Key result
Kcnq1, Kcnh2, and Kcne3 are widely distributed and coexpressed in various organs during mouse embryogenesis, supporting the need for balanced alpha- and beta-subunit expression.
Emphasizes developmental K+ channel balance in mice; leaves open human arrhythmia or therapeutic relevance.
Voltage-dependent potassium channels consist of a pore-forming alpha-subunit, which is modulated by additional beta-ancillary or regulatory subunits. Kcnq1 and Kcnh2 alpha-channel subunits play pivotal roles in the developing and adult heart. However, Kcnq1 and Kcnh2 have a much wider expression profile than strictly confined to the myocardium, similar to their putative regulatory Kcne1-5 beta-subunits. At present, the distribution of distinct potassium channel subunits has been partially mapped in adult tissues, whereas almost no information is available during embryonic development. In this study, we report a detailed analysis of Kcnq1, Kcnh2, and Kcne3 protein expression during mouse embryogenesis. Our results demonstrate that Kcnq1 and Kcnh2 are widely distributed. Coexpression of both alpha-subunits is observed in a wide variety of organs, such as heart and the skeletal muscle, whereas others display unique Kcnq1 or Knch2 expression. Interestingly, Kcne3 expression is also widely observed in distinct tissue layers during embryogenesis, supporting the notion that an exquisite balance of alpha- and beta-subunit expression is required for modulating potassium conductance in distinct organs and tissue layers.
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Castro et al. (2006) studied Mouse embryonic development. Protein distribution analysis of Kcnq1, Kcnh2, and Kcne3 was evaluated on Protein expression distribution during mouse embryogenesis. Kcnq1, Kcnh2, and Kcne3 are widely distributed and coexpressed in various organs during mouse embryogenesis, supporting the need for balanced alpha- and beta-subunit expression.
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