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RAR-related orphan receptor gamma

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(Redirected from LYC-55716)
RORC
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRORC, NR1F3, RORG, RZR-GAMMA, RZRG, TOR, RAR-related orphan receptor gamma, IMD42, RAR related orphan receptor C
External IDsOMIM: 602943; MGI: 104856; HomoloGene: 21051; GeneCards: RORC; OMA:RORC - orthologs
Orthologs
SpeciesHumanMouse
Entrez

6097

19885

Ensembl

ENSG00000143365

ENSMUSG00000028150

UniProt

P51449

P51450

RefSeq (mRNA)

NM_001001523
NM_005060

NM_001293734
NM_011281

RefSeq (protein)

NP_001001523
NP_005051

NP_001280663
NP_035411

Location (UCSC)Chr 1: 151.81 – 151.83 MbChr 3: 94.28 – 94.31 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

RAR-related orphan receptor gamma (RORγ) is a protein that in humans is encoded by the RORC (RAR-related orphan receptor C) gene.[5] RORγ is a member of the nuclear receptor family of transcription factors. It is mainly expressed in immune cells (Th17 cells) and it also regulates circadian rhythms. It may be involved in the progression of certain types of cancer.

Gene expression

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Two isoforms are produced from the same RORC gene,[6] probably by selection of alternative promoters.[7][8]

  • RORγ (also referred to as RORγ1) – produced from an mRNA containing exons 1 to 11.[9]
  • RORγt (also known as RORγ2) – produced from an mRNA identical to that of RORγ, except that the two 5'-most exons are replaced by an alternative exon, located downstream in the gene. This causes a different, shorter N-terminus.[7]

RORγ

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The mRNA of the first isoform, RORγ is expressed in many tissues, including thymus, lung, liver, kidney, muscle, and brown fat.[5][10][11] While RORγ mRNA is abundantly expressed, attempts to detect RORγ protein have not been successful; therefore it is not clear whether RORγ protein is actually expressed.[12] Consistent with this, the main phenotypes identified in RORγ-/- knockout mice (where neither isoform is expressed) are those associated with RORγt immune system function[13] and an isoform specific RORγt knockout displayed a phenotype identical to the RORγ-/- knockout.[13] On the other hand, circadian phenotypes of RORγ-/- mice[14] in tissues where the RORγt isoform is expressed in minute amounts argues for the expression of functional RORγ isoform. Absent protein in previous studies may be due to the high amplitude circadian rhythm of expression of this isoform in some tissues.

The mRNA is expressed in various peripheral tissues, either in a circadian fashion (e.g., in the liver and kidney) or constitutively (e.g., in the muscle).[15][16]

In contrast to other ROR genes, the RORC gene is not expressed in the central nervous system.

RORγt

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The second isoform, RORγt, is expressed in various immune cells. Of those, the most prominent examples are immature CD4+/CD8+ thymocytes, T helper 17 (Th17) cells and in type 3 innate lymphoid cells (ILC3). Mice lacking RORγt are devoid of lymph nodes and Peyer's patches due to the lack of Lymphoid tissue inducer cells (LTi), a subpopulation of ILC3s and important drivers of lymphoid organogenesis. [13][17][18][19] RORγt inhibitors are under development for the treatment of autoimmune diseases such as psoriasis and rheumatoid arthritis.[12][20]

Function

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The RORγ protein is a DNA-binding transcription factor and is a member of the NR1 subfamily of nuclear receptors.[21] Although the specific functions of this nuclear receptor have not been fully characterized yet, some roles emerge from the literature on the mouse gene.

Circadian rhythms

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The RORγ isoform appears to be involved in the regulation of circadian rhythms. This protein can bind to and activate the promoter of the ARNTL (BMAL1) gene,[15][22] a transcription factor central to the generation of physiological circadian rhythms. Also, since the levels of RORγ are rhythmic in some tissues (liver, kidney), it has been proposed to impose a circadian pattern of expression on a number of clock-controlled genes,[14] for example the cell cycle regulator p21.[23] Conversely, it has also been demonstrated that RORγt+ enteric ILC3s themselves are under circadian control, being entrained by light that is sensed by the suprachiasmatic nucleus. Importantly, the deletion of ARNTL in ILC3s using a RORc promoter disrupted enteric defence, reinforcing the role of clock machinery in the control of RORγt. Whilst ILC3s themselves oscillate in a circadian manner and exhibit diurnal variations in the expression of clock genes, it remains unclear exactly how the central clock relays these signals to the RORγt+ ILC3s in the gut.[24][25][26]

