Full text is available at the source.
Lysine Acetylation of CREBH Regulates Fasting-Induced Hepatic Lipid Metabolism
Modification of CREBH by Lysine Acetylation Controls Liver Fat Metabolism During Fasting
AI simplified
Abstract
Fasting induces acetylation of CREBH in mouse livers, which is crucial for its role in regulating lipid metabolism.
- CREBH is a transcription factor that plays a key role in maintaining energy balance in the liver.
- Acetylation of CREBH occurs in a time-dependent manner during fasting, affecting its transcriptional activity.
- The balance between acetylation by the enzyme PCAF and deacetylation by sirtuin-1 regulates the acetylation state of CREBH.
- The specific lysine residue at position 294 (K294) is essential for fasting-induced acetylation and subsequent gene activation.
- Mutations at K294 impact CREBH's ability to regulate target genes and can lead to conditions like hepatic steatosis and hyperlipidemia during prolonged fasting.
AI simplified