The retinoic acid receptor (RAR) is a type of nuclear receptor which can also act as a ligand-activated transcription factor[1] that is activated by both all-trans retinoic acid and 9-cis retinoic acid, retinoid active derivatives of Vitamin A.[2] They are typically found within the nucleus.[3] There are three retinoic acid receptors (RAR), RAR-alpha, RAR-beta, and RAR-gamma, encoded by the RARA, RARB, RARG genes, respectively. Within each RAR subtype there are various isoforms differing in their N-terminal region A.[1] Multiple splice variants have been identified in human RARs: four for RARA, five for RARB, and two for RARG.[4] As with other type II nuclear receptors, RAR heterodimerizes with RXR and in the absence of ligand, the RAR/RXR dimer binds to hormone response elements known as retinoic acid response elements (RAREs) complexed with corepressor protein. Binding of agonist ligands to RAR results in dissociation of corepressor and recruitment of coactivator protein that, in turn, promotes transcription of the downstream target gene into mRNA and eventually protein. In addition, the expression of RAR genes is under epigenetic regulation by promoter methylation.[5] Both the length and magnitude of the retinoid response is dependent of the degradation of RARs and RXRs through the ubiquitin-proteasome.[3] This degradation can lead to elongation of the DNA transcription through disruption of the initiation complex or to end the response to facilitate further transcriptional programs.[6] Due to RAR/RXR heterodimers acting as subtrates to the non steroid hormone ligand retinoid they are extensively involved in cell differentiation, proliferation, and apoptosis.
^ abBastien J, Rochette-Egly C (March 2004). "Nuclear retinoid receptors and the transcription of retinoid-target genes". Gene. 328: 1–16. doi:10.1016/j.gene.2003.12.005. PMID15019979.
^di Masi A, Leboffe L, De Marinis E, Pagano F, Cicconi L, Rochette-Egly C, et al. (February 2015). "Retinoic acid receptors: from molecular mechanisms to cancer therapy". Molecular Aspects of Medicine. 41: 1–115. doi:10.1016/j.mam.2014.12.003. PMID25543955.
^Bastien J, Rochette-Egly C (March 2004). "Nuclear retinoid receptors and the transcription of retinoid-target genes". Gene. 328: 1–16. doi:10.1016/j.gene.2003.12.005. PMID15019979.
