Partitioning of Tissue Expression Accompanies Multiple Duplications of the Na+/K+ ATPase α Subunit Gene

  1. Fabrizio C. Serluca1,
  2. Arend Sidow2,
  3. John D. Mably1, and
  4. Mark C. Fishman1,3
  1. 1Cardiovascular Research Center and Developmental Biology Laboratory, Massachusetts General Hospital, and Department of Medicine, Harvard Medical School, Boston, Massachusetts 02119, USA; 2Departments of Pathology and Genetics, Stanford University, Stanford, California 94305, USA

Abstract

Vertebrate genomes contain multiple copies of related genes that arose through gene duplication. In the past it has been proposed that these duplicated genes were retained because of acquisition of novel beneficial functions. A more recent model, the duplication-degeneration-complementation hypothesis (DDC), posits that the functions of a single gene may become separately allocated among the duplicated genes, rendering both duplicates essential. Thus far, empirical evidence for this model has been limited to theengrailed and sox family of developmental regulators, and it has been unclear whether it may also apply to ubiquitously expressed genes with essential functions for cell survival. Here we describe the cloning of three zebrafish α subunits of the Na(+),K(+)-ATPase and a comprehensive evolutionary analysis of this gene family. The predicted amino acid sequences are extremely well conserved among vertebrates. The evolutionary relationships and the map positions of these genes and of other α-like sequences indicate that both tandem and ploidy duplications contributed to the expansion of this gene family in the teleost lineage. The duplications are accompanied by acquisition of clear functional specialization, consistent with the DDC model of genome evolution.

[The sequence data described in this paper have been submitted to the GenBank data library under accession nos. AY028628, AY028629, and AY028630]

Footnotes

  • 3 Corresponding author.

  • E-MAIL fishman{at}cvrc.mgh.harvard.edu; FAX (617) 726-5806.

  • Article published on-line before print: Genome Res., 10.1101/gr.192001.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.192001.

    • Received April 12, 2001.
    • Accepted June 4, 2001.
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