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CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth
Lateral root (LR) proliferation is a major determinant of soil nutrient uptake. How resource allocation controls the extent of LR growth remains unresolved. We used genetic, physiological, transcriptomic, and grafting approaches to define a role for C-TERMINALLY ENCODED PEPTIDE RECEPTOR 1 (CEPR1) in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685651/ https://www.ncbi.nlm.nih.gov/pubmed/31056646 http://dx.doi.org/10.1093/jxb/erz207 |
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author | Chapman, Kelly Taleski, Michael Ogilvie, Huw A Imin, Nijat Djordjevic, Michael A |
author_facet | Chapman, Kelly Taleski, Michael Ogilvie, Huw A Imin, Nijat Djordjevic, Michael A |
author_sort | Chapman, Kelly |
collection | PubMed |
description | Lateral root (LR) proliferation is a major determinant of soil nutrient uptake. How resource allocation controls the extent of LR growth remains unresolved. We used genetic, physiological, transcriptomic, and grafting approaches to define a role for C-TERMINALLY ENCODED PEPTIDE RECEPTOR 1 (CEPR1) in controlling sucrose-dependent LR growth. CEPR1 inhibited LR growth in response to applied sucrose, other metabolizable sugars, and elevated light intensity. Pathways through CEPR1 restricted LR growth by reducing LR meristem size and the length of mature LR cells. RNA-sequencing of wild-type (WT) and cepr1-1 roots with or without sucrose treatment revealed an intersection of CEP–CEPR1 signalling with the sucrose transcriptional response. Sucrose up-regulated several CEP genes, supporting a specific role for CEP–CEPR1 in the response to sucrose. Moreover, genes with basally perturbed expression in cepr1-1 overlap with WT sucrose-responsive genes significantly. We found that exogenous CEP inhibited LR growth via CEPR1 by reducing LR meristem size and mature cell length. This result is consistent with CEP–CEPR1 acting to curtail the extent of sucrose-dependent LR growth. Reciprocal grafting indicates that LR growth inhibition requires CEPR1 in both the roots and shoots. Our results reveal a new role for CEP–CEPR1 signalling in controlling LR growth in response to sucrose. |
format | Online Article Text |
id | pubmed-6685651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66856512019-08-12 CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth Chapman, Kelly Taleski, Michael Ogilvie, Huw A Imin, Nijat Djordjevic, Michael A J Exp Bot Research Papers Lateral root (LR) proliferation is a major determinant of soil nutrient uptake. How resource allocation controls the extent of LR growth remains unresolved. We used genetic, physiological, transcriptomic, and grafting approaches to define a role for C-TERMINALLY ENCODED PEPTIDE RECEPTOR 1 (CEPR1) in controlling sucrose-dependent LR growth. CEPR1 inhibited LR growth in response to applied sucrose, other metabolizable sugars, and elevated light intensity. Pathways through CEPR1 restricted LR growth by reducing LR meristem size and the length of mature LR cells. RNA-sequencing of wild-type (WT) and cepr1-1 roots with or without sucrose treatment revealed an intersection of CEP–CEPR1 signalling with the sucrose transcriptional response. Sucrose up-regulated several CEP genes, supporting a specific role for CEP–CEPR1 in the response to sucrose. Moreover, genes with basally perturbed expression in cepr1-1 overlap with WT sucrose-responsive genes significantly. We found that exogenous CEP inhibited LR growth via CEPR1 by reducing LR meristem size and mature cell length. This result is consistent with CEP–CEPR1 acting to curtail the extent of sucrose-dependent LR growth. Reciprocal grafting indicates that LR growth inhibition requires CEPR1 in both the roots and shoots. Our results reveal a new role for CEP–CEPR1 signalling in controlling LR growth in response to sucrose. Oxford University Press 2019-08-01 2019-05-06 /pmc/articles/PMC6685651/ /pubmed/31056646 http://dx.doi.org/10.1093/jxb/erz207 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Papers Chapman, Kelly Taleski, Michael Ogilvie, Huw A Imin, Nijat Djordjevic, Michael A CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
title |
CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
title_full |
CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
title_fullStr |
CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
title_full_unstemmed |
CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
title_short |
CEP–CEPR1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
title_sort | cep–cepr1 signalling inhibits the sucrose-dependent enhancement of lateral root growth |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685651/ https://www.ncbi.nlm.nih.gov/pubmed/31056646 http://dx.doi.org/10.1093/jxb/erz207 |
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