| Literature DB >> 29175243 |
Hwee Hui Lau1, Natasha Hui Jin Ng1, Larry Sai Weng Loo2, Joanita Binte Jasmen1, Adrian Kee Keong Teo3.
Abstract
The hepatocyte nuclear factors (HNFs) namely HNF1α/β, FOXA1/2/3, HNF4α/γ and ONECUT1/2 are expressed in a variety of tissues and organs, including the liver, pancreas and kidney. The spatial and temporal manner of HNF expression regulates embryonic development and subsequently the development of multiple tissues during adulthood. Though the HNFs were initially identified individually based on their roles in the liver, numerous studies have now revealed that the HNFs cross-regulate one another and exhibit synergistic relationships in the regulation of tissue development and function. The complex HNF transcriptional regulatory networks have largely been elucidated in rodent models, but less so in human biological systems. Several heterozygous mutations in these HNFs were found to cause diseases in humans but not in rodents, suggesting clear species-specific differences in mutational mechanisms that remain to be uncovered. In this review, we compare and contrast the expression patterns of the HNFs, the HNF cross-regulatory networks and how these liver-enriched transcription factors serve multiple functions in the liver and beyond, extending our focus to the pancreas and kidney. We also summarise the insights gained from both human and rodent studies of mutations in several HNFs that are known to lead to different disease conditions.Entities:
Keywords: Development; Disease; Hepatocyte nuclear factor; Liver; MODY; Regulatory network; Transcription
Mesh:
Substances:
Year: 2017 PMID: 29175243 DOI: 10.1016/j.jhep.2017.11.026
Source DB: PubMed Journal: J Hepatol ISSN: 0168-8278 Impact factor: 25.083