TY - JOUR
T1 - A corticosteroid-induced gene expressing an "IsK-like" K+ channel activity in Xenopus oocytes
AU - Attali, Bernard
AU - Latter, Hedva
AU - Rachamim, Nurit
AU - Garty, Haim
PY - 1995/6/20
Y1 - 1995/6/20
N2 - Screening a rat colon cDNA library for aldosterone-induced genes resulted in the molecular cloning of a cDNA whose corresponding mRNA is strongly induced in the colon by dexamethasone, aldosterone, and a low NaCl diet. A similar mRNA was detected in kidney papilla but not in brain, heart, or skeletal muscle. Xenopus laevis oocytes injected with cRNA synthesized from this clone, designated CHIF (channel-inducing factor), express a K+-specific channel activity. The biophysical, pharmacological, and regulatory characteristics of this channel are very similar to those reported before for IsK (minK). These include: slow (τ > 20 s) activation by membrane depolarization with a threshold potential above -50 mV, blockade by clofilium, inhibition by phorbol ester, and activation by 8-bromoadenosine 3′,5′-cyclic monophosphate and high cytoplasmic Ca2+. The primary structure of this clone, however, shows no homology to IsK. Instead, CHIF exhibits >50% similarity to two other short bitopic membrane proteins, phospholemman and the γ subunit of Na+,K+-ATPase. The data are consistent with the possibility that CHIF is a member of a family of transmembrane regulators capable of activating endogenous oocyte transport proteins.
AB - Screening a rat colon cDNA library for aldosterone-induced genes resulted in the molecular cloning of a cDNA whose corresponding mRNA is strongly induced in the colon by dexamethasone, aldosterone, and a low NaCl diet. A similar mRNA was detected in kidney papilla but not in brain, heart, or skeletal muscle. Xenopus laevis oocytes injected with cRNA synthesized from this clone, designated CHIF (channel-inducing factor), express a K+-specific channel activity. The biophysical, pharmacological, and regulatory characteristics of this channel are very similar to those reported before for IsK (minK). These include: slow (τ > 20 s) activation by membrane depolarization with a threshold potential above -50 mV, blockade by clofilium, inhibition by phorbol ester, and activation by 8-bromoadenosine 3′,5′-cyclic monophosphate and high cytoplasmic Ca2+. The primary structure of this clone, however, shows no homology to IsK. Instead, CHIF exhibits >50% similarity to two other short bitopic membrane proteins, phospholemman and the γ subunit of Na+,K+-ATPase. The data are consistent with the possibility that CHIF is a member of a family of transmembrane regulators capable of activating endogenous oocyte transport proteins.
KW - Aldosterone
KW - Epithelial transport
KW - Ion channels
KW - Na,K-ATPase
KW - Phospholemman
UR - http://www.scopus.com/inward/record.url?scp=0029020393&partnerID=8YFLogxK
U2 - 10.1073/pnas.92.13.6092
DO - 10.1073/pnas.92.13.6092
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C2 - 7597086
AN - SCOPUS:0029020393
SN - 0027-8424
VL - 92
SP - 6092
EP - 6096
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 13
ER -