Regulator of Calcineurin 1 (RCAN1)
Regulator of calcineurin 1 (RCAN1) was first isolated by Fuentes et al. in 1995 during a search for genes associated with clinical features of Down syndrome (e.g., mental retardation and congenital heart disease) (Fuentes et al. 1995). Coding sequences of RCAN1 were identified from the 21q22.1–q22.2 region of human chromosome 21 by an Alu-splice PCR method. It was initially thought that RCAN1 was significantly associated with the Down syndrome phenotype (Fuentes et al. 1997b), thus RCAN1 was first designated Down Syndrome Critical Region 1 (DSCR1). Future studies showed that the DSCR1 gene product is a calcineurin regulator, and the new name “regulator of calcineurin (RCAN)” was adopted to describe the gene function. Although RCAN1 is still referred to as DSCR1, ADAPT78, MCIP1, Calcipressin1, RCN-1,...
- Minami T, Horiuchi K, Miura M, Abid MR, Takabe W, Noguchi N, Kohro T, Ge X, Aburatani H, Hamakubo T, et al. Vascular endothelial growth factor- and thrombin-induced termination factor, Down syndrome critical region-1, attenuates endothelial cell proliferation and angiogenesis. J Biol Chem. 2004;279:50537–54.PubMedCrossRefGoogle Scholar
- Mulero MC, Aubareda A, Orzaez M, Messeguer J, Serrano-Candelas E, Martinez-Hoyer S, Messeguer A, Perez-Paya E, Perez-Riba M. Inhibiting the calcineurin-NFAT (nuclear factor of activated T cells) signaling pathway with a regulator of calcineurin-derived peptide without affecting general calcineurin phosphatase activity. J Biol Chem. 2009;284:9394–401.PubMedCrossRefGoogle Scholar