HNF4α isoforms: the fraternal twin master regulators of liver function

被引:6
|
作者
Radi, Sarah H. H. [1 ]
Vemuri, Kiranmayi [2 ,3 ]
Martinez-Lomeli, Jose [4 ]
Sladek, Frances M. M. [4 ]
机构
[1] Univ Calif Riverside, Dept Biochem, Riverside, CA 92521 USA
[2] Rutgers State Univ, Human Genet Inst New Jersey, Dept Genet, Piscataway, NJ USA
[3] Rutgers State Univ, Canc Inst New Jersey, New Brunswick, NJ USA
[4] Univ Calif Riverside, Dept Mol Cell & Syst Biol, Riverside, CA USA
来源
FRONTIERS IN ENDOCRINOLOGY | 2023年 / 14卷
基金
美国国家卫生研究院;
关键词
HNF4 & alpha; structure; isoforms; metabolism; liver; NUCLEAR FACTOR 4-ALPHA; LIGAND-BINDING DOMAIN; TRANSCRIPTION FACTOR; GENE-EXPRESSION; VISCERAL ENDODERM; HNF4-ALPHA GENE; FATTY-ACID; CYCLIN D1; ALPHA; RECEPTOR;
D O I
10.3389/fendo.2023.1226173
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the more than 30 years since the purification and cloning of Hepatocyte Nuclear Factor 4 (HNF4a), considerable insight into its role in liver function has been gleaned from its target genes and mouse experiments. HNF4a plays a key role in lipid and glucose metabolism and intersects with not just diabetes and circadian rhythms but also with liver cancer, although much remains to be elucidated about those interactions. Similarly, while we are beginning to elucidate the role of the isoforms expressed from its two promoters, we know little about the alternatively spliced variants in other portions of the protein and their impact on the 1000-plus HNF4a target genes. This review will address how HNF4a came to be called the master regulator of liver-specific gene expression with a focus on its role in basic metabolism, the contributions of the various isoforms and the intriguing intersection with the circadian clock.
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页数:14
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