[HTML][HTML] Molecular and functional characterization of an amphibian urea transporter

C Couriaud, C Leroy, M Simon, C Silberstein… - … et Biophysica Acta (BBA …, 1999 - Elsevier
C Couriaud, C Leroy, M Simon, C Silberstein, P Bailly, P Ripoche, G Rousselet
Biochimica et Biophysica Acta (BBA)-Biomembranes, 1999Elsevier
We report the characterization of a frog (Rana esculenta) urea transporter (fUT). The cloned
cDNA is 1.4 kb long and contains a putative open reading frame of 1203 bp. In frog urinary
bladder, the gene is expressed as two mRNAs of 4.3 and 1.6 kb. The fUT protein is 63.1 and
56.3% identical to rat UT-A2 and UT-B1, respectively. The internal duplication of UT-A2 and
UT-B, as well as the double LP box urea transporter signature sequence were found in this
amphibian urea transporter. When expressed in Xenopus oocytes, fUT induced a 10-fold …
We report the characterization of a frog (Rana esculenta) urea transporter (fUT). The cloned cDNA is 1.4 kb long and contains a putative open reading frame of 1203 bp. In frog urinary bladder, the gene is expressed as two mRNAs of 4.3 and 1.6 kb. The fUT protein is 63.1 and 56.3% identical to rat UT-A2 and UT-B1, respectively. The internal duplication of UT-A2 and UT-B, as well as the double LP box urea transporter signature sequence were found in this amphibian urea transporter. When expressed in Xenopus oocytes, fUT induced a 10-fold increase in urea permeability, which was blocked by both phloretin and mercurial reagents. The fUT protein did not transport thiourea, but the fUT-mediated urea transport was strongly inhibited by this compound. Thus, this amphibian urea transporter displays transport characteristics in between those of UT-A2 and UT-B.
Elsevier