Frontiers in Physiology (Nov 2017)

Cx43 Isoform GJA1-20k Promotes Microtubule Dependent Mitochondrial Transport

  • Ying Fu,
  • Shan-Shan Zhang,
  • Shaohua Xiao,
  • Wassim A. Basheer,
  • Rachel Baum,
  • Irina Epifantseva,
  • TingTing Hong,
  • TingTing Hong,
  • Robin M. Shaw,
  • Robin M. Shaw

DOI
https://doi.org/10.3389/fphys.2017.00905
Journal volume & issue
Vol. 8

Abstract

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Connexin 43 (Cx43, encoded by GJA1) is a cell-cell communication gap junction protein expressed in all organ systems. It was recently found that GJA1 mRNA undergoes alternative translation to generate N-terminal truncated isoforms, of which GJA1-20k is the most abundant. Here we report a surprising finding that, unlike full length GJA1-43k, GJA1-20k has a strong tropism for mitochondria. Exploring function, we found that GJA1-20k appears to be an organelle chaperone and that overexpression of GJA1-20k is sufficient to rescue mitochondrial localization to the cell periphery upon exposure to hydrogen peroxide, which effectively limits the network fragmentation that occurs with oxidative stress. By high-resolution fluorescent imaging and electron microscopy, we determined that GJA1-20k is enriched at the interface between mitochondria and microtubules, appearing to load organelles for transport. Mutagenesis experiments revealed that although the microtubule-binding domain (MTBD) in GJA1-20k is not necessary for protein localization to mitochondria, the MTBD is essential for GJA1-20k to facilitate mitochondrial transport and maintain mitochondrial localization at the periphery. These results reveal an unexpected role for the alternatively translated isoform of the Cx43 gap junction protein, GJA1-20k, which is to facilitate microtubule-based mitochondrial transport and to maintain mitochondrial network integrity during cellular stress.

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