Functional study and epigenetic targets analyses of SIRT1 in intramuscular preadipocytes via ChIP-seq and mRNA-seq

Epigenetics. 2023 Dec;18(1):2135194. doi: 10.1080/15592294.2022.2135194. Epub 2022 Oct 20.

Abstract

The SIRT1 epigenetic regulator is involved in hepatic lipid homoeostasis. However, the role of SIRT1 in regulating intramuscular fat deposition as well as the pathways and potential epigenetic targets involved remain unknown. Herein, we investigate SIRT1 function, its genome-wide epigenetic target profile, and transcriptomic changes under SIRT1 overexpression during yak intramuscular preadipocytes differentiation. To this end, we analysed the relationship between SIRT1 and intramuscular fat content as well as lipid metabolism-related genes in longissimus dorsi tissue. We found that SIRT1 expression negatively correlates with intramuscular fat content as well as with the expression of genes related to lipid synthesis, while positively correlating with that of fatty acid oxidation-involved genes. SIRT1 overexpression in intramuscular preadipocytes significantly reduced adipose differentiation marker expression, intracellular triacylglycerol content, and lipid deposition. Chromatin immunoprecipitation coupled with high-throughput sequencing of H3K4ac (a known direct target of SIRT1) and high-throughput mRNA sequencing results revealed that SIRT1 may regulate intramuscular fat deposition via three potential new transcription factors (NRF1, NKX3.1, and EGR1) and four genes (MAPK1, RXRA, AGPAT1, and HADH) implicated in protein processing within the endoplasmic reticulum pathway and the MAPK signalling pathway in yaks. Our study provides novel insights into the role of SIRT1 in regulating yak intramuscular fat deposition and may help clarify the mechanistic determinants of yak meat characteristics.

Keywords: H3K4ac; SIRT1; intramuscular fat deposition; intramuscular preadipocytes; yak.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue* / metabolism
  • Chromatin Immunoprecipitation Sequencing*
  • DNA Methylation
  • Epigenesis, Genetic
  • Lipids
  • RNA, Messenger / metabolism
  • Sirtuin 1 / metabolism

Substances

  • Sirtuin 1
  • Lipids
  • RNA, Messenger

Grants and funding

This work was supported by the National Natural Science Foundation of China [No.31902153];the Program of National Beef Cattle and Yak Industrial Technology System [No. CARS-37]; Fundamental Research Funds for the Central Universities, Southwest Minzu University [No. 2021114]; Natural Science Foundation of Sichuan Province [No. 2022NSFSC1716].