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How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies
BACKGROUND: It is commonly assumed that a heterotrophic ancestor of the supergroup Archaeplastida/Plantae engulfed a cyanobacterium that was transformed into a primary plastid; however, it is still unclear how nuclear-encoded proteins initially were imported into the new organelle. Most proteins tar...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716720/ https://www.ncbi.nlm.nih.gov/pubmed/23845039 http://dx.doi.org/10.1186/1745-6150-8-18 |
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author | Gagat, Przemysław Bodył, Andrzej Mackiewicz, Paweł |
author_facet | Gagat, Przemysław Bodył, Andrzej Mackiewicz, Paweł |
author_sort | Gagat, Przemysław |
collection | PubMed |
description | BACKGROUND: It is commonly assumed that a heterotrophic ancestor of the supergroup Archaeplastida/Plantae engulfed a cyanobacterium that was transformed into a primary plastid; however, it is still unclear how nuclear-encoded proteins initially were imported into the new organelle. Most proteins targeted to primary plastids carry a transit peptide and are transported post-translationally using Toc and Tic translocons. There are, however, several proteins with N-terminal signal peptides that are directed to higher plant plastids in vesicles derived from the endomembrane system (ES). The existence of these proteins inspired a hypothesis that all nuclear-encoded, plastid-targeted proteins initially carried signal peptides and were targeted to the ancestral primary plastid via the host ES. RESULTS: We present the first phylogenetic analyses of Arabidopsis thaliana α-carbonic anhydrase (CAH1), Oryza sativa nucleotide pyrophosphatase/phosphodiesterase (NPP1), and two O. sativa α-amylases (αAmy3, αAmy7), proteins that are directed to higher plant primary plastids via the ES. We also investigated protein disulfide isomerase (RB60) from the green alga Chlamydomonas reinhardtii because of its peculiar dual post- and co-translational targeting to both the plastid and ES. Our analyses show that these proteins all are of eukaryotic rather than cyanobacterial origin, and that their non-plastid homologs are equipped with signal peptides responsible for co-translational import into the host ES. Our results indicate that vesicular trafficking of proteins to primary plastids evolved long after the cyanobacterial endosymbiosis (possibly only in higher plants) to permit their glycosylation and/or transport to more than one cellular compartment. CONCLUSIONS: The proteins we analyzed are not relics of ES-mediated protein targeting to the ancestral primary plastid. Available data indicate that Toc- and Tic-based translocation dominated protein import into primary plastids from the beginning. Only a handful of host proteins, which already were targeted through the ES, later were adapted to reach the plastid via the vesicular trafficking. They represent a derived class of higher plant plastid-targeted proteins with an unusual evolutionary history. REVIEWERS: This article was reviewed by Prof. William Martin, Dr. Philippe Deschamps (nominated by Dr. Purificacion Lopez-Garcia) and Dr Simonetta Gribaldo. |
format | Online Article Text |
id | pubmed-3716720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37167202013-07-20 How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies Gagat, Przemysław Bodył, Andrzej Mackiewicz, Paweł Biol Direct Research BACKGROUND: It is commonly assumed that a heterotrophic ancestor of the supergroup Archaeplastida/Plantae engulfed a cyanobacterium that was transformed into a primary plastid; however, it is still unclear how nuclear-encoded proteins initially were imported into the new organelle. Most proteins targeted to primary plastids carry a transit peptide and are transported post-translationally using Toc and Tic translocons. There are, however, several proteins with N-terminal signal peptides that are directed to higher plant plastids in vesicles derived from the endomembrane system (ES). The existence of these proteins inspired a hypothesis that all nuclear-encoded, plastid-targeted proteins initially carried signal peptides and were targeted to the ancestral primary plastid via the host ES. RESULTS: We present the first phylogenetic analyses of Arabidopsis thaliana α-carbonic anhydrase (CAH1), Oryza sativa nucleotide pyrophosphatase/phosphodiesterase (NPP1), and two O. sativa α-amylases (αAmy3, αAmy7), proteins that are directed to higher plant primary plastids via the ES. We also investigated protein disulfide isomerase (RB60) from the green alga Chlamydomonas reinhardtii because of its peculiar dual post- and co-translational targeting to both the plastid and ES. Our analyses show that these proteins all are of eukaryotic rather than cyanobacterial origin, and that their non-plastid homologs are equipped with signal peptides responsible for co-translational import into the host ES. Our results indicate that vesicular trafficking of proteins to primary plastids evolved long after the cyanobacterial endosymbiosis (possibly only in higher plants) to permit their glycosylation and/or transport to more than one cellular compartment. CONCLUSIONS: The proteins we analyzed are not relics of ES-mediated protein targeting to the ancestral primary plastid. Available data indicate that Toc- and Tic-based translocation dominated protein import into primary plastids from the beginning. Only a handful of host proteins, which already were targeted through the ES, later were adapted to reach the plastid via the vesicular trafficking. They represent a derived class of higher plant plastid-targeted proteins with an unusual evolutionary history. REVIEWERS: This article was reviewed by Prof. William Martin, Dr. Philippe Deschamps (nominated by Dr. Purificacion Lopez-Garcia) and Dr Simonetta Gribaldo. BioMed Central 2013-07-11 /pmc/articles/PMC3716720/ /pubmed/23845039 http://dx.doi.org/10.1186/1745-6150-8-18 Text en Copyright © 2013 Gagat et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Gagat, Przemysław Bodył, Andrzej Mackiewicz, Paweł How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies |
title | How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies |
title_full | How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies |
title_fullStr | How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies |
title_full_unstemmed | How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies |
title_short | How protein targeting to primary plastids via the endomembrane system could have evolved? A new hypothesis based on phylogenetic studies |
title_sort | how protein targeting to primary plastids via the endomembrane system could have evolved? a new hypothesis based on phylogenetic studies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3716720/ https://www.ncbi.nlm.nih.gov/pubmed/23845039 http://dx.doi.org/10.1186/1745-6150-8-18 |
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