Four related genes, Shaker, Shab, Shaw, and Shal, encode voltage-gated
K+ channels in Drosophila. Multigene subfamilies corresponding to eac
h of these Drosophila genes have been identified in rodents and primat
es; this suggests that the four genes are older than the common ancest
or of present-day insects and mammals and that the expansion of each i
nto a family occurred before the divergence of rodents and primates. I
n order to define these evolutionary relationships more precisely and
to facilitate the search for mammalian candidate K+ channel gene mutat
ions, we have mapped members of the Shaw-homologous gene family in hum
ans and mice. Fluorescence in situ hybridization analysis of human met
aphase chromosomes mapped KCNC2 (KShIIIA, KV3.2) and KCNC3 (KShIIID, K
V3.3) to Chromosome (Chr) 19q13.3-q13.4. Inheritance patterns of DNA r
estriction fragment length variants in recombinant inbred strains of m
ice placed the homologous mouse genes on distal Chr 10 near Ms15-8 and
Mdm-1. The mouse Kcnc1 (KShIIIB, NGK2-KV4, KV3.1) gene mapped to Chr
7 near Tam-1. These results are consistent with the hypothesis that th
e generation of the mammalian KCNC gene family included both duplicati
on events to generate family members in tandem arrays (KCNC2, KCNC3) a
nd dispersion of family members to unlinked chromosomal sites (KCNC1).
The KNCN2 and KCNC3 genes define a new synteny group between humans a
nd mice