > C,它们均与饲料转化率显著相关。这些发现为调控FE的分子机制提供了更深入的理解,并揭示了可用于绵羊FE遗传改良的关键基因和遗传变异。