Transcriptome analysis of embryonic and adult sensory axons reveals changes in mRNA repertoire localization

  1. James W. Fawcett1
  1. 1Centre for Brain Repair, University of Cambridge, Forvie Site, Cambridge CB2 0PY, United Kingdom
  2. 2University of Cambridge Metabolic Research Labs, Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom
  3. 3Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, United Kingdom
  4. 4Burke-Cornell Medical Research Institute, White Plains, New York 10605, USA
  5. 5Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, California 90095, USA
  6. 6Department of Biology, Drexel University, Philadelphia, Pennsylvania 19401, USA
  1. 7 These authors contributed equally to this work.

Abstract

mRNAs are transported, localized, and translated in axons of sensory neurons. However, little is known about the full repertoire of transcripts present in embryonic and adult sensory axons and how this pool of mRNAs dynamically changes during development. Here, we used a compartmentalized chamber to isolate mRNA from pure embryonic and adult sensory axons devoid of non-neuronal or cell body contamination. Genome-wide microarray analysis reveals that a previously unappreciated number of transcripts are localized in sensory axons and that this repertoire changes during development toward adulthood. Embryonic axons are enriched in transcripts encoding cytoskeletal-related proteins with a role in axonal outgrowth. Surprisingly, adult axons are enriched in mRNAs encoding immune molecules with a role in nociception. Additionally, we show Tubulin-beta3 (Tubb3) mRNA is present only in embryonic axons, with Tubb3 locally synthesized in axons of embryonic, but not adult neurons where it is transported, thus validating our experimental approach. In summary, we provide the first complete catalog of embryonic and adult sensory axonal mRNAs. In addition we show that this pool of axonal mRNAs dynamically changes during development. These data provide an important resource for studies on the role of local protein synthesis in axon regeneration and nociception during neuronal development.

Keywords

Footnotes

  • Reprint requests to: James W. Fawcett, Centre for Brain Repair, University of Cambridge, Forvie Site, Robinson Way, Cambridge CB2 0PY, U.K.; e-mail: jf108{at}cam.ac.uk; fax: (44) 1223-331174; or Giles S.H. Yeo, University of Cambridge Metabolic Research Labs, Level 4, Institute of Metabolic Science, Box 289, Addenbrooke's Hospital, Cambridge CB2 0QQ, UK; e-mail: gshy2{at}cam.ac.uk; fax: (44) 1223-330598.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.2386111.

  • Received July 22, 2010.
  • Accepted October 21, 2010.
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