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Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration
Neuronal growth cones are essential for nerve growth and regeneration, as well as for the formation and rearrangement of the neural network. To elucidate phosphorylation-dependent signaling pathways and establish useful molecular markers for axon growth and regeneration, we performed a phosphoproteo...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147025/ https://www.ncbi.nlm.nih.gov/pubmed/30240740 http://dx.doi.org/10.1016/j.isci.2018.05.019 |
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author | Kawasaki, Asami Okada, Masayasu Tamada, Atsushi Okuda, Shujiro Nozumi, Motohiro Ito, Yasuyuki Kobayashi, Daiki Yamasaki, Tokiwa Yokoyama, Ryo Shibata, Takeshi Nishina, Hiroshi Yoshida, Yutaka Fujii, Yukihiko Takeuchi, Kosei Igarashi, Michihiro |
author_facet | Kawasaki, Asami Okada, Masayasu Tamada, Atsushi Okuda, Shujiro Nozumi, Motohiro Ito, Yasuyuki Kobayashi, Daiki Yamasaki, Tokiwa Yokoyama, Ryo Shibata, Takeshi Nishina, Hiroshi Yoshida, Yutaka Fujii, Yukihiko Takeuchi, Kosei Igarashi, Michihiro |
author_sort | Kawasaki, Asami |
collection | PubMed |
description | Neuronal growth cones are essential for nerve growth and regeneration, as well as for the formation and rearrangement of the neural network. To elucidate phosphorylation-dependent signaling pathways and establish useful molecular markers for axon growth and regeneration, we performed a phosphoproteomics study of mammalian growth cones, which identified >30,000 phosphopeptides of ∼1,200 proteins. The phosphorylation sites were highly proline directed and primarily MAPK dependent, owing to the activation of JNK, suggesting that proteins that undergo proline-directed phosphorylation mediate nerve growth in the mammalian brain. Bioinformatics analysis revealed that phosphoproteins were enriched in microtubules and the cortical cytoskeleton. The most frequently phosphorylated site was S96 of GAP-43 (growth-associated protein 43-kDa), a vertebrate-specific protein involved in axon growth. This previously uncharacterized phosphorylation site was JNK dependent. S96 phosphorylation was specifically detected in growing and regenerating axons as the most frequent target of JNK signaling; thus it represents a promising new molecular marker for mammalian axonal growth and regeneration. |
format | Online Article Text |
id | pubmed-6147025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61470252018-10-02 Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration Kawasaki, Asami Okada, Masayasu Tamada, Atsushi Okuda, Shujiro Nozumi, Motohiro Ito, Yasuyuki Kobayashi, Daiki Yamasaki, Tokiwa Yokoyama, Ryo Shibata, Takeshi Nishina, Hiroshi Yoshida, Yutaka Fujii, Yukihiko Takeuchi, Kosei Igarashi, Michihiro iScience Article Neuronal growth cones are essential for nerve growth and regeneration, as well as for the formation and rearrangement of the neural network. To elucidate phosphorylation-dependent signaling pathways and establish useful molecular markers for axon growth and regeneration, we performed a phosphoproteomics study of mammalian growth cones, which identified >30,000 phosphopeptides of ∼1,200 proteins. The phosphorylation sites were highly proline directed and primarily MAPK dependent, owing to the activation of JNK, suggesting that proteins that undergo proline-directed phosphorylation mediate nerve growth in the mammalian brain. Bioinformatics analysis revealed that phosphoproteins were enriched in microtubules and the cortical cytoskeleton. The most frequently phosphorylated site was S96 of GAP-43 (growth-associated protein 43-kDa), a vertebrate-specific protein involved in axon growth. This previously uncharacterized phosphorylation site was JNK dependent. S96 phosphorylation was specifically detected in growing and regenerating axons as the most frequent target of JNK signaling; thus it represents a promising new molecular marker for mammalian axonal growth and regeneration. Elsevier 2018-05-31 /pmc/articles/PMC6147025/ /pubmed/30240740 http://dx.doi.org/10.1016/j.isci.2018.05.019 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kawasaki, Asami Okada, Masayasu Tamada, Atsushi Okuda, Shujiro Nozumi, Motohiro Ito, Yasuyuki Kobayashi, Daiki Yamasaki, Tokiwa Yokoyama, Ryo Shibata, Takeshi Nishina, Hiroshi Yoshida, Yutaka Fujii, Yukihiko Takeuchi, Kosei Igarashi, Michihiro Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration |
title | Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration |
title_full | Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration |
title_fullStr | Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration |
title_full_unstemmed | Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration |
title_short | Growth Cone Phosphoproteomics Reveals that GAP-43 Phosphorylated by JNK Is a Marker of Axon Growth and Regeneration |
title_sort | growth cone phosphoproteomics reveals that gap-43 phosphorylated by jnk is a marker of axon growth and regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147025/ https://www.ncbi.nlm.nih.gov/pubmed/30240740 http://dx.doi.org/10.1016/j.isci.2018.05.019 |
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