Cx23, a connexin with only four extracellular-loop cysteines, forms functional gap junction channels and hemichannels

FEBS Lett. 2008 Jan 23;582(2):165-70. doi: 10.1016/j.febslet.2007.11.079. Epub 2007 Dec 7.

Abstract

Gap junction channels may be comprised of either connexin or pannexin proteins (innexins and pannexins). Membrane topologies of both families are similar, but sequence similarity is lacking. Recently, connexin-like sequences have been identified in mammalian and zebrafish genomes that have only four conserved cysteines in the extracellular domains (Cx23), a feature of the pannexins. Phylogenetic analyses of the non-canonical "C4" connexins reveal that these sequences are indeed connexins. Functional assays reveal that the Cx23 gap junctions are capable of sharing neurobiotin, and further, that Cx23 connexins form hemichannels in vitro.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Connexins / chemistry
  • Connexins / physiology*
  • Cysteine / chemistry*
  • DNA Primers
  • Gap Junctions / chemistry
  • Gap Junctions / physiology*
  • HeLa Cells
  • Humans
  • In Situ Hybridization
  • Lens, Crystalline / metabolism
  • Molecular Sequence Data
  • Sequence Homology, Amino Acid
  • Zebrafish

Substances

  • Connexins
  • DNA Primers
  • Cysteine