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Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11

Vesicular trafficking plays a key role in tuning the activity of Notch signaling. Here, we describe a novel and conserved Rab geranylgeranyltransferase (RabGGT)-α–like subunit that is required for Notch signaling-mediated lateral inhibition and cell fate determination of external sensory organs. Thi...

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Autores principales: Charng, Wu-Lin, Yamamoto, Shinya, Jaiswal, Manish, Bayat, Vafa, Xiong, Bo, Zhang, Ke, Sandoval, Hector, David, Gabriela, Gibbs, Stephen, Lu, Hsiang-Chih, Chen, Kuchuan, Giagtzoglou, Nikos, Bellen, Hugo J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904817/
https://www.ncbi.nlm.nih.gov/pubmed/24492843
http://dx.doi.org/10.1371/journal.pbio.1001777
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author Charng, Wu-Lin
Yamamoto, Shinya
Jaiswal, Manish
Bayat, Vafa
Xiong, Bo
Zhang, Ke
Sandoval, Hector
David, Gabriela
Gibbs, Stephen
Lu, Hsiang-Chih
Chen, Kuchuan
Giagtzoglou, Nikos
Bellen, Hugo J.
author_facet Charng, Wu-Lin
Yamamoto, Shinya
Jaiswal, Manish
Bayat, Vafa
Xiong, Bo
Zhang, Ke
Sandoval, Hector
David, Gabriela
Gibbs, Stephen
Lu, Hsiang-Chih
Chen, Kuchuan
Giagtzoglou, Nikos
Bellen, Hugo J.
author_sort Charng, Wu-Lin
collection PubMed
description Vesicular trafficking plays a key role in tuning the activity of Notch signaling. Here, we describe a novel and conserved Rab geranylgeranyltransferase (RabGGT)-α–like subunit that is required for Notch signaling-mediated lateral inhibition and cell fate determination of external sensory organs. This protein is encoded by tempura, and its loss affects the secretion of Scabrous and Delta, two proteins required for proper Notch signaling. We show that Tempura forms a heretofore uncharacterized RabGGT complex that geranylgeranylates Rab1 and Rab11. This geranylgeranylation is required for their proper subcellular localization. A partial dysfunction of Rab1 affects Scabrous and Delta in the secretory pathway. In addition, a partial loss Rab11 affects trafficking of Delta. In summary, Tempura functions as a new geranylgeranyltransferase that regulates the subcellular localization of Rab1 and Rab11, which in turn regulate trafficking of Scabrous and Delta, thereby affecting Notch signaling.
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spelling pubmed-39048172014-01-31 Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11 Charng, Wu-Lin Yamamoto, Shinya Jaiswal, Manish Bayat, Vafa Xiong, Bo Zhang, Ke Sandoval, Hector David, Gabriela Gibbs, Stephen Lu, Hsiang-Chih Chen, Kuchuan Giagtzoglou, Nikos Bellen, Hugo J. PLoS Biol Research Article Vesicular trafficking plays a key role in tuning the activity of Notch signaling. Here, we describe a novel and conserved Rab geranylgeranyltransferase (RabGGT)-α–like subunit that is required for Notch signaling-mediated lateral inhibition and cell fate determination of external sensory organs. This protein is encoded by tempura, and its loss affects the secretion of Scabrous and Delta, two proteins required for proper Notch signaling. We show that Tempura forms a heretofore uncharacterized RabGGT complex that geranylgeranylates Rab1 and Rab11. This geranylgeranylation is required for their proper subcellular localization. A partial dysfunction of Rab1 affects Scabrous and Delta in the secretory pathway. In addition, a partial loss Rab11 affects trafficking of Delta. In summary, Tempura functions as a new geranylgeranyltransferase that regulates the subcellular localization of Rab1 and Rab11, which in turn regulate trafficking of Scabrous and Delta, thereby affecting Notch signaling. Public Library of Science 2014-01-28 /pmc/articles/PMC3904817/ /pubmed/24492843 http://dx.doi.org/10.1371/journal.pbio.1001777 Text en © 2014 Charng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Charng, Wu-Lin
Yamamoto, Shinya
Jaiswal, Manish
Bayat, Vafa
Xiong, Bo
Zhang, Ke
Sandoval, Hector
David, Gabriela
Gibbs, Stephen
Lu, Hsiang-Chih
Chen, Kuchuan
Giagtzoglou, Nikos
Bellen, Hugo J.
Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11
title Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11
title_full Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11
title_fullStr Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11
title_full_unstemmed Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11
title_short Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11
title_sort drosophila tempura, a novel protein prenyltransferase α subunit, regulates notch signaling via rab1 and rab11
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904817/
https://www.ncbi.nlm.nih.gov/pubmed/24492843
http://dx.doi.org/10.1371/journal.pbio.1001777
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