Classical pathways of gene regulation by retinoids.

Cellular retinoic acid binding protein Genomic activity Nuclear co-repressor Retinoic acid receptor Retinoid X receptor Signaling

Journal

Methods in enzymology
ISSN: 1557-7988
Titre abrégé: Methods Enzymol
Pays: United States
ID NLM: 0212271

Informations de publication

Date de publication:
2020
Historique:
entrez: 4 5 2020
pubmed: 4 5 2020
medline: 24 6 2021
Statut: ppublish

Résumé

Retinoic acid receptors were discovered during early studies of the actions and mechanisms of essential vitamins. Vitamin A is metabolized in the body to retinoic acid (RA) which is a key compound in the control of many developmental processes in chordates. These functions are mediated by a subfamily of nuclear receptors, divided into two classes, the retinoic acid receptors (RAR) and the retinoid X receptors (RXR). Each class is encoded by three closely related genes that are located on different chromosomes. The three proteins in each class are designated α, β and γ, respectively. A wealth of structural studies have shown that they all share the same architecture including a DNA-binding domain connected by a flexible linker to the ligand and co-activator binding domain. Retinoic acid incorporation into the ligand-binding domain leads to a conformational change enabling the formation of RAR homodimers or RAR/RXR heterodimers that in turn bind specifically to target DNA sequences. The consensus sequences located on the promotors of regulated genes are known as retinoic acid response elements (RARE). The activated RAR/RXR homodimers recruit co-activators with histone acetylase activity leading to an opening of the chromatin structure and enabling downstream transcription of regulated genes. These canonical pathways describe the control mechanism for the majority of developmental processes mediated by retinoic acid and its derivatives.

Identifiants

pubmed: 32359644
pii: S0076-6879(20)30120-8
doi: 10.1016/bs.mie.2020.03.008
pii:
doi:

Substances chimiques

Receptors, Retinoic Acid 0
Retinoid X Receptors 0
Retinoids 0
Tretinoin 5688UTC01R

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

151-173

Subventions

Organisme : Medical Research Council
ID : MR/N0186481/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_17157
Pays : United Kingdom

Informations de copyright

© 2020 Elsevier Inc. All rights reserved.

Auteurs

Ehmke Pohl (E)

Department of Chemistry, Durham University, Durham, United Kingdom; Department of Bioscience, Durham University, Durham, United Kingdom; Biophysical Sciences Institute, Durham University, Durham, United Kingdom. Electronic address: ehmke.pohl@durham.ac.uk.

Charles W E Tomlinson (CWE)

Department of Chemistry, Durham University, Durham, United Kingdom.

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Classifications MeSH