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DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia
The morphogenic factor Sonic hedgehog (Shh) signals through the primary cilium, which relies on intraflagellar transport to maintain its structural integrity and function. However, the process by which protein and lipid cargos are delivered to the primary cilium from their sites of synthesis still r...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509727/ https://www.ncbi.nlm.nih.gov/pubmed/28706295 http://dx.doi.org/10.1038/s41598-017-05680-8 |
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author | Ding, Jie Shao, Lei Yao, Yixing Tong, Xin Liu, Huaize Yue, Shen Xie, Lu Cheng, Steven Y. |
author_facet | Ding, Jie Shao, Lei Yao, Yixing Tong, Xin Liu, Huaize Yue, Shen Xie, Lu Cheng, Steven Y. |
author_sort | Ding, Jie |
collection | PubMed |
description | The morphogenic factor Sonic hedgehog (Shh) signals through the primary cilium, which relies on intraflagellar transport to maintain its structural integrity and function. However, the process by which protein and lipid cargos are delivered to the primary cilium from their sites of synthesis still remains poorly characterized. Here, we report that diacylglycerol kinase δ (DGKδ), a residential lipid kinase in the endoplasmic reticulum, triggers the release of IFT88-containing vesicles from the ER exit sites (ERES), thereby setting forth their movement to the primary cilium. Encoded by the gene whose mutations originally implicated the primary cilium as the venue of Shh signaling, IFT88 is known to be part of the complex B that drives the anterograde transport within cilia. We show that IFT88 interacts with DGKδ, and is associated with COPII-coated vesicles at the ERES. Using a combination of RNAi silencing and gene knockout strategies, we further show that DGKδ is required for supporting Shh signaling both in vitro and in vivo, demonstrating the physiological significance of this regulation. |
format | Online Article Text |
id | pubmed-5509727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55097272017-07-17 DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia Ding, Jie Shao, Lei Yao, Yixing Tong, Xin Liu, Huaize Yue, Shen Xie, Lu Cheng, Steven Y. Sci Rep Article The morphogenic factor Sonic hedgehog (Shh) signals through the primary cilium, which relies on intraflagellar transport to maintain its structural integrity and function. However, the process by which protein and lipid cargos are delivered to the primary cilium from their sites of synthesis still remains poorly characterized. Here, we report that diacylglycerol kinase δ (DGKδ), a residential lipid kinase in the endoplasmic reticulum, triggers the release of IFT88-containing vesicles from the ER exit sites (ERES), thereby setting forth their movement to the primary cilium. Encoded by the gene whose mutations originally implicated the primary cilium as the venue of Shh signaling, IFT88 is known to be part of the complex B that drives the anterograde transport within cilia. We show that IFT88 interacts with DGKδ, and is associated with COPII-coated vesicles at the ERES. Using a combination of RNAi silencing and gene knockout strategies, we further show that DGKδ is required for supporting Shh signaling both in vitro and in vivo, demonstrating the physiological significance of this regulation. Nature Publishing Group UK 2017-07-13 /pmc/articles/PMC5509727/ /pubmed/28706295 http://dx.doi.org/10.1038/s41598-017-05680-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ding, Jie Shao, Lei Yao, Yixing Tong, Xin Liu, Huaize Yue, Shen Xie, Lu Cheng, Steven Y. DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia |
title | DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia |
title_full | DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia |
title_fullStr | DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia |
title_full_unstemmed | DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia |
title_short | DGKδ triggers endoplasmic reticulum release of IFT88-containing vesicles destined for the assembly of primary cilia |
title_sort | dgkδ triggers endoplasmic reticulum release of ift88-containing vesicles destined for the assembly of primary cilia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509727/ https://www.ncbi.nlm.nih.gov/pubmed/28706295 http://dx.doi.org/10.1038/s41598-017-05680-8 |
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