Cargando…

Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana

In this study, evidence is provided for the role of fructose-1,6-bisphosphatases (FBPases) in plant development and carbohydrate synthesis and distribution by analysing two Arabidopsis thaliana T-DNA knockout mutant lines, cyfbp and cfbp1, and one double mutant cyfbp cfbp1 which affect each FBPase i...

Descripción completa

Detalles Bibliográficos
Autores principales: Rojas-González, José A., Soto-Súarez, Mauricio, García-Díaz, Ángel, Romero-Puertas, María C., Sandalio, Luisa M., Mérida, Ángel, Thormählen, Ina, Geigenberger, Peter, Serrato, Antonio J., Sahrawy, Mariam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986871/
https://www.ncbi.nlm.nih.gov/pubmed/25743161
http://dx.doi.org/10.1093/jxb/erv062
_version_ 1782448231601405952
author Rojas-González, José A.
Soto-Súarez, Mauricio
García-Díaz, Ángel
Romero-Puertas, María C.
Sandalio, Luisa M.
Mérida, Ángel
Thormählen, Ina
Geigenberger, Peter
Serrato, Antonio J.
Sahrawy, Mariam
author_facet Rojas-González, José A.
Soto-Súarez, Mauricio
García-Díaz, Ángel
Romero-Puertas, María C.
Sandalio, Luisa M.
Mérida, Ángel
Thormählen, Ina
Geigenberger, Peter
Serrato, Antonio J.
Sahrawy, Mariam
author_sort Rojas-González, José A.
collection PubMed
description In this study, evidence is provided for the role of fructose-1,6-bisphosphatases (FBPases) in plant development and carbohydrate synthesis and distribution by analysing two Arabidopsis thaliana T-DNA knockout mutant lines, cyfbp and cfbp1, and one double mutant cyfbp cfbp1 which affect each FBPase isoform, cytosolic and chloroplastic, respectively. cyFBP is involved in sucrose synthesis, whilst cFBP1 is a key enzyme in the Calvin–Benson cycle. In addition to the smaller rosette size and lower rate of photosynthesis, the lack of cFBP1 in the mutants cfbp1 and cyfbp cfbp1 leads to a lower content of soluble sugars, less starch accumulation, and a greater superoxide dismutase (SOD) activity. The mutants also had some developmental alterations, including stomatal opening defects and increased numbers of root vascular layers. Complementation also confirmed that the mutant phenotypes were caused by disruption of the cFBP1 gene. cyfbp mutant plants without cyFBP showed a higher starch content in the chloroplasts, but this did not greatly affect the phenotype. Notably, the sucrose content in cyfbp was close to that found in the wild type. The cyfbp cfbp1 double mutant displayed features of both parental lines but had the cfbp1 phenotype. All the mutants accumulated fructose-1,6-bisphosphate and triose-phosphate during the light period. These results prove that while the lack of cFBP1 induces important changes in a wide range of metabolites such as amino acids, sugars, and organic acids, the lack of cyFBP activity in Arabidopsis essentially provokes a carbon metabolism imbalance which does not compromise the viability of the double mutant cyfbp cfbp1.
format Online
Article
Text
id pubmed-4986871
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-49868712016-08-22 Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana Rojas-González, José A. Soto-Súarez, Mauricio García-Díaz, Ángel Romero-Puertas, María C. Sandalio, Luisa M. Mérida, Ángel Thormählen, Ina Geigenberger, Peter Serrato, Antonio J. Sahrawy, Mariam J Exp Bot Research Paper In this study, evidence is provided for the role of fructose-1,6-bisphosphatases (FBPases) in plant development and carbohydrate synthesis and distribution by analysing two Arabidopsis thaliana T-DNA knockout mutant lines, cyfbp and cfbp1, and one double mutant cyfbp cfbp1 which affect each FBPase isoform, cytosolic and chloroplastic, respectively. cyFBP is involved in sucrose synthesis, whilst cFBP1 is a key enzyme in the Calvin–Benson cycle. In addition to the smaller rosette size and lower rate of photosynthesis, the lack of cFBP1 in the mutants cfbp1 and cyfbp cfbp1 leads to a lower content of soluble sugars, less starch accumulation, and a greater superoxide dismutase (SOD) activity. The mutants also had some developmental alterations, including stomatal opening defects and increased numbers of root vascular layers. Complementation also confirmed that the mutant phenotypes were caused by disruption of the cFBP1 gene. cyfbp mutant plants without cyFBP showed a higher starch content in the chloroplasts, but this did not greatly affect the phenotype. Notably, the sucrose content in cyfbp was close to that found in the wild type. The cyfbp cfbp1 double mutant displayed features of both parental lines but had the cfbp1 phenotype. All the mutants accumulated fructose-1,6-bisphosphate and triose-phosphate during the light period. These results prove that while the lack of cFBP1 induces important changes in a wide range of metabolites such as amino acids, sugars, and organic acids, the lack of cyFBP activity in Arabidopsis essentially provokes a carbon metabolism imbalance which does not compromise the viability of the double mutant cyfbp cfbp1. Oxford University Press 2015-05 2015-03-05 /pmc/articles/PMC4986871/ /pubmed/25743161 http://dx.doi.org/10.1093/jxb/erv062 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Rojas-González, José A.
Soto-Súarez, Mauricio
García-Díaz, Ángel
Romero-Puertas, María C.
Sandalio, Luisa M.
Mérida, Ángel
Thormählen, Ina
Geigenberger, Peter
Serrato, Antonio J.
Sahrawy, Mariam
Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana
title Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana
title_full Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana
title_fullStr Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana
title_full_unstemmed Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana
title_short Disruption of both chloroplastic and cytosolic FBPase genes results in a dwarf phenotype and important starch and metabolite changes in Arabidopsis thaliana
title_sort disruption of both chloroplastic and cytosolic fbpase genes results in a dwarf phenotype and important starch and metabolite changes in arabidopsis thaliana
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986871/
https://www.ncbi.nlm.nih.gov/pubmed/25743161
http://dx.doi.org/10.1093/jxb/erv062
work_keys_str_mv AT rojasgonzalezjosea disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT sotosuarezmauricio disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT garciadiazangel disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT romeropuertasmariac disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT sandalioluisam disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT meridaangel disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT thormahlenina disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT geigenbergerpeter disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT serratoantonioj disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana
AT sahrawymariam disruptionofbothchloroplasticandcytosolicfbpasegenesresultsinadwarfphenotypeandimportantstarchandmetabolitechangesinarabidopsisthaliana