Functional analysis of human cardiac gap junction channel mutants

Glenn I. Fishman, Alonso P. Moreno, David C. Spray, Leslie A. Leinwand

Research output: Contribution to journalArticle

114 Citations (Scopus)

Abstract

The connexins form a family of membrane spanning proteins that assemble into gap junction channels. The biophysical properties of these channels are dependent upon the constituent connexin isoform. To begin identifying the molecular basis for gap junction channel behavior in the human heart, a tissue that expresses connexin43, we used site-directed mutagenesis to generate mutant cDNAs of human connexin43 with shortened cytoplasmic tail domains. Premature stop codons were inserted, resulting in proteins corresponding in length to the mammalian isoforms connexin32 and connexin26, which are expressed primarily in liver. All constructs restore intercellular coupling when they are transfected into SKHep1 cells, a human hepatoma line that is communication deficient. Whereas wild-type connexin43 transfectants display two distinct unitary conductance values of about 60 and 100 pS, transfectants expressing the mutant proteins, from which 80 and 138 amino acids have been deleted, exhibit markedly different single-channel properties, with unitary conductance values of about 160 and 50 pS, respectively, .functional conductance of channels composed of wild-type connexin43 is less voltage-sensitive compared with transfectants expressing wild-type connexin32. However, neither of the connexin43 truncation mutants alters this relative voltage insensitivity. These results suggest that the cytoplasmic tail domain is an important determinant of the unitary conductance event of gap junction channels but not their voltage dependence. Furthermore, since the mutant connexins are missing several consensus phosphorylation sites, modification of these particular sites may not be required for membrane insertion or assembly of human connexin43 into functional channels.

Original languageEnglish (US)
Pages (from-to)3525-3529
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume88
Issue number9
StatePublished - 1991

Fingerprint

Connexin 43
Gap Junctions
Connexins
Tail
Protein Isoforms
Nonsense Codon
Mutant Proteins
Site-Directed Mutagenesis
Hepatocellular Carcinoma
Membrane Proteins
Complementary DNA
Communication
Phosphorylation
Amino Acids
Membranes
Liver
Proteins

Keywords

  • Connexin
  • Electrophysiology
  • Heart
  • Single channels
  • SKHep1 cells

ASJC Scopus subject areas

  • General
  • Genetics

Cite this

Functional analysis of human cardiac gap junction channel mutants. / Fishman, Glenn I.; Moreno, Alonso P.; Spray, David C.; Leinwand, Leslie A.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 88, No. 9, 1991, p. 3525-3529.

Research output: Contribution to journalArticle

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