Expanded Functional Diversity of Shaker K.sup.+ Channels in Cnidarians Is Driven by Gene Expansion

• Published in: PloS one Vol. 7; no. 12; p. e51366
• Main Authors: Jegla, Timothy, Marlow, Heather Q, Chen, Bihan, Simmons, David K, Jacobo, Sarah M, Martindale, Mark Q
• Format: Journal Article
• Language: English
• Published: Public Library of Science 10.12.2012
• Subjects: Cladistic analysis; Genes; Genomes; Genomics; Phylogeny
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0051366

The genome of the cnidarian Nematostella vectensis (starlet sea anemone) provides a molecular genetic view into the first nervous systems, which appeared in a late common ancestor of cnidarians and bilaterians. Nematostella has a surprisingly large and diverse set of neuronal signaling genes including paralogs of most neuronal signaling molecules found in higher metazoans. Several ion channel gene families are highly expanded in the sea anemone, including three subfamilies of the Shaker K.sup.+ channel gene family: Shaker (Kv1), Shaw (Kv3) and Shal (Kv4). In order to better understand the physiological significance of these voltage-gated K.sup.+ channel expansions, we analyzed the function of 18 members of the 20 gene Shaker subfamily in Nematostella. Six of the Nematostella Shaker genes express functional homotetrameric K.sup.+ channels in vitro. These include functional orthologs of bilaterian Shakers and channels with an unusually high threshold for voltage activation. We identified 11 Nematostella Shaker genes with a distinct "silent" or "regulatory" phenotype; these encode subunits that function only in heteromeric channels and serve to further diversify Nematostella Shaker channel gating properties. Subunits with the regulatory phenotype have not previously been found in the Shaker subfamily, but have evolved independently in the Shab (Kv2) family in vertebrates and the Shal family in a cnidarian. Phylogenetic analysis indicates that regulatory subunits were present in ancestral cnidarians, but have continued to diversity at a high rate after the split between anthozoans and hydrozoans. Comparison of Shaker family gene complements from diverse metazoan species reveals frequent, large scale duplication has produced highly unique sets of Shaker channels in the major metazoan lineages.