DefinitionThis section has been translated automatically.
The RORC gene (RFORC stands for "RAR Related Orphan Receptor C") is a protein coding gene located on chromosome 1q21. Two transcript variants encoding different isoforms have been found for this gene.
The RORC protein encoded by the RORC gene is a DNA-binding transcription factor, belongs to the NR1 subfamily of nuclear hormone receptors, and is the major transcription factor responsible for the differentiation of T helper 17 cells.
Furthermore, the RORC gene plays a role in lymphoid organogenesis, thymopoiesis, and lymph node organogenesis (Michelini S et al. 2021). In addition, the RORC protein is thought to inhibit the expression of Fas ligand as well as IL-2. Signaling pathways utilized include cytokine signaling in the immune system and cytokine production by Th17 cells in cystic fibrosis.
Clinical pictureThis section has been translated automatically.
Diseases associated with RORC include:
Autosomal recessive immunodeficiency 42 (IMD42; see also Mendelian susceptibility to mycobacterial diseases), a rare immunodeficiency syndrome caused by a mutation in the RORC gene.
and
secondary progressive multiple sclerosis.
Mutations in RORC may predispose to lymphedema (Michelini S et al.2021).
LiteratureThis section has been translated automatically.
- Ivanov II et al (2006) The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells. Cell 126:1121-1133
- Kurebayashi S et al (2000) Retinoid-related orphan receptor gamma (ROR-gamma) is essential for lymphoid organogenesis and controls apoptosis during thymopoiesis. Proc Nat Acad Sc. 97: 10132-10137.
- Leija-Martínez JJ et al. (2020) Decreased methylation profiles in the TNFA gene promoters in type 1 macrophages and in the IL17A and RORC gene promoters in Th17 lymphocytes have a causal association with non-atopic asthma caused by obesity: A hypothesis" Med. Hypotheses 2020 144:110181.
- Michelini S et al (2021) Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants. Lymphat Res Biol 19:129-133.
- Okada S et al (2015) Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations. Science 349: 606-613.