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Prince Henrys Institute of Medical Research, Clayton, Victoria 3168, Australia
Address all correspondence and requests for reprints to: Dr. Peter J. Fuller, Prince Henrys Institute of Medical Research, P.O. Box 5152, Clayton, Victoria 3168, Australia. E-mail: peter.fuller{at}med.monash.edu.au
The molecular mechanisms by which corticosteroids affect fluid and
electrolyte balance are unclear. Though glucocorticoid-responsive genes
have been identified, genes regulated by aldosterone have not. CHIF
(channel-inducing factor gene) is a recently identified gene that is
up-regulated in the distal colon by chronic corticosteroid exposure, is
expressed in the kidney, and induces a K+-specific current
in Xenopus oocytes. The predicted protein shows
similarity to
Na.K-ATPase, phospholemman, and Mat-8; all seem to
be involved in ion transport. CHIF thus presents as a potential
aldosterone target gene. In this study, CHIF expression was examined in
rats in the acute timeframe of 0.54 h after corticosteroid
administration. CHIF messenger RNA showed up-regulation by both
mineralocorticoid and glucocorticoid receptor agonists in the distal
colon, which was not diminished by cycloheximide. Corticosteroid
regulation was not observed in the kidney. Basal and induced expression
was absent in the lung and in all gastrointestinal tissues except
colon, with expression increasing proximal to distal. CHIF is the first
gene to show acute regulation by aldosterone and thus encodes a
candidate aldosterone-induced protein. In addition,
Na.K-ATPase gene
expression was found to be very low in colon and significantly higher
in kidney. Regulation by corticosteroids was not evident in either
tissue.
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