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Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation
Membrane association with mother centriole (M-centriole) distal appendages is critical for ciliogenesis initiation. How the Rab GTPase Rab11-Rab8 cascade functions in early ciliary membrane assembly is unknown. Here, we show that the membrane shaping proteins EHD1 and EHD3, in association with the R...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344897/ https://www.ncbi.nlm.nih.gov/pubmed/25686250 http://dx.doi.org/10.1038/ncb3109 |
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author | Lu, Quanlong Insinna, Christine Ott, Carolyn Stauffer, Jimmy Pintado, Petra A. Rahajeng, Juliati Baxa, Ulrich Walia, Vijay Cuenca, Adrian Hwang, Yoo-Seok Daar, Ira O. Lopes, Susana Lippincott-Schwartz, Jennifer Jackson, Peter K. Caplan, Steve Westlake, Christopher J. |
author_facet | Lu, Quanlong Insinna, Christine Ott, Carolyn Stauffer, Jimmy Pintado, Petra A. Rahajeng, Juliati Baxa, Ulrich Walia, Vijay Cuenca, Adrian Hwang, Yoo-Seok Daar, Ira O. Lopes, Susana Lippincott-Schwartz, Jennifer Jackson, Peter K. Caplan, Steve Westlake, Christopher J. |
author_sort | Lu, Quanlong |
collection | PubMed |
description | Membrane association with mother centriole (M-centriole) distal appendages is critical for ciliogenesis initiation. How the Rab GTPase Rab11-Rab8 cascade functions in early ciliary membrane assembly is unknown. Here, we show that the membrane shaping proteins EHD1 and EHD3, in association with the Rab11-Rab8 cascade, function in early ciliogenesis. EHD1 and EHD3 localize to pre-ciliary membranes and the ciliary pocket. EHD-dependent membrane tubulation is essential for ciliary vesicle (CV) formation from smaller distal appendage vesicles (DAV). Importantly, this step functions in M-centriole to basal body transformation and recruitment of transition zone proteins and IFT20. SNAP29, a SNARE membrane fusion regulator and EHD1-binding protein, is also required for DAV-mediated CV assembly. Interestingly, only after CV assembly is Rab8 activated for ciliary growth. Our studies uncover molecular mechanisms informing a previously uncharacterized ciliogenesis step whereby EHD1 and EHD3 reorganize the M-centriole and associated DAV prior to coordinated ciliary membrane and axoneme growth. |
format | Online Article Text |
id | pubmed-4344897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-43448972015-09-01 Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation Lu, Quanlong Insinna, Christine Ott, Carolyn Stauffer, Jimmy Pintado, Petra A. Rahajeng, Juliati Baxa, Ulrich Walia, Vijay Cuenca, Adrian Hwang, Yoo-Seok Daar, Ira O. Lopes, Susana Lippincott-Schwartz, Jennifer Jackson, Peter K. Caplan, Steve Westlake, Christopher J. Nat Cell Biol Article Membrane association with mother centriole (M-centriole) distal appendages is critical for ciliogenesis initiation. How the Rab GTPase Rab11-Rab8 cascade functions in early ciliary membrane assembly is unknown. Here, we show that the membrane shaping proteins EHD1 and EHD3, in association with the Rab11-Rab8 cascade, function in early ciliogenesis. EHD1 and EHD3 localize to pre-ciliary membranes and the ciliary pocket. EHD-dependent membrane tubulation is essential for ciliary vesicle (CV) formation from smaller distal appendage vesicles (DAV). Importantly, this step functions in M-centriole to basal body transformation and recruitment of transition zone proteins and IFT20. SNAP29, a SNARE membrane fusion regulator and EHD1-binding protein, is also required for DAV-mediated CV assembly. Interestingly, only after CV assembly is Rab8 activated for ciliary growth. Our studies uncover molecular mechanisms informing a previously uncharacterized ciliogenesis step whereby EHD1 and EHD3 reorganize the M-centriole and associated DAV prior to coordinated ciliary membrane and axoneme growth. 2015-02-16 2015-03 /pmc/articles/PMC4344897/ /pubmed/25686250 http://dx.doi.org/10.1038/ncb3109 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lu, Quanlong Insinna, Christine Ott, Carolyn Stauffer, Jimmy Pintado, Petra A. Rahajeng, Juliati Baxa, Ulrich Walia, Vijay Cuenca, Adrian Hwang, Yoo-Seok Daar, Ira O. Lopes, Susana Lippincott-Schwartz, Jennifer Jackson, Peter K. Caplan, Steve Westlake, Christopher J. Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation |
title | Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation |
title_full | Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation |
title_fullStr | Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation |
title_full_unstemmed | Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation |
title_short | Early steps in primary cilium assembly require EHD1- and EHD3-dependent ciliary vesicle formation |
title_sort | early steps in primary cilium assembly require ehd1- and ehd3-dependent ciliary vesicle formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344897/ https://www.ncbi.nlm.nih.gov/pubmed/25686250 http://dx.doi.org/10.1038/ncb3109 |
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