Molecular cloning and transmembrane structure of hCLCA2 from human lung, trachea, and mammary gland

Am J Physiol. 1999 Jun;276(6):C1261-70. doi: 10.1152/ajpcell.1999.276.6.C1261.

Abstract

The CLCA family of Ca2+-activated Cl- channels has recently been discovered, with an increasing number of closely related members isolated from different species. Here we report the cloning of the second human homolog, hCLCA2, from a human lung cDNA library. Northern blot and RT-PCR analyses revealed additional expression in trachea and mammary gland. A primary translation product of 120 kDa was cleaved into two cell surface-associated glycoproteins of 86 and 34 kDa in transfected HEK-293 cells. hCLCA2 is the first CLCA homolog for which the transmembrane structure has been systematically studied. Glycosylation site scanning and protease protection assays revealed five transmembrane domains with a large, cysteine-rich, amino-terminal extracellular domain. Whole cell patch-clamp recordings of hCLCA2-transfected HEK-293 cells detected a slightly outwardly rectifying anion conductance that was increased in the presence of the Ca2+ ionophore ionomycin and inhibited by DIDS, dithiothreitol, niflumic acid, and tamoxifen. Expression in human trachea and lung suggests that hCLCA2 may play a role in the complex pathogenesis of cystic fibrosis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence / genetics
  • Base Sequence / genetics
  • Breast / metabolism*
  • Cell Line
  • Chloride Channels / chemistry*
  • Chloride Channels / genetics*
  • Chloride Channels / metabolism
  • Chloride Channels / physiology
  • Cloning, Molecular*
  • DNA, Complementary / genetics
  • Electrophysiology
  • Female
  • Humans
  • Lung / metabolism*
  • Molecular Sequence Data
  • Trachea / metabolism*

Substances

  • CLCA2 protein, human
  • Chloride Channels
  • DNA, Complementary

Associated data

  • GENBANK/AF043977