
doi: 10.1042/bst20140119
pmid: 25233423
Within nucleosomes, canonical histones package the genome, but they can be opportunely replaced with histone variants. The incorporation of histone variants into the nucleosome is a chief cellular strategy to regulate transcription and cellular metabolism. In pathological terms, cellular steatosis is an abnormal accumulation of lipids, which reflects impairment in the turnover of triacylglycerols, affecting any organ but mainly the liver. The present review aims to summarize the experimental evidence for histone variant functions in lipid metabolism.
CHROMATIN, H3.3, Epigenesis, Genetic, Histones, MATERNAL OBESITY, Non-alcoholic Fatty Liver Disease, lipid metabolism, BINDING, steatosis, Animals, Humans, Protein Isoforms, HEPATIC STEATOSIS, FATTY LIVER-DISEASE, histone variant, MACROH2A1, nucleosome, Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences, Lipid Metabolism, EPIGENETICS, Nucleosomes, GENOME, MICE, Alternative Splicing, Gene Expression Regulation, Liver, gene expression
CHROMATIN, H3.3, Epigenesis, Genetic, Histones, MATERNAL OBESITY, Non-alcoholic Fatty Liver Disease, lipid metabolism, BINDING, steatosis, Animals, Humans, Protein Isoforms, HEPATIC STEATOSIS, FATTY LIVER-DISEASE, histone variant, MACROH2A1, nucleosome, Radboudumc 11: Renal disorders RIMLS: Radboud Institute for Molecular Life Sciences, Lipid Metabolism, EPIGENETICS, Nucleosomes, GENOME, MICE, Alternative Splicing, Gene Expression Regulation, Liver, gene expression
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