Molecular and functional characterization of an amphibian urea transporter

Biochim Biophys Acta. 1999 Oct 15;1421(2):347-52. doi: 10.1016/s0005-2736(99)00147-9.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / chemistry
  • Carrier Proteins / metabolism*
  • Cloning, Molecular
  • DNA, Complementary / chemistry
  • Gene Library
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / metabolism*
  • Membrane Transport Proteins*
  • Molecular Sequence Data
  • Oocytes
  • Rana esculenta
  • Sequence Alignment
  • Urea / metabolism*
  • Urea Transporters
  • Urinary Bladder / metabolism
  • Xenopus

Substances

  • Carrier Proteins
  • DNA, Complementary
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Urea

Associated data

  • GENBANK/Y12784