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Characterization of TSET, an ancient and widespread membrane trafficking complex
The heterotetrameric AP and F-COPI complexes help to define the cellular map of modern eukaryotes. To search for related machinery, we developed a structure-based bioinformatics tool, and identified the core subunits of TSET, a 'missing link' between the APs and COPI. Studies in Dictyostel...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031984/ https://www.ncbi.nlm.nih.gov/pubmed/24867644 http://dx.doi.org/10.7554/eLife.02866 |
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author | Hirst, Jennifer Schlacht, Alexander Norcott, John P Traynor, David Bloomfield, Gareth Antrobus, Robin Kay, Robert R Dacks, Joel B Robinson, Margaret S |
author_facet | Hirst, Jennifer Schlacht, Alexander Norcott, John P Traynor, David Bloomfield, Gareth Antrobus, Robin Kay, Robert R Dacks, Joel B Robinson, Margaret S |
author_sort | Hirst, Jennifer |
collection | PubMed |
description | The heterotetrameric AP and F-COPI complexes help to define the cellular map of modern eukaryotes. To search for related machinery, we developed a structure-based bioinformatics tool, and identified the core subunits of TSET, a 'missing link' between the APs and COPI. Studies in Dictyostelium indicate that TSET is a heterohexamer, with two associated scaffolding proteins. TSET is non-essential in Dictyostelium, but may act in plasma membrane turnover, and is essentially identical to the recently described TPLATE complex, TPC. However, whereas TPC was reported to be plant-specific, we can identify a full or partial complex in every eukaryotic supergroup. An evolutionary path can be deduced from the earliest origins of the heterotetramer/scaffold coat to its multiple manifestations in modern organisms, including the mammalian muniscins, descendants of the TSET medium subunits. Thus, we have uncovered the machinery for an ancient and widespread pathway, which provides new insights into early eukaryotic evolution. DOI: http://dx.doi.org/10.7554/eLife.02866.001 |
format | Online Article Text |
id | pubmed-4031984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40319842014-06-02 Characterization of TSET, an ancient and widespread membrane trafficking complex Hirst, Jennifer Schlacht, Alexander Norcott, John P Traynor, David Bloomfield, Gareth Antrobus, Robin Kay, Robert R Dacks, Joel B Robinson, Margaret S eLife Cell Biology The heterotetrameric AP and F-COPI complexes help to define the cellular map of modern eukaryotes. To search for related machinery, we developed a structure-based bioinformatics tool, and identified the core subunits of TSET, a 'missing link' between the APs and COPI. Studies in Dictyostelium indicate that TSET is a heterohexamer, with two associated scaffolding proteins. TSET is non-essential in Dictyostelium, but may act in plasma membrane turnover, and is essentially identical to the recently described TPLATE complex, TPC. However, whereas TPC was reported to be plant-specific, we can identify a full or partial complex in every eukaryotic supergroup. An evolutionary path can be deduced from the earliest origins of the heterotetramer/scaffold coat to its multiple manifestations in modern organisms, including the mammalian muniscins, descendants of the TSET medium subunits. Thus, we have uncovered the machinery for an ancient and widespread pathway, which provides new insights into early eukaryotic evolution. DOI: http://dx.doi.org/10.7554/eLife.02866.001 eLife Sciences Publications, Ltd 2014-05-27 /pmc/articles/PMC4031984/ /pubmed/24867644 http://dx.doi.org/10.7554/eLife.02866 Text en © 2014, Hirst et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Hirst, Jennifer Schlacht, Alexander Norcott, John P Traynor, David Bloomfield, Gareth Antrobus, Robin Kay, Robert R Dacks, Joel B Robinson, Margaret S Characterization of TSET, an ancient and widespread membrane trafficking complex |
title | Characterization of TSET, an ancient and widespread membrane trafficking complex |
title_full | Characterization of TSET, an ancient and widespread membrane trafficking complex |
title_fullStr | Characterization of TSET, an ancient and widespread membrane trafficking complex |
title_full_unstemmed | Characterization of TSET, an ancient and widespread membrane trafficking complex |
title_short | Characterization of TSET, an ancient and widespread membrane trafficking complex |
title_sort | characterization of tset, an ancient and widespread membrane trafficking complex |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4031984/ https://www.ncbi.nlm.nih.gov/pubmed/24867644 http://dx.doi.org/10.7554/eLife.02866 |
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