Here, we report the presence of two splice variants of the human epithelial
sodium channel alpha subunit (h alpha ENaC) containing Alu cassette, namel
y h alpha ENaC+22 and h alpha ENaC+Alu, in various tissues. Functional expr
ession of these splice variants with hENaC beta and gamma subunits produced
loss-of-channel activity in the Xenopus oocyte expression system. Interest
ingly, coexpression of h alpha ENaC+22 or h alpha ENaC+Alu, respectively, w
ith wild type hENaC alpha, beta, and gamma subunits enhanced the expression
of amiloride-sensitive current in oocytes. The presence of Alu sequences i
n the 3 ' -untranslated region of h gamma ENaC was also identified. (C) 200
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