LncRNA and Protein Expression Profiles Reveal Heart Adaptation to High-Altitude Hypoxia in Tibetan Sheep.
Zhaohua HeShaobin LiFangfang ZhaoHongxian SunJiang HuJiqing WangXiu LiuMingna LiSayed Haidar Abbas RazaYuzhu LuoPublished in: International journal of molecular sciences (2023)
The Tibetan sheep has an intricate mechanism of adaptation to low oxygen levels, which is influenced by both genetic and environmental factors. The heart plays a crucial role in the adaptation of Tibetan sheep to hypoxia. In the present study, we utilized transcriptomic and proteomic technologies to comprehensively analyze and identify the long non-coding RNAs (lncRNAs), genes, proteins, pathways, and gene ontology (GO) terms associated with hypoxic adaptation in Tibetan sheep at three different altitudes (2500 m, 3500 m, and 4500 m). By integrating the differentially expressed (DE) lncRNA target genes, differentially expressed proteins (DEPs), and differentially expressed genes (DEGs), we were able to identify and characterize the mechanisms underlying hypoxic adaptation in Tibetan sheep. Through this integration, we identified 41 shared genes/proteins, and functional enrichment analyses revealed their close association with lipid metabolism, glycolysis/gluconeogenesis, and angiogenesis. Additionally, significant enrichment was observed in important pathways such as the PPAR signaling pathway, glycolysis/gluconeogenesis, the oxoacid metabolic process, and angiogenesis. Furthermore, the co-expression network of lncRNAs and mRNAs demonstrated that lncRNAs (MSTRG.4748.1, ENSOART00020025894, and ENSOART00020036371) may play a pivotal role in the adaptation of Tibetan sheep to the hypoxic conditions of the plateau. In conclusion, this study expands the existing database of lncRNAs and proteins in Tibetan sheep, and these findings may serve as a reference for the prevention of altitude sickness in humans.
Keyphrases
- genome wide identification
- genome wide analysis
- genome wide
- long non coding rna
- endothelial cells
- poor prognosis
- signaling pathway
- transcription factor
- dna methylation
- heart failure
- bioinformatics analysis
- single cell
- network analysis
- copy number
- binding protein
- metabolic syndrome
- vascular endothelial growth factor
- emergency department
- epithelial mesenchymal transition
- type diabetes
- rna seq
- fatty acid
- oxidative stress
- endoplasmic reticulum stress
- amino acid
- cell proliferation
- small molecule