Differential evolution of voltage-gated sodium channels in tetrapods and teleost fishes

• Published in: Molecular biology and evolution Vol. 28; no. 1; pp. 859 - 871
• Main Authors: Widmark, Jenny, Sundström, Görel, Ocampo Daza, Daniel, Larhammar, Dan
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.01.2011
• Subjects: activin receptor; Amino Acid Sequence; Amino acids; Amniota; Animals; AT-AC intron; Base Sequence; Biological Evolution; Chromosomes; Comparative analysis; CSRNP (cysteine-serine-rich nuclear protein); Evolution, Molecular; Fish; Fishes - genetics; Genes; HOX; Humans; Mammals; MEDICIN; MEDICINE; Models, Molecular; Molecular Sequence Data; Multigene Family; Phylogenetics; Phylogeny; Pisces; Protein Conformation; Protein Isoforms - chemistry; Protein Isoforms - genetics; Protein Subunits - chemistry; Protein Subunits - genetics; Proteins; Sequence Alignment; Sodium; Sodium Channels - chemistry; Sodium Channels - classification; Sodium Channels - genetics; Teleostei; TGF-beta receptor; Vertebrates; Voltage-gated sodium channel
• ISSN: 0737-4038; 1537-1719; 1537-1719
• DOI: 10.1093/molbev/msq257

The voltage-gated sodium channel (SCN) alpha subunits are large proteins with central roles in the generation of action potentials. They consist of approximately 2,000 amino acids encoded by 24-27 exons. Previous evolutionary studies have been unable to reconcile the proposed gene duplication schemes with the species distribution and molecular phylogeny of the genes. We have carefully annotated the complete SCN gene sequences, correcting numerous database errors, for a broad range of vertebrate species and analyzed their phylogenetic relationships. We have also compared the chromosomal positions of the SCN genes relative to adjacent gene families. Our studies show that the ancestor of the vertebrates probably had a single sodium channel gene with two characteristic AT-AC introns, the second of which is unique to vertebrate SCN genes. This ancestral gene, located close to a HOX gene cluster, was quadrupled along with HOX in the two rounds of basal vertebrate tetraploidizations to generate the ancestors of the four channels SCN1A, SCN4A, SCN5A, and SCN8A. The third tetraploidization in the teleost fish ancestor doubled this set of genes and all eight are still present in at least three of four investigated teleost fish genomes. In tetrapods, the gene family expanded by local duplications before the radiation of amniotes, generating the cluster SCN5A, SCN10A, and SCN11A on one chromosome and the cluster SCN1A, SCN2A, SCN3A, and SCN9A on a different chromosome. In eutherian mammals, a tenth gene, SCN7A, arose in a local duplication in the SCN1A gene cluster. The SCN7A gene has undergone rapid evolution and has lost the ability to cause action potentials-instead, it functions as a sodium sensor. The three genes in the SCN5A cluster were translocated from the HOX-bearing chromosome in a mammalian ancestor along with several adjacent genes. This evolutionary scenario is supported by the adjacent TGF-β receptor superfamily (comprised of five distinct families) and the cysteine-serine-rich nuclear protein gene family as well as the HOX clusters. The independent expansions of the SCN repertoires in tetrapods and teleosts suggest that the functional diversification may differ between the two lineages.