Functional features of the "finger" domain of the DEG/ENaC channels MEC-4 and UNC-8

Am J Physiol Cell Physiol. 2018 Aug 1;315(2):C155-C163. doi: 10.1152/ajpcell.00297.2017. Epub 2018 Apr 25.


UNC-8 and MEC-4 are two members of the degenerin/epithelial Na+ channel (DEG/ENaC) family of voltage-independent Na+ channels that share a high degree of sequence homology and functional similarity. For example, both can be hyperactivated by genetic mutations [UNC-8(d) and MEC-4(d)] that induce neuronal death by necrosis. Both depend in vivo on chaperone protein MEC-6 for function, as demonstrated by the finding that neuronal death induced by hyperactive UNC-8 and MEC-4 channels is prevented by null mutations in mec-6. UNC-8 and MEC-4 differ functionally in three major ways: 1) MEC-4 is calcium permeable, whereas UNC-8 is not; 2) UNC-8, but not MEC-4, is blocked by extracellular calcium and magnesium in the micromolar range; and 3) MEC-6 increases the number of MEC-4 channels at the cell surface in oocytes but does not have this effect on UNC-8. We previously reported that Ca2+permeability of MEC-4 is conferred by the second transmembrane domain. We show here that the extracellular "finger" domain of UNC-8 is sufficient to mediate inhibition by divalent cations and that regulation by MEC-6 also depends on this region. Thus, our work confirms that the finger domain houses residues involved in gating of this channel class and shows for the first time that the finger domain also mediates regulation by chaperone protein MEC-6. Given that the finger domain is the most divergent region across the DEG/ENaC family, we speculate that it influences channel trafficking and function in a unique manner depending on the channel subunit.

Keywords: DEG/ENaC channels; accessory proteins; divalent cations.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Calcium / metabolism
  • Cell Death / physiology
  • Cell Membrane Permeability / physiology
  • Epithelial Sodium Channels / metabolism*
  • Magnesium / metabolism
  • Membrane Proteins / metabolism*
  • Mutation / physiology
  • Oocytes / metabolism
  • Protein Transport / physiology
  • Sodium / metabolism*
  • Xenopus laevis / metabolism


  • Epithelial Sodium Channels
  • Membrane Proteins
  • Sodium
  • Magnesium
  • Calcium