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The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)

Plant PHO1 proteins play a central role in the translocation and sensing of inorganic phosphate. The maize ( Zea mays ssp. mays ) genome encodes two co‐orthologs of the Arabidopsis PHO1 gene, designated ZmPho1;2a and ZmPho1;2b. Here, we report the characterization of the transposon footprint allele...

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Autores principales: Alonso‐Nieves, Ana Laura, Salazar‐Vidal, M. Nancy, Torres‐Rodríguez, J. Vladimir, Pérez‐Vázquez, Leonardo M., Massange‐Sánchez, Julio A., Gillmor, C. Stewart, Sawers, Ruairidh J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277030/
https://www.ncbi.nlm.nih.gov/pubmed/35844781
http://dx.doi.org/10.1002/pld3.416
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author Alonso‐Nieves, Ana Laura
Salazar‐Vidal, M. Nancy
Torres‐Rodríguez, J. Vladimir
Pérez‐Vázquez, Leonardo M.
Massange‐Sánchez, Julio A.
Gillmor, C. Stewart
Sawers, Ruairidh J. H.
author_facet Alonso‐Nieves, Ana Laura
Salazar‐Vidal, M. Nancy
Torres‐Rodríguez, J. Vladimir
Pérez‐Vázquez, Leonardo M.
Massange‐Sánchez, Julio A.
Gillmor, C. Stewart
Sawers, Ruairidh J. H.
author_sort Alonso‐Nieves, Ana Laura
collection PubMed
description Plant PHO1 proteins play a central role in the translocation and sensing of inorganic phosphate. The maize ( Zea mays ssp. mays ) genome encodes two co‐orthologs of the Arabidopsis PHO1 gene, designated ZmPho1;2a and ZmPho1;2b. Here, we report the characterization of the transposon footprint allele Zmpho1;2a′‐m1.1, which we refer to hereafter as pho1;2a. The pho1;2a allele is a stable derivative formed by excision of an Activator transposable element from the ZmPho1;2a gene. The pho1;2a allele contains an 8‐bp insertion at the point of transposon excision that disrupts the reading frame and is predicted to generate a premature translational stop. We show that the pho1;2a allele is linked to a dosage‐dependent reduction in Pho1;2a transcript accumulation and a mild reduction in seedling growth. Characterization of shoot and root transcriptomes under full nutrient, low nitrogen, low phosphorus, and combined low nitrogen and low phosphorus conditions identified 1100 differentially expressed genes between wild‐type plants and plants carrying the pho1;2a mutation. Of these 1100 genes, 966 were upregulated in plants carrying pho1;2a, indicating the wild‐type PHO1;2a to predominantly impact negative gene regulation. Gene set enrichment analysis of the pho1;2a‐misregulated genes revealed associations with phytohormone signaling and the phosphate starvation response. In roots, differential expression was broadly consistent across all nutrient conditions. In leaves, differential expression was largely specific to low phosphorus and combined low nitrogen and low phosphorus conditions. Of 276 genes upregulated in the leaves of pho1;2a mutants in the low phosphorus condition, 153 were themselves induced in wild‐type plants with respect to the full nutrient condition. Our observations suggest that Pho1;2a functions in the fine‐tuning of the transcriptional response to phosphate starvation through maintenance and/or sensing of plant phosphate status.
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spelling pubmed-92770302022-07-15 The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.) Alonso‐Nieves, Ana Laura Salazar‐Vidal, M. Nancy Torres‐Rodríguez, J. Vladimir Pérez‐Vázquez, Leonardo M. Massange‐Sánchez, Julio A. Gillmor, C. Stewart Sawers, Ruairidh J. H. Plant Direct Original Research Plant PHO1 proteins play a central role in the translocation and sensing of inorganic phosphate. The maize ( Zea mays ssp. mays ) genome encodes two co‐orthologs of the Arabidopsis PHO1 gene, designated ZmPho1;2a and ZmPho1;2b. Here, we report the characterization of the transposon footprint allele Zmpho1;2a′‐m1.1, which we refer to hereafter as pho1;2a. The pho1;2a allele is a stable derivative formed by excision of an Activator transposable element from the ZmPho1;2a gene. The pho1;2a allele contains an 8‐bp insertion at the point of transposon excision that disrupts the reading frame and is predicted to generate a premature translational stop. We show that the pho1;2a allele is linked to a dosage‐dependent reduction in Pho1;2a transcript accumulation and a mild reduction in seedling growth. Characterization of shoot and root transcriptomes under full nutrient, low nitrogen, low phosphorus, and combined low nitrogen and low phosphorus conditions identified 1100 differentially expressed genes between wild‐type plants and plants carrying the pho1;2a mutation. Of these 1100 genes, 966 were upregulated in plants carrying pho1;2a, indicating the wild‐type PHO1;2a to predominantly impact negative gene regulation. Gene set enrichment analysis of the pho1;2a‐misregulated genes revealed associations with phytohormone signaling and the phosphate starvation response. In roots, differential expression was broadly consistent across all nutrient conditions. In leaves, differential expression was largely specific to low phosphorus and combined low nitrogen and low phosphorus conditions. Of 276 genes upregulated in the leaves of pho1;2a mutants in the low phosphorus condition, 153 were themselves induced in wild‐type plants with respect to the full nutrient condition. Our observations suggest that Pho1;2a functions in the fine‐tuning of the transcriptional response to phosphate starvation through maintenance and/or sensing of plant phosphate status. John Wiley and Sons Inc. 2022-07-12 /pmc/articles/PMC9277030/ /pubmed/35844781 http://dx.doi.org/10.1002/pld3.416 Text en © 2022 The Authors. Plant Direct published by American Society of Plant Biologists and the Society for Experimental Biology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Alonso‐Nieves, Ana Laura
Salazar‐Vidal, M. Nancy
Torres‐Rodríguez, J. Vladimir
Pérez‐Vázquez, Leonardo M.
Massange‐Sánchez, Julio A.
Gillmor, C. Stewart
Sawers, Ruairidh J. H.
The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)
title The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)
title_full The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)
title_fullStr The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)
title_full_unstemmed The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)
title_short The pho1;2a′‐m1.1 allele of Phosphate1 conditions misregulation of the phosphorus starvation response in maize ( Zea mays ssp. mays L.)
title_sort pho1;2a′‐m1.1 allele of phosphate1 conditions misregulation of the phosphorus starvation response in maize ( zea mays ssp. mays l.)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277030/
https://www.ncbi.nlm.nih.gov/pubmed/35844781
http://dx.doi.org/10.1002/pld3.416
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