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Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat

Strigolactones (SLs) are a class of phytohormones regulating branching/tillering, and their biosynthesis has been associated with nutritional signals and plant adaptation to nutrient-limiting conditions. The enzymes in the SL biosynthetic pathway downstream of carlactone are of interest as they are...

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Autores principales: Sigalas, Petros P, Buchner, Peter, Thomas, Stephen G, Jamois, Frank, Arkoun, Mustapha, Yvin, Jean-Claude, Bennett, Malcolm J, Hawkesford, Malcolm J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049918/
https://www.ncbi.nlm.nih.gov/pubmed/36626359
http://dx.doi.org/10.1093/jxb/erad008
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author Sigalas, Petros P
Buchner, Peter
Thomas, Stephen G
Jamois, Frank
Arkoun, Mustapha
Yvin, Jean-Claude
Bennett, Malcolm J
Hawkesford, Malcolm J
author_facet Sigalas, Petros P
Buchner, Peter
Thomas, Stephen G
Jamois, Frank
Arkoun, Mustapha
Yvin, Jean-Claude
Bennett, Malcolm J
Hawkesford, Malcolm J
author_sort Sigalas, Petros P
collection PubMed
description Strigolactones (SLs) are a class of phytohormones regulating branching/tillering, and their biosynthesis has been associated with nutritional signals and plant adaptation to nutrient-limiting conditions. The enzymes in the SL biosynthetic pathway downstream of carlactone are of interest as they are responsible for structural diversity in SLs, particularly cytochrome P450 CYP711A subfamily members, such as MORE AXILLARY GROWTH1 (MAX1) in Arabidopsis. We identified 13 MAX1 homologues in wheat, clustering in four clades and five homoeologous subgroups. The utilization of RNA-sequencing data revealed a distinct expression pattern of MAX1 homologues in above- and below-ground tissues, providing insights into the distinct roles of MAX1 homologues in wheat. In addition, a transcriptional analysis showed that SL biosynthetic genes were systematically regulated by nitrogen supply. Nitrogen limitation led to larger transcriptional changes in the basal nodes than phosphorus limitation, which was consistent with the observed tillering suppression, as wheat showed higher sensitivity to nitrogen. The opposite was observed in roots, with phosphorus limitation leading to stronger induction of most SL biosynthetic genes compared with nitrogen limitation. The observed tissue-specific regulation of SL biosynthetic genes in response to nutritional signals is likely to reflect the dual role of SLs as rhizosphere signals and branching inhibitors.
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spelling pubmed-100499182023-03-30 Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat Sigalas, Petros P Buchner, Peter Thomas, Stephen G Jamois, Frank Arkoun, Mustapha Yvin, Jean-Claude Bennett, Malcolm J Hawkesford, Malcolm J J Exp Bot Research Papers Strigolactones (SLs) are a class of phytohormones regulating branching/tillering, and their biosynthesis has been associated with nutritional signals and plant adaptation to nutrient-limiting conditions. The enzymes in the SL biosynthetic pathway downstream of carlactone are of interest as they are responsible for structural diversity in SLs, particularly cytochrome P450 CYP711A subfamily members, such as MORE AXILLARY GROWTH1 (MAX1) in Arabidopsis. We identified 13 MAX1 homologues in wheat, clustering in four clades and five homoeologous subgroups. The utilization of RNA-sequencing data revealed a distinct expression pattern of MAX1 homologues in above- and below-ground tissues, providing insights into the distinct roles of MAX1 homologues in wheat. In addition, a transcriptional analysis showed that SL biosynthetic genes were systematically regulated by nitrogen supply. Nitrogen limitation led to larger transcriptional changes in the basal nodes than phosphorus limitation, which was consistent with the observed tillering suppression, as wheat showed higher sensitivity to nitrogen. The opposite was observed in roots, with phosphorus limitation leading to stronger induction of most SL biosynthetic genes compared with nitrogen limitation. The observed tissue-specific regulation of SL biosynthetic genes in response to nutritional signals is likely to reflect the dual role of SLs as rhizosphere signals and branching inhibitors. Oxford University Press 2023-01-10 /pmc/articles/PMC10049918/ /pubmed/36626359 http://dx.doi.org/10.1093/jxb/erad008 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 Papers
Sigalas, Petros P
Buchner, Peter
Thomas, Stephen G
Jamois, Frank
Arkoun, Mustapha
Yvin, Jean-Claude
Bennett, Malcolm J
Hawkesford, Malcolm J
Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat
title Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat
title_full Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat
title_fullStr Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat
title_full_unstemmed Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat
title_short Nutritional and tissue-specific regulation of cytochrome P450 CYP711A MAX1 homologues and strigolactone biosynthesis in wheat
title_sort nutritional and tissue-specific regulation of cytochrome p450 cyp711a max1 homologues and strigolactone biosynthesis in wheat
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049918/
https://www.ncbi.nlm.nih.gov/pubmed/36626359
http://dx.doi.org/10.1093/jxb/erad008
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