JmjC domain-containing histone demethylation protein 2C; Jumonji domain-containing protein 1C; thyroid receptor-interacting protein 8; TR-interacting protein 8; TRIP-8 (JMJD1C, JHDM2C, KIAA1380, TRIP8)
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Function
- probable histone demethylase that specifically demethylates Lys-9 of histone H3, thus playing a role in histone code
- demethylation of Lys generates formaldehyde & succinate
- may be involved in hormone-dependent transcriptional activation, by participating in recruitment to androgen-receptor target genes (putative)
- phosphorylated upon DNA damage, probably by ATM or ATR
- interacts specifically with the ligand-binding domain of the thyroid hormone receptor; requires presence of thyroid hormone for its interaction
Structure
- Leu-Xaa-Xaa-Leu-Leu (LXXLL) motifs are known to mediate association with nuclear receptors (putative)
- belongs to the JHDM2 histone demethylase family
- contains 1 JmjC domain
Compartment
Alternative splicing
named isoforms=2
Pathology
- JMJD1C gene variants associated positively endogenous serum testosterone[3] & with thromboembolism (odds ratio, 2.1) & heart failure (OR, 7.8) in men[2]
- associateions not as marked in women
More general terms
- thyroid hormone receptor interacting protein (TRIP)
- zinc finger protein
- phosphoprotein
- histone demethylase
References
- ↑ UniProt http://www.uniprot.org/uniprot/Q15652.html
- ↑ 2.0 2.1 Luo S et al. Association of genetically predicted testosterone with thromboembolism, heart failure, and myocardial infarction: Mendelian randomisation study in UK Biobank. BMJ 2019 Mar 6; 364:l476 PMID: https://www.ncbi.nlm.nih.gov/pubmed/30842065 Free PMC Article https://www.bmj.com/content/364/bmj.l476
- ↑ 3.0 3.1 Jin G, Sun J, Kim ST, Feng J et al Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men. Hum Mol Genet. 2012 Dec 1;21(23):5222-8. Epub 2012 Aug 30. PMID: https://www.ncbi.nlm.nih.gov/pubmed/22936694 Free PMC Article