Cystic fibrosis gene expression is not correlated with rectifying Cl sup minus channels
- Stanford Univ., CA (United States)
- Univ. of California, San Francisco (United States)
Cystic fibrosis (CF) involves a profound reduction of Cl{sup {minus}} permeability in several exocrine tissues. A distinctive, outwardly rectifying, depolarization-induced Cl{sup {minus}} channel (ORDIC channel) has been proposed to account for the Cl{sup {minus}} conductance that is defective in CF. The recently identified CF gene is predicted to code for a 1480-amino acid integral membrane protein termed the CF transmembrane conductance regulator (CFTR). The CFTR shares sequence similarity with a superfamily of ATP-binding membrane transport proteins such as P-glycoprotein and STE6, but it also has features consistent with an ion channel function. It has been proposed that the CFTR might be an ORDIC channel. To determine if CFTR and ORDIC channel expression are correlated, the authors surveyed various cell lines for natural variation in CFTR and ORDIC channel expression. In four human epithelial cell lines (T84, CaCo2, PANC-1, and 9HTEo-/S) that encompass the full observed range of CFTR mRNA levels and ORDIC channel density the authors found no correlation.
- OSTI ID:
- 6101184
- Journal Information:
- Proceedings of the National Academy of Sciences of the United States of America; (United States), Vol. 88:12; ISSN 0027-8424
- Country of Publication:
- United States
- Language:
- English
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CHLORIDES
MEMBRANE TRANSPORT
HEREDITARY DISEASES
ETIOLOGY
DNA POLYMERASES
EPITHELIUM
FIBROSIS
GENE REGULATION
MAN
MESSENGER-RNA
PERMEABILITY
ANIMAL TISSUES
ANIMALS
BODY
CHLORINE COMPOUNDS
DISEASES
ENZYMES
HALIDES
HALOGEN COMPOUNDS
MAMMALS
NUCLEIC ACIDS
NUCLEOTIDYLTRANSFERASES
ORGANIC COMPOUNDS
PATHOLOGICAL CHANGES
PHOSPHORUS-GROUP TRANSFERASES
POLYMERASES
PRIMATES
PROTEINS
RNA
TISSUES
TRANSFERASES
VERTEBRATES
550200* - Biochemistry