Cargando…

Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism

BACKGROUND: Low availability of nitrogen (N) severely affects plant growth at different levels, which can be reverted by the resupply of N. To unravel the critical steps in primary metabolism underlying the growth adjustment in response to changes in N availability, transcriptomic and comprehensive...

Descripción completa

Detalles Bibliográficos
Autores principales: Fataftah, Nazeer, Mohr, Christina, Hajirezaei, Mohammad-Reza, Wirén, Nicolaus von, Humbeck, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935972/
https://www.ncbi.nlm.nih.gov/pubmed/29728053
http://dx.doi.org/10.1186/s12870-018-1301-x
_version_ 1783320367145680896
author Fataftah, Nazeer
Mohr, Christina
Hajirezaei, Mohammad-Reza
Wirén, Nicolaus von
Humbeck, Klaus
author_facet Fataftah, Nazeer
Mohr, Christina
Hajirezaei, Mohammad-Reza
Wirén, Nicolaus von
Humbeck, Klaus
author_sort Fataftah, Nazeer
collection PubMed
description BACKGROUND: Low availability of nitrogen (N) severely affects plant growth at different levels, which can be reverted by the resupply of N. To unravel the critical steps in primary metabolism underlying the growth adjustment in response to changes in N availability, transcriptomic and comprehensive metabolite analyses were performed in barley using primary leaves at early and later stages of N deprivation, and after N resupply to N-deficient plants. RESULT: N deficiency in leaves caused differential regulation of 1947 genes, mostly belonging to the functional classes photosynthesis, cell wall degradation, lipid degradation, amino acid degradation, transcription factors, phytohormone metabolism and receptor-like kinases. Interestingly, 62% of the genes responding to low N were regulated in the opposite direction after two days of N resupply. Reprogramming of gene transcription was linked to metabolic rearrangements and affected the metabolism of amino acids and sugars. The levels of major amino acids, including Glu, Asp, Ser, Gln, Gly, Thr, Ala, and Val, decreased during primary leaf age and, more pronounced, during low N-induced senescence, which was efficiently reverted after resupply of N. A significant decrease was observed for pyruvate and metabolites involved in the TCA cycle under low N, and this was reverted to initial levels after 5 days of N resupply. Correspondingly, transcript levels of genes coding for pyruvate kinase, pyruvate dehydrogenase, and pyruvate orthophosphate dikinase followed the same trend as related metabolites. CONCLUSION: Our results show that upon N limitation a specific pathway for remobilization at the link between glycolysis and TCA cycle in barley is established that is at least partly regulated by a strict reprogramming of the gene coding for pyruvate orthophosphate dikinase. Further analysis of this pathway, its regulatory levels and biochemical changing of pyruvate metabolism enzymes in response to N availability is needed to determine the link between N status and primary metabolism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1301-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5935972
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-59359722018-05-11 Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism Fataftah, Nazeer Mohr, Christina Hajirezaei, Mohammad-Reza Wirén, Nicolaus von Humbeck, Klaus BMC Plant Biol Research Article BACKGROUND: Low availability of nitrogen (N) severely affects plant growth at different levels, which can be reverted by the resupply of N. To unravel the critical steps in primary metabolism underlying the growth adjustment in response to changes in N availability, transcriptomic and comprehensive metabolite analyses were performed in barley using primary leaves at early and later stages of N deprivation, and after N resupply to N-deficient plants. RESULT: N deficiency in leaves caused differential regulation of 1947 genes, mostly belonging to the functional classes photosynthesis, cell wall degradation, lipid degradation, amino acid degradation, transcription factors, phytohormone metabolism and receptor-like kinases. Interestingly, 62% of the genes responding to low N were regulated in the opposite direction after two days of N resupply. Reprogramming of gene transcription was linked to metabolic rearrangements and affected the metabolism of amino acids and sugars. The levels of major amino acids, including Glu, Asp, Ser, Gln, Gly, Thr, Ala, and Val, decreased during primary leaf age and, more pronounced, during low N-induced senescence, which was efficiently reverted after resupply of N. A significant decrease was observed for pyruvate and metabolites involved in the TCA cycle under low N, and this was reverted to initial levels after 5 days of N resupply. Correspondingly, transcript levels of genes coding for pyruvate kinase, pyruvate dehydrogenase, and pyruvate orthophosphate dikinase followed the same trend as related metabolites. CONCLUSION: Our results show that upon N limitation a specific pathway for remobilization at the link between glycolysis and TCA cycle in barley is established that is at least partly regulated by a strict reprogramming of the gene coding for pyruvate orthophosphate dikinase. Further analysis of this pathway, its regulatory levels and biochemical changing of pyruvate metabolism enzymes in response to N availability is needed to determine the link between N status and primary metabolism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1301-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-04 /pmc/articles/PMC5935972/ /pubmed/29728053 http://dx.doi.org/10.1186/s12870-018-1301-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Fataftah, Nazeer
Mohr, Christina
Hajirezaei, Mohammad-Reza
Wirén, Nicolaus von
Humbeck, Klaus
Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
title Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
title_full Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
title_fullStr Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
title_full_unstemmed Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
title_short Changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
title_sort changes in nitrogen availability lead to a reprogramming of pyruvate metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935972/
https://www.ncbi.nlm.nih.gov/pubmed/29728053
http://dx.doi.org/10.1186/s12870-018-1301-x
work_keys_str_mv AT fataftahnazeer changesinnitrogenavailabilityleadtoareprogrammingofpyruvatemetabolism
AT mohrchristina changesinnitrogenavailabilityleadtoareprogrammingofpyruvatemetabolism
AT hajirezaeimohammadreza changesinnitrogenavailabilityleadtoareprogrammingofpyruvatemetabolism
AT wirennicolausvon changesinnitrogenavailabilityleadtoareprogrammingofpyruvatemetabolism
AT humbeckklaus changesinnitrogenavailabilityleadtoareprogrammingofpyruvatemetabolism