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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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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. |
format | Online Article Text |
id | pubmed-3904817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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