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AJP - Cell Physiology, Vol 255, Issue 1 C12-C18, Copyright © 1988 by American Physiological Society
ARTICLES |
M. Mitas, C. Coogan and J. J. Gargus
Department of Physiology, Emory University School of Medicine, Atlanta, Georgia 30322.
We have successfully transfected mouse genomic DNA containing a mutant putative K+ channel gene into murine LMTK- cells. Incorporation of the mutant gene allowed primary transformants to express the mutant cell phenotype of growth at a subthreshold K+ concentration and, furthermore, caused these primary transformants to display the same characteristics of growth and unidirectional K+ flux as the mutant cell line, LTK-1, from which the genomic DNA was derived. A cosmid genomic library was formed from LTK-1 mutant DNA and shown by transfection experiments to contain at least one unique cosmid clone containing a functional copy of the mutant putative K+ channel gene.
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