The wealth of accumulating data from the Caenorhabditis elegans genome
sequencing project has rapidly accelerated the discovery of novel pot
assium channel genes and now places within reach the possibility of de
scribing the total complement of potassium channels used by an individ
ual species. Using annotated GenBank sequences, BLAST searches of unfi
nished sequences and degenerate oligonucleotide polymerase chain react
ion (PCR) screens, we have identified and compiled genes for 38 C. ele
gans potassium channel and two cyclic nucleotide-gated cation channel
subunits, representing eight conserved multigene families. Novel famil
ies of potassium channel genes were revealed, as well as conserved hom
ologues of all known vertebrate families. Two separate families repres
ent C. elegans homologues for human potassium channels recently implic
ated in hereditary long QT arrhythmias. Of particular note is an excep
tionally large class of at least 23 genes with a novel subunit structu
re having two tandem 'P' domains; these channels may form as dimers in
contrast to all other potassium channel types which form as tetramers
. The 40 potassium channel genes are evenly distributed on all six C.
elegans chromosomes, with the exception of three instances of gene clu
stering on the fifth and X chromosomes. Copyright (C) 1996 Elsevier Sc
ience Ltd