The Landscape of Accessible Chromatin during Yak Adipocyte Differentiation.
Zhilong ZhangYongfeng ZhangQi BaoYarong GuChunnian LiangMin ChuXian GuoPengjia BaoPing YanPublished in: International journal of molecular sciences (2022)
Although significant advancement has been made in the study of adipogenesis, knowledge about how chromatin accessibility regulates yak adipogenesis is lacking. We here described genome-wide dynamic chromatin accessibility in preadipocytes and adipocytes by using the assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq), and thus revealed the unique characteristics of open chromatin during yak adipocyte differentiation. The chromatin accessibility of preadipocytes and adipocytes exhibited a similar genomic distribution, displaying a preferential location within the intergenic region, intron, and promoter. The pathway enrichment analysis identified that genes with differential chromatin accessibility were involved in adipogenic metabolism regulation pathways, such as the peroxisome proliferator activated receptor-γ (PPAR) signaling pathway, wingless-type MMTV integration site (Wnt) signaling pathway, and extracellular matrix-receptor (ECM-receptor) interaction. Integration of ATAC-seq and mRNA-seq revealed that genes with a high expression were associated with high levels of chromatin accessibility, especially within 1 kb upstream and downstream of the transcription start site. In addition, we identified a series of transcription factors (TFs) related to adipogenesis and created the TF regulatory network, providing the possible interactions between TFs during yak adipogenesis. This study is crucial for advancing the understanding of transcriptional regulatory mechanisms of adipogenesis and provides valuable information for understanding the adaptation of plateau species to high-altitude environments by maintaining whole body homeostasis through fat metabolism.
Keyphrases
- genome wide
- transcription factor
- dna methylation
- gene expression
- adipose tissue
- signaling pathway
- extracellular matrix
- copy number
- dna damage
- high fat diet induced
- insulin resistance
- dna binding
- genome wide identification
- stem cells
- binding protein
- pi k akt
- fatty acid
- epithelial mesenchymal transition
- type diabetes
- minimally invasive
- oxidative stress
- endoplasmic reticulum stress
- high throughput
- heat shock protein
- induced apoptosis
- health information