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Structural insights into the HNF4 biology

Hepatocyte Nuclear Factor 4 (HNF4) is a transcription factor (TF) belonging to the nuclear receptor (NR) family that is expressed in liver, kidney, intestine and pancreas. It is a master regulator of liver-specific gene expression, in particular those genes involved in lipid transport and glucose me...

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Autores principales: Beinsteiner, Brice, Billas, Isabelle M. L., Moras, Dino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315846/
https://www.ncbi.nlm.nih.gov/pubmed/37404310
http://dx.doi.org/10.3389/fendo.2023.1197063
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author Beinsteiner, Brice
Billas, Isabelle M. L.
Moras, Dino
author_facet Beinsteiner, Brice
Billas, Isabelle M. L.
Moras, Dino
author_sort Beinsteiner, Brice
collection PubMed
description Hepatocyte Nuclear Factor 4 (HNF4) is a transcription factor (TF) belonging to the nuclear receptor (NR) family that is expressed in liver, kidney, intestine and pancreas. It is a master regulator of liver-specific gene expression, in particular those genes involved in lipid transport and glucose metabolism and is crucial for the cellular differentiation during development. Dysregulation of HNF4 is linked to human diseases, such as type I diabetes (MODY1) and hemophilia. Here, we review the structures of the isolated HNF4 DNA binding domain (DBD) and ligand binding domain (LBD) and that of the multidomain receptor and compare them with the structures of other NRs. We will further discuss the biology of the HNF4α receptors from a structural perspective, in particular the effect of pathological mutations and of functionally critical post-translational modifications on the structure-function of the receptor.
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spelling pubmed-103158462023-07-04 Structural insights into the HNF4 biology Beinsteiner, Brice Billas, Isabelle M. L. Moras, Dino Front Endocrinol (Lausanne) Endocrinology Hepatocyte Nuclear Factor 4 (HNF4) is a transcription factor (TF) belonging to the nuclear receptor (NR) family that is expressed in liver, kidney, intestine and pancreas. It is a master regulator of liver-specific gene expression, in particular those genes involved in lipid transport and glucose metabolism and is crucial for the cellular differentiation during development. Dysregulation of HNF4 is linked to human diseases, such as type I diabetes (MODY1) and hemophilia. Here, we review the structures of the isolated HNF4 DNA binding domain (DBD) and ligand binding domain (LBD) and that of the multidomain receptor and compare them with the structures of other NRs. We will further discuss the biology of the HNF4α receptors from a structural perspective, in particular the effect of pathological mutations and of functionally critical post-translational modifications on the structure-function of the receptor. Frontiers Media S.A. 2023-06-19 /pmc/articles/PMC10315846/ /pubmed/37404310 http://dx.doi.org/10.3389/fendo.2023.1197063 Text en Copyright © 2023 Beinsteiner, Billas and Moras https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Beinsteiner, Brice
Billas, Isabelle M. L.
Moras, Dino
Structural insights into the HNF4 biology
title Structural insights into the HNF4 biology
title_full Structural insights into the HNF4 biology
title_fullStr Structural insights into the HNF4 biology
title_full_unstemmed Structural insights into the HNF4 biology
title_short Structural insights into the HNF4 biology
title_sort structural insights into the hnf4 biology
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315846/
https://www.ncbi.nlm.nih.gov/pubmed/37404310
http://dx.doi.org/10.3389/fendo.2023.1197063
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