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A novel mutant allele of Ncx1: a single amino acid substitution leads to cardiac dysfunction

Wansleeben, C. and Feitsma, H. and Tertoolen, L.G.J. and Kroon, C. and Guryev, V. and Cuppen, E. and Meijlink, F.C.P.W. (2010) A novel mutant allele of Ncx1: a single amino acid substitution leads to cardiac dysfunction. International journal of developmental biology, 54, 1465-71. ISSN 0214-6282.

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Official URL: http://dx.doi.org/10.1387/ijdb.093051cw

Abstract

The biological role and structure-function relationship of the Na(+)Ca(2+) exchanger NCX1 have been the subject of much investigation. Subtle mutagenesis to study the function of a protein seems only feasible in in vitro systems, but genetic forward screens have the potential to provide in vivo models to study single amino acid substitutions. In a genetic screen in mouse, we have isolated a mutant line carrying a novel mutant allele of the mouse Ncx1 gene. In this allele, a point mutation causes the substitution of a highly conserved asparagine residue (N874) with lysine. Accepted models for NCX1 structure propose that the affected amino acid is located in one of the reentrant membrane loops and experiments in vitro have identified N874 as critical for the ion transport function of NCX1. We found severe circulation defects and defective placentation in homozygous Ncx1(N87K4) mutant embryos, making the phenotype essentially indistinguishable from those of previously described null mutants. By ex vivo analysis, we demonstrated intrinsic functional abnormalities of cardiomyocytes. Western blot analysis and immunohistochemistry demonstrated normal levels and subcellular localization of the altered protein, ruling out the possibility that the abnormalities are a mere consequence of a major disturbance of protein structure. This study confirms and extends studies in vitro indicating the significance of amino acid N874 for the function of the NCX1 protein. It provides an in vivo model for this mutation and demonstrates the potential of forward genetic screens in a mammalian system.

Item Type:Article
Institutes:Hubrecht Instituut
ID Code:9524
Deposited On:11 Feb 2011 01:00
Last Modified:07 Sep 2011 17:01

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