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
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
151-173Subventions
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.