Dataset Information

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

ABSTRACT: There are four isoforms of the alpha subunit (alpha1-4) and three isoforms of the beta subunit (beta1-3) of Na,K-ATPase, with distinct tissue-specific distribution and physiological functions. alpha2 is thought to play a key role in cardiac and smooth muscle contraction and be an important target of cardiac glycosides. An alpha2-selective cardiac glycoside could provide important insights into physiological and pharmacological properties of alpha2. The isoform selectivity of a large number of cardiac glycosides has been assessed utilizing alpha1beta1, alpha2beta1, and alpha3beta1 isoforms of human Na,K-ATPase expressed in Pichia pastoris and the purified detergent-soluble isoform proteins. Binding affinities of the digitalis glycosides, digoxin, beta-methyl digoxin, and digitoxin show moderate but highly significant selectivity (up to 4-fold) for alpha2/alpha3 over alpha1 (K(D) alpha1 > alpha2 = alpha3). By contrast, ouabain shows moderate selectivity ( approximately 2.5-fold) for alpha1 over alpha2 (K(D) alpha1

SUBMITTER: Katz A

PROVIDER: S-EPMC2885237 | biostudies-literature | 2010 Jun

REPOSITORIES: biostudies-literature

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Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

Katz Adriana A Lifshitz Yael Y Bab-Dinitz Elizabeta E Kapri-Pardes Einat E Goldshleger Rivka R Tal Daniel M DM Karlish Steven J D SJ

The Journal of biological chemistry 20100413 25

There are four isoforms of the alpha subunit (alpha1-4) and three isoforms of the beta subunit (beta1-3) of Na,K-ATPase, with distinct tissue-specific distribution and physiological functions. alpha2 is thought to play a key role in cardiac and smooth muscle contraction and be an important target of cardiac glycosides. An alpha2-selective cardiac glycoside could provide important insights into physiological and pharmacological properties of alpha2. The isoform selectivity of a large number of ca ...[more]

PMID: 20388710

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Project description:BACKGROUND AND METHODS:Multiple Na+/K+-ATPase (NKA) ?-subunit isoforms express differentially in response to salinity transfer in teleosts but we observed that the isoform nomenclature is inconsistent with the phylogenetic relationship of NKA ?-genes. We cloned the catalytic NKA ?-subunit isoforms in eels and medaka, analyzed the time course of their expressions in osmoregulatory tissues after transfer from freshwater (FW) to seawater (SW), and performed phylogenetic analyses to deduce an evolutionary scenario that illustrates how various duplication events have led to the current genomic arrangement of NKA ?-genes in teleosts. RESULTS AND DISCUSSION:Five and six ?-subunits were cloned in eels and medaka respectively. In eels, the commonly-reported ?1a and ?1b isoforms were absent while the ?1c isoform was diversified instead (?1c-1, ?1c-2, ?1c-3, ?2, and ?3 in eels). Phylogenetic estimation indicated that the ?1a and ?1b isoforms from salmon, tilapia, and medaka were generated by independent duplication events and thus they are paralogous isoforms. Re-examination of expression changes of known isoforms after salinity challenge revealed that the isoforms selected as predominant SW-types varied among teleost lineages. Diversification of ?1 isoforms occurred by various types of gene duplication, or by alternative transcription among tandem genes to form chimeric transcripts, but there is no trend for more ?1 copies in euryhaline species. Our data suggest that the isoform switching between FW (?1a predominates) and SW (?1b predominates) that occurs in salmonids is not universal in teleosts. Instead, in eels, ?1c-1 was the major ?-subunit upregulated gill, intestine, and kidney in SW. Localization of both NKA mRNA and protein showed consistent upregulation in gill and intestine in SW eels, but not in renal distal and collecting tubules, where low transcript expression levels were accompanied by high protein levels, suggesting a tissue-specific translational regulation that determines and fine-tunes the NKA expression. In medaka, ?1b was upregulated in SW in anterior intestine while most other ?-subunit isoforms were less responsive to salinity changes. CONCLUSION:By integrating gene expression and phylogenetic results, we propose that the major NKA ?-subunits for SW acclimation were not ancestrally selected, but rather were flexibly determined in lineage-specific fashion in teleosts.

Dataset Information

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

Publications

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

Similar Datasets

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