Cloning of the Drosophila Shaker gene established that a neurological
phenotype including locomotor dysfunction can be caused by a mutation
in a voltage-gated potassium (K) channel gene. Shaker sequences have b
een used to isolate a large family of related K channel genes from bot
h flies and mammals. Toward elucidating the evolutionary relationship
between loci and the potential causal connection that K channels may h
ave to mammalian genetic disorders, we report here the genetic mapping
of 12-16 different murine, voltage-gated K channel genes. We find tha
t multiple genes, in some cases from distantly related K channel subfa
milies, occur in clusters in the mouse genome. These mapping results s
uggest that the K channel gene subfamilies arose through ancient local
ized gene duplication events, followed by chromosomal duplications and
rearrangements as well as further gene duplication. We also note that
several neurologic disorders of both mouse and human are associated w
ith the chromosomal regions containing K channel genes. (C) 1994 Acade
mic Press, Inc.