Regulation of axonal trafficking of cytochrome c oxidase IV mRNA

Mol Cell Neurosci. 2010 Apr;43(4):422-30. doi: 10.1016/j.mcn.2010.01.009. Epub 2010 Feb 6.

Abstract

Trafficking and local translation of axonal mRNAs play a critical role in the development and function of this neuronal subcellular structural domain. In this report, we studied cytochrome c oxidase subunit IV (COXIV) mRNA trafficking into distal axons of primary superior cervical ganglia (SCG) neurons, and provided evidence that axonal trafficking and mitochondrial association of the mRNA are mediated by an element located in a 38bp-long, hairpin-loop forming region within the 3'UTR of the transcript. Our results also suggest that suppression of local translation of COXIV mRNA results in significant attenuation of axonal elongation. Taken together, the results provide the first evidence for the existence of a cis-acting axonal transport element within a nuclear-encoding mitochondrial gene, and demonstrate the importance of the axonal trafficking and local translation of nuclear-encoded mitochondrial mRNAs in axonal growth.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Analysis of Variance
  • Animals
  • Animals, Newborn
  • Axonal Transport / physiology*
  • Axons / metabolism
  • Blotting, Western
  • Cell Nucleus / genetics
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism*
  • In Situ Hybridization
  • Mitochondria / metabolism
  • Neurons / cytology
  • Neurons / metabolism*
  • RNA Interference
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superior Cervical Ganglion / cytology
  • Superior Cervical Ganglion / metabolism*

Substances

  • RNA, Messenger
  • RNA, Small Interfering
  • Electron Transport Complex IV