The Repertoire of Na,K-ATPase α and β Subunit Genes Expressed in the Zebrafish, Danio rerio

  1. S. Johannes R. Rajarao1,
  2. Victor A. Canfield1,
  3. Manzoor-Ali P.K. Mohideen2,
  4. Yi-Lin Yan3,
  5. John H. Postlethwait3,
  6. Keith C. Cheng2, and
  7. Robert Levenson1,4
  1. 1Department of Pharmacology and 2The Jake Gittlen Cancer Research Institute and Department of Pathology, Pennsylvania State College of Medicine, Hershey, Pennsylvania 17033, USA; 3Institute of Neuroscience, University of Oregon, Eugene, Oregon 97403, USA

Abstract

We have identified a cohort of zebrafish expressed sequence tags encoding eight Na,K-ATPase α subunits and five β subunits. Sequence comparisons and phylogenetic analysis indicate that five of the zebrafish α subunit genes comprise an α1-like gene subfamily and two are orthologs of the mammalian α3 subunit gene. The remaining α subunit clone is most similar to the mammalian α2 subunit. Among the five β subunit genes, two are orthologs of the mammalian β1 isoform, one represents a β2 ortholog, and two are orthologous to the mammalian β3 subunit. Using zebrafish radiation hybrid and meiotic mapping panels, we determined linkage assignments for each α and β subunit gene. Na,K-ATPase genes are dispersed in the zebrafish genome with the exception of four of the α1-like genes, which are tightly clustered on linkage group 1. Comparative mapping studies indicate that most of the zebrafish Na,K-ATPase genes localize to regions of conserved synteny between zebrafish and humans. The expression patterns of Na,K-ATPase α and β subunit genes in zebrafish are quite distinctive. No two α or β subunit genes exhibit the same expression profile. Together, our data imply a very high degree of Na,K-ATPase isoenzyme heterogeneity in zebrafish, with the potential for 40 structurally distinct α/β subunit combinations. Differences in expression patterns of α and β subunits suggest that many of the isoenzymes are also likely to exhibit differences in functional properties within specific cell and tissue types. Our studies form a framework for analyzing structure function relationships for sodium pump isoforms using reverse genetic approaches.

Footnotes

  • 4 Corresponding author.

  • E-MAIL rlevenson{at}hmc.psu.edu; FAX (717) 531-5013.

  • Article and publication are at www.genome.org/cgi/doi/10.1101/gr.186001.

    • Received February 21, 2001.
    • Accepted April 16, 2001.
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