Persistence of the ABCC6 genes and the emergence of the bony skeleton in vertebrates

• Published in: Scientific reports 2018-04, Vol.8 (1), p.6027-13, Article 6027
• Main Authors: Parreira, Bruna, Cardoso, João C. R., Costa, Rita, Couto, Ana Rita, Bruges-Armas, Jácome, Power, Deborah M.
• Format: Article
• Language: English
• Subjects: 38/39; 38/77; 45/90; 631/181/757; 631/208/199; Amino acids; Calcification; Calcification (ectopic); Comparative analysis; Endoskeleton; Gene expression; Genomes; Humanities and Social Sciences; Invertebrates; Mineralization; multidisciplinary; Mutation; Protein transport; Scales; Science; Science (multidisciplinary); Skin; Vertebrates
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-24370-7

The ATP-binding cassette transporter 6 ( ABCC6 ) gene encodes a cellular transmembrane protein transporter (MRP6) that is involved in the regulation of tissue calcification in mammals. Mutations in ABCC6 are associated with human ectopic calcification disorders. To gain insight into its evolution and involvement in tissue calcification we conducted a comparative analysis of the ABCC6 gene and the related gene ABCC1 from invertebrates to vertebrates where a bony endoskeleton first evolved. Taking into consideration the role of ABCC6 in ectopic calcification of human skin we analysed the involvement of both genes in the regeneration of scales, mineralized structures that develop in fish skin. The ABCC6 gene was only found in bony vertebrate genomes and was absent from Elasmobranchs, Agnatha and from invertebrates. In teleost fish the abcc6 gene duplicated but the two genes persisted only in some teleost genomes. Six disease causing amino acid mutations in human MRP6 are a normal feature of abcc6 in fish, suggesting they do not have a deleterious effect on the protein. After scale removal the abcc6 (5 and 10 days) and abcc1 (10 days) gene expression was up-regulated relative to the intact control skin and this coincided with a time of intense scale mineralization.