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Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import
Toc75 plays a central role in chloroplast biogenesis in plants as the membrane channel of the protein import translocon at the outer envelope of chloroplasts (TOC). Toc75 is a member of the Omp85 family of bacterial and organellar membrane insertases, characterized by N-terminal POTRA (polypeptide-t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811774/ https://www.ncbi.nlm.nih.gov/pubmed/26999824 http://dx.doi.org/10.7554/eLife.12631 |
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author | Paila, Yamuna D Richardson, Lynn GL Inoue, Hitoshi Parks, Elizabeth S McMahon, James Inoue, Kentaro Schnell, Danny J |
author_facet | Paila, Yamuna D Richardson, Lynn GL Inoue, Hitoshi Parks, Elizabeth S McMahon, James Inoue, Kentaro Schnell, Danny J |
author_sort | Paila, Yamuna D |
collection | PubMed |
description | Toc75 plays a central role in chloroplast biogenesis in plants as the membrane channel of the protein import translocon at the outer envelope of chloroplasts (TOC). Toc75 is a member of the Omp85 family of bacterial and organellar membrane insertases, characterized by N-terminal POTRA (polypeptide-transport associated) domains and C-terminal membrane-integrated β-barrels. We demonstrate that the Toc75 POTRA domains are essential for protein import and contribute to interactions with TOC receptors, thereby coupling preprotein recognition at the chloroplast surface with membrane translocation. The POTRA domains also interact with preproteins and mediate the recruitment of molecular chaperones in the intermembrane space to facilitate membrane transport. Our studies are consistent with the multi-functional roles of POTRA domains observed in other Omp85 family members and demonstrate that the domains of Toc75 have evolved unique properties specific to the acquisition of protein import during endosymbiotic evolution of the TOC system in plastids. DOI: http://dx.doi.org/10.7554/eLife.12631.001 |
format | Online Article Text |
id | pubmed-4811774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48117742016-04-04 Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import Paila, Yamuna D Richardson, Lynn GL Inoue, Hitoshi Parks, Elizabeth S McMahon, James Inoue, Kentaro Schnell, Danny J eLife Cell Biology Toc75 plays a central role in chloroplast biogenesis in plants as the membrane channel of the protein import translocon at the outer envelope of chloroplasts (TOC). Toc75 is a member of the Omp85 family of bacterial and organellar membrane insertases, characterized by N-terminal POTRA (polypeptide-transport associated) domains and C-terminal membrane-integrated β-barrels. We demonstrate that the Toc75 POTRA domains are essential for protein import and contribute to interactions with TOC receptors, thereby coupling preprotein recognition at the chloroplast surface with membrane translocation. The POTRA domains also interact with preproteins and mediate the recruitment of molecular chaperones in the intermembrane space to facilitate membrane transport. Our studies are consistent with the multi-functional roles of POTRA domains observed in other Omp85 family members and demonstrate that the domains of Toc75 have evolved unique properties specific to the acquisition of protein import during endosymbiotic evolution of the TOC system in plastids. DOI: http://dx.doi.org/10.7554/eLife.12631.001 eLife Sciences Publications, Ltd 2016-03-21 /pmc/articles/PMC4811774/ /pubmed/26999824 http://dx.doi.org/10.7554/eLife.12631 Text en © 2016, Paila et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Paila, Yamuna D Richardson, Lynn GL Inoue, Hitoshi Parks, Elizabeth S McMahon, James Inoue, Kentaro Schnell, Danny J Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import |
title | Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import |
title_full | Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import |
title_fullStr | Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import |
title_full_unstemmed | Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import |
title_short | Multi-functional roles for the polypeptide transport associated domains of Toc75 in chloroplast protein import |
title_sort | multi-functional roles for the polypeptide transport associated domains of toc75 in chloroplast protein import |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811774/ https://www.ncbi.nlm.nih.gov/pubmed/26999824 http://dx.doi.org/10.7554/eLife.12631 |
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