In plants a large diversity of inwardly rectifying K+ channels (K-in c
hannels) has been observed between tissues and species. However, only
three different types of voltage-dependent plant K+ uptake channel sub
families have been cloned so tar. they relate either to KAT1, AKT1, or
AtKC1. To explore the mechanisms underlying the channel diversity, we
investigated the assembly of plant inwardly rectifying alpha-subunits
. cRNA encoding five different K+ channel alpha-subunits of the three
subfamilies (KAT1, KST1, AKT1, SKT1, and AtKC1) which were isolated fr
om different tissues, species, and plant families (Arabidopsis thalian
a and Solanum tuberosum) was reciprocally co-injected into Xenopus ooc
ytes. We identified plant K+ channels as multimers. Moreover, using K channel mutants expressing different sensitivities to voltage, Cs+, C
a2+, and H+, we could prove heteromers on the basis of their altered v
oltage and modulator susceptibility. We discovered that, in contrast t
o animal K+ channel alpha-subunits, functional aggregates of plant K+,
channel alpha-subunits assembled indiscriminately. Interestingly, AKT
-type channels from A. thaliana and S. tuberosum, which as homomers we
re electrically silent in oocytes after co-expression, mediated K+ cur
rents. Our findings suggest that K+ channel diversity in plants result
s from nonselective heteromerization of different alpha-subunits, and
thus depends on the spatial segregation of individual alpha-subunit po
ols and the degree of temporal overlap and kinetics of expression.