Retinoic acid receptors at 35 years.


Journal

Journal of molecular endocrinology
ISSN: 1479-6813
Titre abrégé: J Mol Endocrinol
Pays: England
ID NLM: 8902617

Informations de publication

Date de publication:
01 11 2022
Historique:
received: 30 05 2022
accepted: 26 07 2022
pubmed: 24 9 2022
medline: 13 10 2022
entrez: 23 9 2022
Statut: epublish

Résumé

For almost a century, vitamin A has been known as a nutrient critical for normal development, differentiation, and homeostasis; accordingly, there has been much interest in understanding its mechanism of action. This review is about the discovery of specific receptors for the vitamin A derivative, retinoic acid (RA), which launched extensive molecular, genetic, and structural investigations into these new members of the nuclear receptor superfamily of transcriptional regulators. These included two families of receptors, the RAR isotypes (α, β, and γ) along with three RXR isotypes (α, β, and γ), which bind as RXR/RAR heterodimers to cis-acting response elements of RA target genes to generate a high degree of complexity. Such studies have provided deep molecular insight into how the widespread pleiotropic effects of RA can be generated.

Identifiants

pubmed: 36149754
doi: 10.1530/JME-22-0097
doi:

Substances chimiques

Carrier Proteins 0
Receptors, Cytoplasmic and Nuclear 0
Receptors, Retinoic Acid 0
Retinoid X Receptors 0
Vitamin A 11103-57-4
Tretinoin 5688UTC01R

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

T13-T24

Auteurs

Martin Petkovich (M)

Department of Pathology and Molecular Medicine, Queens University, Kingston, Ontario, Canada.

Pierre Chambon (P)

Institut de Génétique et de Biologie Moléculaire et Cellulaire (I.G.B.M.C.), Illkirch, France.

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Classifications MeSH