AI Article Synopsis

  • RNA sequencing of Hu sheep and Tibetan sheep identified 2108 differentially expressed genes (DEGs), with 1247 downregulated and 861 upregulated, highlighting differences in fat tail characteristics.
  • GO and KEGG analyses showed these DEGs are involved in pathways related to adipocyte lipolysis and chemokine signaling.
  • Key genes like BMP2, HOXA11, PPP1CC, and LPIN1 play significant roles in regulating fat metabolism in sheep, providing potential targets for further research.

Article Abstract

Background: Hu sheep and Tibetan sheep in China are characterized by fat tails and thin tails, respectively. Several transcriptomes have been conducted in different sheep breeds to identify the differentially expressed genes (DEGs) underlying this trait. However, these studies identified different DEGs in different sheep breeds.

Results: Hence, RNA sequencing was performed on Hu sheep and Tibetan sheep. We obtained a total of 45.57 and 43.82 million sequencing reads, respectively. Two libraries mapped reads from 36.93 and 38.55 million reads after alignment to the reference sequences. 2108 DEGs were identified, including 1247 downregulated and 861 upregulated DEGs. GO and KEGG analyses of all DEGs demonstrated that pathways were enriched in the regulation of lipolysis in adipocytes and terms related to the chemokine signalling pathway, lysosomes, and glycosaminoglycan degradation. Eight genes were selected for validation by RT-qPCR. In addition, the transfection of BMP2 overexpression into preadipocytes resulted in increased PPAR-γ expression and expression. BMP2 potentially induces adipogenesis through LOX in preadipocytes. The number of lipid drops in BMP2 overexpression detected by oil red O staining was also greater than that in the negative control.

Conclusion: In summary, these results showed that significant genes (BMP2, HOXA11, PPP1CC and LPIN1) are involved in the regulation of adipogenesis metabolism and suggested novel insights into metabolic molecules in sheep fat tails.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9210821PMC
http://dx.doi.org/10.1186/s12864-022-08657-8DOI Listing

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