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Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels
Phosphatidic acid (PA) is postulated to have both structural and signaling functions during membrane dynamics in animal cells. In this study, we show that before a critical time period during rhabdomere biogenesis in Drosophila melanogaster photoreceptors, elevated levels of PA disrupt membrane tran...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700502/ https://www.ncbi.nlm.nih.gov/pubmed/19349583 http://dx.doi.org/10.1083/jcb.200807027 |
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author | Raghu, Padinjat Coessens, Elise Manifava, Maria Georgiev, Plamen Pettitt, Trevor Wood, Eleanor Garcia-Murillas, Isaac Okkenhaug, Hanneke Trivedi, Deepti Zhang, Qifeng Razzaq, Azam Zaid, Ola Wakelam, Michael O'Kane, Cahir J Ktistakis, Nicholas |
author_facet | Raghu, Padinjat Coessens, Elise Manifava, Maria Georgiev, Plamen Pettitt, Trevor Wood, Eleanor Garcia-Murillas, Isaac Okkenhaug, Hanneke Trivedi, Deepti Zhang, Qifeng Razzaq, Azam Zaid, Ola Wakelam, Michael O'Kane, Cahir J Ktistakis, Nicholas |
author_sort | Raghu, Padinjat |
collection | PubMed |
description | Phosphatidic acid (PA) is postulated to have both structural and signaling functions during membrane dynamics in animal cells. In this study, we show that before a critical time period during rhabdomere biogenesis in Drosophila melanogaster photoreceptors, elevated levels of PA disrupt membrane transport to the apical domain. Lipidomic analysis shows that this effect is associated with an increase in the abundance of a single, relatively minor molecular species of PA. These transport defects are dependent on the activation state of Arf1. Transport defects via PA generated by phospholipase D require the activity of type I phosphatidylinositol (PI) 4 phosphate 5 kinase, are phenocopied by knockdown of PI 4 kinase, and are associated with normal endoplasmic reticulum to Golgi transport. We propose that PA levels are critical for apical membrane transport events required for rhabdomere biogenesis. |
format | Text |
id | pubmed-2700502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27005022009-10-06 Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels Raghu, Padinjat Coessens, Elise Manifava, Maria Georgiev, Plamen Pettitt, Trevor Wood, Eleanor Garcia-Murillas, Isaac Okkenhaug, Hanneke Trivedi, Deepti Zhang, Qifeng Razzaq, Azam Zaid, Ola Wakelam, Michael O'Kane, Cahir J Ktistakis, Nicholas J Cell Biol Research Articles Phosphatidic acid (PA) is postulated to have both structural and signaling functions during membrane dynamics in animal cells. In this study, we show that before a critical time period during rhabdomere biogenesis in Drosophila melanogaster photoreceptors, elevated levels of PA disrupt membrane transport to the apical domain. Lipidomic analysis shows that this effect is associated with an increase in the abundance of a single, relatively minor molecular species of PA. These transport defects are dependent on the activation state of Arf1. Transport defects via PA generated by phospholipase D require the activity of type I phosphatidylinositol (PI) 4 phosphate 5 kinase, are phenocopied by knockdown of PI 4 kinase, and are associated with normal endoplasmic reticulum to Golgi transport. We propose that PA levels are critical for apical membrane transport events required for rhabdomere biogenesis. The Rockefeller University Press 2009-04-06 /pmc/articles/PMC2700502/ /pubmed/19349583 http://dx.doi.org/10.1083/jcb.200807027 Text en © 2009 Raghu et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Raghu, Padinjat Coessens, Elise Manifava, Maria Georgiev, Plamen Pettitt, Trevor Wood, Eleanor Garcia-Murillas, Isaac Okkenhaug, Hanneke Trivedi, Deepti Zhang, Qifeng Razzaq, Azam Zaid, Ola Wakelam, Michael O'Kane, Cahir J Ktistakis, Nicholas Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
title | Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
title_full | Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
title_fullStr | Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
title_full_unstemmed | Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
title_short | Rhabdomere biogenesis in Drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
title_sort | rhabdomere biogenesis in drosophila photoreceptors is acutely sensitive to phosphatidic acid levels |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700502/ https://www.ncbi.nlm.nih.gov/pubmed/19349583 http://dx.doi.org/10.1083/jcb.200807027 |
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