Cargando…

MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula

BACKGROUND: Legumes have the unique capability to undergo root nodule and arbuscular mycorrhizal symbiosis. Both types of root endosymbiosis are regulated by NSP2, which is a target of microRNA171h (miR171h). Although, recent data implies that miR171h specifically restricts arbuscular mycorrhizal sy...

Descripción completa

Detalles Bibliográficos
Autores principales: Hofferek, Vinzenz, Mendrinna, Amelie, Gaude, Nicole, Krajinski, Franziska, Devers, Emanuel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115173/
https://www.ncbi.nlm.nih.gov/pubmed/25928247
http://dx.doi.org/10.1186/s12870-014-0199-1
_version_ 1782328515251666944
author Hofferek, Vinzenz
Mendrinna, Amelie
Gaude, Nicole
Krajinski, Franziska
Devers, Emanuel A
author_facet Hofferek, Vinzenz
Mendrinna, Amelie
Gaude, Nicole
Krajinski, Franziska
Devers, Emanuel A
author_sort Hofferek, Vinzenz
collection PubMed
description BACKGROUND: Legumes have the unique capability to undergo root nodule and arbuscular mycorrhizal symbiosis. Both types of root endosymbiosis are regulated by NSP2, which is a target of microRNA171h (miR171h). Although, recent data implies that miR171h specifically restricts arbuscular mycorrhizal symbiosis in the root elongation zone of Medicago truncatula roots, there is limited knowledge available about the spatio-temporal regulation of miR171h expression at different physiological and symbiotic conditions. RESULTS: We show that miR171h is functionally expressed from an unusual long primary transcript, previously predicted to encode two identical miR171h strands. Both miR171h and NSP2 transcripts display a complex regulation pattern, which involves the symbiotic status and the fertilization regime of the plant. Quantitative Real-time PCR revealed that miR171h and NSP2 transcript levels show a clear anti-correlation in all tested conditions except in mycorrhizal roots, where NSP2 transcript levels were induced despite of an increased miR171h expression. This was also supported by a clear correlation of transcript levels of NSP2 and MtPt4, a phosphate transporter specifically expressed in a functional AM symbiosis. MiR171h is strongly induced in plants growing in sufficient phosphate conditions, which we demonstrate to be independent of the CRE1 signaling pathway and which is also not required for transcriptional induction of NSP2 in mycorrhizal roots. In situ hybridization and promoter activity analysis of both genes confirmed the complex regulation involving the symbiotic status, P and N nutrition, where both genes show a mainly mutual exclusive expression pattern. Overexpression of miR171h in M. truncatula roots led to a reduction in mycorrhizal colonization and to a reduced nodulation by Sinorhizobium meliloti. CONCLUSION: The spatio-temporal expression of miR171h and NSP2 is tightly linked to the nutritional status of the plant and, together with the results from the overexpression analysis, points to an important function of miR171h to integrate the nutrient homeostasis in order to safeguard the expression domain of NSP2 during both, arbuscular mycorrhizal and root nodule symbiosis.
format Online
Article
Text
id pubmed-4115173
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-41151732014-07-31 MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula Hofferek, Vinzenz Mendrinna, Amelie Gaude, Nicole Krajinski, Franziska Devers, Emanuel A BMC Plant Biol Research Article BACKGROUND: Legumes have the unique capability to undergo root nodule and arbuscular mycorrhizal symbiosis. Both types of root endosymbiosis are regulated by NSP2, which is a target of microRNA171h (miR171h). Although, recent data implies that miR171h specifically restricts arbuscular mycorrhizal symbiosis in the root elongation zone of Medicago truncatula roots, there is limited knowledge available about the spatio-temporal regulation of miR171h expression at different physiological and symbiotic conditions. RESULTS: We show that miR171h is functionally expressed from an unusual long primary transcript, previously predicted to encode two identical miR171h strands. Both miR171h and NSP2 transcripts display a complex regulation pattern, which involves the symbiotic status and the fertilization regime of the plant. Quantitative Real-time PCR revealed that miR171h and NSP2 transcript levels show a clear anti-correlation in all tested conditions except in mycorrhizal roots, where NSP2 transcript levels were induced despite of an increased miR171h expression. This was also supported by a clear correlation of transcript levels of NSP2 and MtPt4, a phosphate transporter specifically expressed in a functional AM symbiosis. MiR171h is strongly induced in plants growing in sufficient phosphate conditions, which we demonstrate to be independent of the CRE1 signaling pathway and which is also not required for transcriptional induction of NSP2 in mycorrhizal roots. In situ hybridization and promoter activity analysis of both genes confirmed the complex regulation involving the symbiotic status, P and N nutrition, where both genes show a mainly mutual exclusive expression pattern. Overexpression of miR171h in M. truncatula roots led to a reduction in mycorrhizal colonization and to a reduced nodulation by Sinorhizobium meliloti. CONCLUSION: The spatio-temporal expression of miR171h and NSP2 is tightly linked to the nutritional status of the plant and, together with the results from the overexpression analysis, points to an important function of miR171h to integrate the nutrient homeostasis in order to safeguard the expression domain of NSP2 during both, arbuscular mycorrhizal and root nodule symbiosis. BioMed Central 2014-07-23 /pmc/articles/PMC4115173/ /pubmed/25928247 http://dx.doi.org/10.1186/s12870-014-0199-1 Text en Copyright © 2014 Hofferek et al. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hofferek, Vinzenz
Mendrinna, Amelie
Gaude, Nicole
Krajinski, Franziska
Devers, Emanuel A
MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula
title MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula
title_full MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula
title_fullStr MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula
title_full_unstemmed MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula
title_short MiR171h restricts root symbioses and shows like its target NSP2 a complex transcriptional regulation in Medicago truncatula
title_sort mir171h restricts root symbioses and shows like its target nsp2 a complex transcriptional regulation in medicago truncatula
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115173/
https://www.ncbi.nlm.nih.gov/pubmed/25928247
http://dx.doi.org/10.1186/s12870-014-0199-1
work_keys_str_mv AT hofferekvinzenz mir171hrestrictsrootsymbiosesandshowslikeitstargetnsp2acomplextranscriptionalregulationinmedicagotruncatula
AT mendrinnaamelie mir171hrestrictsrootsymbiosesandshowslikeitstargetnsp2acomplextranscriptionalregulationinmedicagotruncatula
AT gaudenicole mir171hrestrictsrootsymbiosesandshowslikeitstargetnsp2acomplextranscriptionalregulationinmedicagotruncatula
AT krajinskifranziska mir171hrestrictsrootsymbiosesandshowslikeitstargetnsp2acomplextranscriptionalregulationinmedicagotruncatula
AT deversemanuela mir171hrestrictsrootsymbiosesandshowslikeitstargetnsp2acomplextranscriptionalregulationinmedicagotruncatula