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J Physiol Volume 548, Number 3, 815-822, May 1, 2003 DOI: 10.1113/jphysiol.2002.033704
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J Physiol (2003), 548.3, pp. 815-822
© Copyright 2003 D 2003 The Physiological Society
DOI: 10.1113/jphysiol.2002.033704

Concordant expression of KChIP2 mRNA, protein and transient outward current throughout the canine ventricle

Barbara Rosati, Frederic Grau *, Samantha Rodriguez, Huilin Li †, Jeanne M. Nerbonne † and David McKinnon *

Department of Physiology and Biophysics and * Department of Neurobiology and Behavior, Institute of Molecular Cardiology, State University of New York at Stony Brook, Stony Brook, NY 11794 and †Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St Louis, MO 63110, USA

Expression of the transient outward K+ current (Ito) was analysed in nine different regions of the canine ventricle. In addition to the previously described transmural gradients in the right and left ventricular free walls, an inverted U-shaped pattern of Ito expression was observed in the interventricular septum. The mRNA and protein expression for the K+ channel beta subunit KChIP2 were examined in the same tissues. The KChIP2 protein levels closely matched mRNA expression in all regions of the ventricle and paralleled the density of Ito. The global pattern of gene expression in human epicardial and endocardial tissue was examined using microarrays. Only 0.1 % of the genes expressed in the human ventricle displayed the same expression pattern as the KChIP2 gene in left ventricle. It is unlikely, therefore, that the reported distribution of KChIP2 protein within the ventricle can be explained by a cross-reaction of the anti-KChIP2 antibody with a different protein. It is concluded that transcriptional regulation of the KChIP2 gene is a primary determinant of Ito expression in heart.



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