Immune regulation

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RORγt is the most studied of the two isoforms. Its best understood functionality is in the immune system. The transcription factor is essential for lymphoid organogenesis in the embryo, in particular lymph nodes and Peyer's patches, but not the spleen.[8][17][27] It is essential for the specific immune cells responsible for embryonic lymphoid formation, the Lymphoid Tissue inducer (LTi) cells.[13] Within these cells, retinoic acid induces expression of RORc. Consequently, removing the metabolic ground product for retinoic acid, vitamin A, from the diet of pregnant mice resulted in lower embryonic LTi cell differentiation, leading to smaller lymph nodes in the adult offspring and finally resulting in lower capabilities to clear a virus.[28] RORγt also plays an important regulatory role in thymopoiesis, by reducing apoptosis of thymocytes and promoting thymocyte differentiation into pro-inflammatory T helper 17 (Th17) cells.[17][27][29] It also plays a role in inhibiting apoptosis of undifferentiated T cells and promoting their differentiation into Th17 cells, possibly by down regulating the expression of Fas ligand and IL2, respectively .[6]

Despite the pro-inflammatory role of RORγt in the thymus, it is expressed in a Treg cell subpopulation in the colon, and is induced by symbiotic microflora. Abrogation of the gene's activity generally increases type 2 cytokines and may make mice more vulnerable to oxazolone-induced colitis.[30]

Cancer

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RORγ is expressed in certain subsets of cancer stem cells (EpCAM+/MSI2+) in pancreatic cancer and shows a strong correlation with tumor stage and lymph node invasion.[31] Amplification of the RORC gene has also been observed in other malignancies such as lung, breast and neuroendocrine prostate cancer.[31]

Ligands

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Intermediates within the cholesterol pathway have been shown to activate RORγt.[32] Various oxysterols are claimed to be an activator of RORγ, but with lower potency as cholesterol intermediates.[33][32]

As a drug target

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As antagonism of the RORγ receptor may have therapeutic applications in the treatment of inflammatory diseases, a number of synthetic RORγ receptor antagonists have been developed.[34]

Agonists may allow the immune system to combat cancer. LYC-55716 is an oral, selective RORγ (RORgamma) agonist in clinical trials on patients with solid tumors.[35][36]

See also

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References

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  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028150 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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  6. ^ a b He YW, Deftos ML, Ojala EW, Bevan MJ (December 1998). "RORgamma t, a novel isoform of an orphan receptor, negatively regulates Fas ligand expression and IL-2 production in T cells". Immunity. 9 (6): 797–806. doi:10.1016/S1074-7613(00)80645-7. PMC 2776668. PMID 9881970.
  7. ^ a b Villey I, de Chasseval R, de Villartay JP (December 1999). "RORgammaT, a thymus-specific isoform of the orphan nuclear receptor RORgamma / TOR, is up-regulated by signaling through the pre-T cell receptor and binds to the TEA promoter". European Journal of Immunology. 29 (12): 4072–4080. doi:10.1002/(SICI)1521-4141(199912)29:12<4072::AID-IMMU4072>3.0.CO;2-E. PMID 10602018.
  8. ^ a b Eberl G, Littman DR (October 2003). "The role of the nuclear hormone receptor RORgammat in the development of lymph nodes and Peyer's patches". Immunological Reviews. 195: 81–90. doi:10.1034/j.1600-065X.2003.00074.x. PMID 12969312. S2CID 18769627.
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  19. ^ Sawa S, Cherrier M, Lochner M, Satoh-Takayama N, Fehling HJ, Langa F, et al. (October 2010). "Lineage relationship analysis of RORgammat+ innate lymphoid cells". Science. 330 (6004): 665–669. Bibcode:2010Sci...330..665S. doi:10.1126/science.1194597. PMID 20929731. S2CID 206528599.
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  23. ^ Gréchez-Cassiau A, Rayet B, Guillaumond F, Teboul M, Delaunay F (February 2008). "The circadian clock component BMAL1 is a critical regulator of p21WAF1/CIP1 expression and hepatocyte proliferation". The Journal of Biological Chemistry. 283 (8): 4535–4542. doi:10.1074/jbc.M705576200. PMID 18086663.
  24. ^ Godinho-Silva C, Domingues RG, Rendas M, Raposo B, Ribeiro H, da Silva JA, et al. (October 2019). "Light-entrained and brain-tuned circadian circuits regulate ILC3s and gut homeostasis". Nature. 574 (7777): 254–258. Bibcode:2019Natur.574..254G. doi:10.1038/s41586-019-1579-3. PMC 6788927. PMID 31534216.
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  27. ^ a b Kurebayashi S, Ueda E, Sakaue M, Patel DD, Medvedev A, Zhang F, Jetten AM (August 2000). "Retinoid-related orphan receptor gamma (RORgamma) is essential for lymphoid organogenesis and controls apoptosis during thymopoiesis". Proceedings of the National Academy of Sciences of the United States of America. 97 (18): 10132–10137. Bibcode:2000PNAS...9710132K. doi:10.1073/pnas.97.18.10132. PMC 27750. PMID 10963675.
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  35. ^ Clinical trial number NCT02929862 for "Study of LYC-55716 in Adult Subjects With Locally Advanced or Metastatic Cancer" at ClinicalTrials.gov
  36. ^ "Lycera Announces Initiation of Phase 1b Study of Novel Immuno-Oncology Candidate LYC-55716 in Combination with Pembrolizumab". January 2018.
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