National Engineering Laboratory for Animal Breeding, China Agricultural University, No. 2 Yuanmingyuan West Rd., Beijing, 100193, China.
Tibet Agriculture and Animal Husbandry College, Linzhi, Tibet, 860000, China.
Sci Rep. 2017 Jun 16;7(1):3654. doi: 10.1038/s41598-017-03976-3.
Tibetan pigs that inhabit the Tibetan Plateau exhibit striking phenotypic and physiological differences from lowland pigs, and have adapted well to extreme conditions. However, the mechanisms involved in regulating gene expression at high altitude in these animals are not fully understood. In this study, we obtained transcriptomic and proteomic data from the heart tissues of Tibetan and Yorkshire pigs raised in the highlands (TH and YH) and lowlands (TL and YL) via RNA-seq and iTRAQ (isobaric tags for relative and absolute quantitation) analyses, respectively. Comparative analyses of TH vs. YH, TH vs.TL, TL vs. YL, and YH vs. YL yielded 299, 169, 242, and 368 differentially expressed genes (DEGs), and 473, 297, 394, and 297 differentially expressed proteins (DEPs), respectively. By functional annotation of these DEGs and DEPs, genes that were enriched in the HIF-1 signaling pathway (NPPA, ERK2, ENO3, and EGLN3), VEGF signaling pathway (ERK2, A2M, FGF1, CTGF, and DPP4), and hypoxia-related processes (CRYAB, EGLN3, TGFB2, DPP4, and ACE) were identified as important candidate genes for high-altitude adaptation in the Tibetan pig. This study enhances our understanding of the molecular mechanisms involved in hypoxic adaptation in pigs, and furthers our understanding of human hypoxic diseases.
栖息在青藏高原的藏猪表现出与低地猪明显不同的表型和生理特征,并且很好地适应了极端环境。然而,这些动物在高海拔环境下调节基因表达的机制尚不完全清楚。在这项研究中,我们通过 RNA-seq 和 iTRAQ(相对和绝对定量的同位素标记)分析,分别从高原(TH 和 YH)和低地(TL 和 YL)饲养的藏猪和约克夏猪的心脏组织中获得了转录组和蛋白质组数据。TH 与 YH、TH 与 TL、TL 与 YL 和 YH 与 YL 的比较分析分别产生了 299、169、242 和 368 个差异表达基因(DEGs),以及 473、297、394 和 297 个差异表达蛋白(DEPs)。通过对这些 DEGs 和 DEPs 的功能注释,鉴定出了在 HIF-1 信号通路(NPPA、ERK2、ENO3 和 EGLN3)、VEGF 信号通路(ERK2、A2M、FGF1、CTGF 和 DPP4)和缺氧相关过程(CRYAB、EGLN3、TGFB2、DPP4 和 ACE)中富集的基因,这些基因是藏猪适应高原的重要候选基因。这项研究增强了我们对猪缺氧适应相关分子机制的理解,并进一步加深了我们对人类缺氧性疾病的认识。