Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
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
_version_ 1783356498310594560
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
work_keys_str_mv AT kawasakiasami growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT okadamasayasu growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT tamadaatsushi growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT okudashujiro growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT nozumimotohiro growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT itoyasuyuki growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT kobayashidaiki growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT yamasakitokiwa growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT yokoyamaryo growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT shibatatakeshi growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT nishinahiroshi growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT yoshidayutaka growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT fujiiyukihiko growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT takeuchikosei growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration
AT igarashimichihiro growthconephosphoproteomicsrevealsthatgap43phosphorylatedbyjnkisamarkerofaxongrowthandregeneration