A divergent CFTR homologue:: highly regulated salt transport in the euryhaline teleost F-heteroclitus

被引:129
作者
Singer, TD
Tucker, SJ
Marshall, WS
Higgins, CF
机构
[1] Univ Oxford, John Radcliffe Hosp, Inst Mol Med, Nuffield Dept Clin Biochem, Oxford OX3 9DS, England
[2] Univ Oxford, John Radcliffe Hosp, Inst Mol Med, Imperial Canc Res Fund Labs, Oxford OX3 9DS, England
[3] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
[4] St Francis Xavier Univ, Dept Biol, Antigonish, NS B2G 2W5, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1998年 / 274卷 / 03期
关键词
cystic fibrosis transmembrane conductance regulator; chloride channel; killifish; gill; Xenopus expression; osmoregulation; cystic fibrosis; Fundulus heteroclitus;
D O I
10.1152/ajpcell.1998.274.3.C715
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The killifish, Fundulus heteroclitus, is a euryhaline teleost fish capable of adapting rapidly to transfer from freshwater (FW) to four times seawater (SW). To investigate osmoregulation at a molecular level, a 5.7-kilobase cDNA homologous to human cystic fibrosis transmembrane conductance regulator (hCFTR) was isolated from a gill cDNA library from SW-adapted killifish. This cDNA encodes a protein product (kfCFTR) that is 59% identical to hCFTR, the most divergent form of CFTR characterized to date. Expression of kfCFTR in Xenopus oocytes generated adenosine 3',5'-cyclic monophosphate-activated, Cl--selective currents similar to those generated by hCFTR. In SW-adapted killifish, kfCFTR was expressed at high levels in the gill, opercular epithelium, and intestine. After abrupt exposure of FW-adapted killifish to SW, kfCFTR expression in the gill increased severalfold, suggesting a role for kfCFTR in salinity adaptation. Under similar conditions, plasma Na+ levels rose significantly after 8 h and then fell, although it is not known whether these changes are directly responsible for the changes in hfCFTR expression. The killifish provides a unique opportunity to understand teleost osmoregulation and the role of CFTR.
引用
收藏
页码:C715 / C723
页数:9
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