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cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development
Cell wall synthesis and protein glycosylation require the import of nucleotide diphosphate–sugar conjugates into the Golgi that must be counterbalanced by phosphate (Pi) export. Numerous Golgi nucleotide-sugar transporters have been characterized, but transporters mediating Golgi Pi export remain po...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231389/ https://www.ncbi.nlm.nih.gov/pubmed/36856724 http://dx.doi.org/10.1093/plphys/kiad123 |
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author | Hsieh, Yi-Fang Suslov, Dmitry Espen, Luca Schiavone, Marion Rautengarten, Carsten Griess-Osowski, Annika Voiniciuc, Catalin Poirier, Yves |
author_facet | Hsieh, Yi-Fang Suslov, Dmitry Espen, Luca Schiavone, Marion Rautengarten, Carsten Griess-Osowski, Annika Voiniciuc, Catalin Poirier, Yves |
author_sort | Hsieh, Yi-Fang |
collection | PubMed |
description | Cell wall synthesis and protein glycosylation require the import of nucleotide diphosphate–sugar conjugates into the Golgi that must be counterbalanced by phosphate (Pi) export. Numerous Golgi nucleotide-sugar transporters have been characterized, but transporters mediating Golgi Pi export remain poorly understood. We used plant and yeast genetics to characterize the role of 2 Arabidopsis (Arabidopsis thaliana) proteins possessing an EXS domain, namely ERD1A and ERD1B, in Golgi Pi homeostasis. ERD1A and ERD1B localized in cis-Golgi and were broadly expressed in vegetative and reproductive tissues. We identified ERD1 putative orthologs in algae, bryophytes, and vascular plants. Expressing ERD1A and ERD1B in yeast complemented the erd1 mutant phenotype of cellular Pi loss via exocytosis associated with reduced Golgi Pi export. The Arabidopsis erd1a mutant had a similar phenotype of apoplastic Pi loss dependent on exocytosis. ERD1A overexpression in Nicotiana benthamiana and Arabidopsis led to partial mislocalization of ERD1A to the plasma membrane and specific Pi export to the apoplastic space. Arabidopsis erd1a had defects in cell wall biosynthesis, which were associated with reduced shoot development, hypocotyl growth, cell wall extensibility, root elongation, pollen germination, pollen tube elongation, and fertility. We identified ERD1 proteins as Golgi Pi exporters that are essential for optimal plant growth and fertility. |
format | Online Article Text |
id | pubmed-10231389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102313892023-06-01 cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development Hsieh, Yi-Fang Suslov, Dmitry Espen, Luca Schiavone, Marion Rautengarten, Carsten Griess-Osowski, Annika Voiniciuc, Catalin Poirier, Yves Plant Physiol Research Article Cell wall synthesis and protein glycosylation require the import of nucleotide diphosphate–sugar conjugates into the Golgi that must be counterbalanced by phosphate (Pi) export. Numerous Golgi nucleotide-sugar transporters have been characterized, but transporters mediating Golgi Pi export remain poorly understood. We used plant and yeast genetics to characterize the role of 2 Arabidopsis (Arabidopsis thaliana) proteins possessing an EXS domain, namely ERD1A and ERD1B, in Golgi Pi homeostasis. ERD1A and ERD1B localized in cis-Golgi and were broadly expressed in vegetative and reproductive tissues. We identified ERD1 putative orthologs in algae, bryophytes, and vascular plants. Expressing ERD1A and ERD1B in yeast complemented the erd1 mutant phenotype of cellular Pi loss via exocytosis associated with reduced Golgi Pi export. The Arabidopsis erd1a mutant had a similar phenotype of apoplastic Pi loss dependent on exocytosis. ERD1A overexpression in Nicotiana benthamiana and Arabidopsis led to partial mislocalization of ERD1A to the plasma membrane and specific Pi export to the apoplastic space. Arabidopsis erd1a had defects in cell wall biosynthesis, which were associated with reduced shoot development, hypocotyl growth, cell wall extensibility, root elongation, pollen germination, pollen tube elongation, and fertility. We identified ERD1 proteins as Golgi Pi exporters that are essential for optimal plant growth and fertility. Oxford University Press 2023-02-28 /pmc/articles/PMC10231389/ /pubmed/36856724 http://dx.doi.org/10.1093/plphys/kiad123 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hsieh, Yi-Fang Suslov, Dmitry Espen, Luca Schiavone, Marion Rautengarten, Carsten Griess-Osowski, Annika Voiniciuc, Catalin Poirier, Yves cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development |
title |
cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development |
title_full |
cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development |
title_fullStr |
cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development |
title_full_unstemmed |
cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development |
title_short |
cis-Golgi phosphate transporters harboring an EXS domain are essential for plant growth and development |
title_sort | cis-golgi phosphate transporters harboring an exs domain are essential for plant growth and development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10231389/ https://www.ncbi.nlm.nih.gov/pubmed/36856724 http://dx.doi.org/10.1093/plphys/kiad123 |
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