Structure/function analysis of Na+-K+-ATPase central isoform-specific region: Involvement in PKC regulation

Sandrine V. Pierre, Marie Josée Duran, Deborah L. Carr, Thomas A. Pressley

Research output: Contribution to journalArticle

17 Scopus citations

Abstract

Specific functions served by the various Na+-K+-ATPase α-isoforms are likely to originate in regions of structural divergence within their primary structures. The isoforms are nearly identical, with the exception of the NH2 terminus and a 10-residue region near the center of each molecule (isoform-specific region; ISR). Although the NH2 terminus has been clearly identified as a source of isoform functional diversity, other regions seem to be involved. We investigated whether the central ISR could also contribute to isoform variability. We constructed chimeric molecules in which the central ISRs of rat α1- and α2-isoforms were exchanged. After stable transfection into opossum kidney cells, the chimeras were characterized for two properties known to differ dramatically among the isoforms: their K+ deocclusion pattern and their response to PKC activation. Comparisons with rat full-length α1- and α2-isoforms expressed under the same conditions suggest an involvement of the central ISR in the response to PKC but not in K+ deocclusion.

Original languageEnglish
Pages (from-to)F1066-F1074
JournalAmerican Journal of Physiology - Renal Physiology
Volume283
Issue number5 52-5
DOIs
StatePublished - Nov 2002

Keywords

  • Chimeras
  • Potassium deocclusion
  • Rat
  • α- and α-isoforms
  • α-subunit

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