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The molecular functions of hepatocyte nuclear factors - In and beyond the liver.
Lau, Hwee Hui; Ng, Natasha Hui Jin; Loo, Larry Sai Weng; Jasmen, Joanita Binte; Teo, Adrian Kee Keong.
Afiliação
  • Lau HH; Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology, Proteos, Singapore 138673, Singapore.
  • Ng NHJ; Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology, Proteos, Singapore 138673, Singapore.
  • Loo LSW; Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology, Proteos, Singapore 138673, Singapore; School of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore.
  • Jasmen JB; Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology, Proteos, Singapore 138673, Singapore.
  • Teo AKK; Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology, Proteos, Singapore 138673, Singapore; School of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore; Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapo
J Hepatol ; 68(5): 1033-1048, 2018 05.
Article em En | MEDLINE | ID: mdl-29175243
ABSTRACT
The hepatocyte nuclear factors (HNFs) namely HNF1α/ß, 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores Nucleares de Hepatócito / Fígado Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores Nucleares de Hepatócito / Fígado Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Singapura