Cargando…

Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana

The cytosolic level of inorganic pyrophosphate (PPi) is finely regulated, with PPi hydrolyzed primarily by the vacuolar H(+)-pyrophosphatase (H(+)-PPase, VHP1/FUGU5/AVP1) and secondarily by five cytosolic soluble pyrophosphatases (sPPases; PPa1–PPa5) in Arabidopsis thaliana. Loss-of-function mutants...

Descripción completa

Detalles Bibliográficos
Autores principales: Fukuda, Mayu, Mieda, Marika, Sato, Ryosuke, Kinoshita, Satoru, Tomoyama, Takaaki, Ferjani, Ali, Maeshima, Masayoshi, Segami, Shoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266078/
https://www.ncbi.nlm.nih.gov/pubmed/32528505
http://dx.doi.org/10.3389/fpls.2020.00655
_version_ 1783541240690638848
author Fukuda, Mayu
Mieda, Marika
Sato, Ryosuke
Kinoshita, Satoru
Tomoyama, Takaaki
Ferjani, Ali
Maeshima, Masayoshi
Segami, Shoji
author_facet Fukuda, Mayu
Mieda, Marika
Sato, Ryosuke
Kinoshita, Satoru
Tomoyama, Takaaki
Ferjani, Ali
Maeshima, Masayoshi
Segami, Shoji
author_sort Fukuda, Mayu
collection PubMed
description The cytosolic level of inorganic pyrophosphate (PPi) is finely regulated, with PPi hydrolyzed primarily by the vacuolar H(+)-pyrophosphatase (H(+)-PPase, VHP1/FUGU5/AVP1) and secondarily by five cytosolic soluble pyrophosphatases (sPPases; PPa1–PPa5) in Arabidopsis thaliana. Loss-of-function mutants of H(+)-PPase (fugu5s) have been reported to show atrophic phenotypes in their rosette leaves when nitrate is the sole nitrogen source in the culture medium. For this phenotype, two questions remain unanswered: why does atrophy depend on physical contact between shoots and the medium, and how does ammonium prevent such atrophy. To understand the mechanism driving this phenotype, we analyzed the growth and phenotypes of mutants on ammonium-free medium in detail. fugu5-1 showed cuticle defects, cell swelling, reduced β-glucan levels, and vein malformation in the leaves, suggesting cell wall weakening and cell lethality. Based on the observation in the double mutants fugu5-1 ppa1 and fugu5-1 ppa4 of more severe atrophy compared to fugu5-1, the nitrogen-dependent phenotype might be linked to PPi metabolism. To elucidate the role of ammonium in this process, we examined the fluctuations of sPPase mRNA levels and the possibility of alternative PPi-removing factors, such as other types of pyrophosphatase. First, we found that both the protein and mRNA levels of sPPases were unaffected by the nitrogen source. Second, to assess the influence of other PPi-removing factors, we examined the phenotypes of triple knockout mutants of H(+)-PPase and two sPPases on ammonium-containing medium. Both fugu5 ppa1 ppa2 and fugu5 ppa1 ppa4 had nearly lethal embryonic phenotypes, with the survivors showing striking dwarfism and abnormal morphology. Moreover, fugu5 ppa1(+/–) ppa4 showed severe atrophy at the leaf margins. The other triple mutants, fugu5 ppa1 ppa5 and fugu5 ppa2 ppa4, exhibited death of root hairs and were nearly sterile due to deformed pistils, respectively, even when grown on standard medium. Together, these results suggest that H(+)-PPase and sPPases act in concert to maintain PPi homeostasis, that the existence of other PPi removers is unlikely, and that ammonium may suppress the production of PPi during nitrogen metabolism rather than stimulating PPi hydrolysis.
format Online
Article
Text
id pubmed-7266078
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-72660782020-06-10 Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana Fukuda, Mayu Mieda, Marika Sato, Ryosuke Kinoshita, Satoru Tomoyama, Takaaki Ferjani, Ali Maeshima, Masayoshi Segami, Shoji Front Plant Sci Plant Science The cytosolic level of inorganic pyrophosphate (PPi) is finely regulated, with PPi hydrolyzed primarily by the vacuolar H(+)-pyrophosphatase (H(+)-PPase, VHP1/FUGU5/AVP1) and secondarily by five cytosolic soluble pyrophosphatases (sPPases; PPa1–PPa5) in Arabidopsis thaliana. Loss-of-function mutants of H(+)-PPase (fugu5s) have been reported to show atrophic phenotypes in their rosette leaves when nitrate is the sole nitrogen source in the culture medium. For this phenotype, two questions remain unanswered: why does atrophy depend on physical contact between shoots and the medium, and how does ammonium prevent such atrophy. To understand the mechanism driving this phenotype, we analyzed the growth and phenotypes of mutants on ammonium-free medium in detail. fugu5-1 showed cuticle defects, cell swelling, reduced β-glucan levels, and vein malformation in the leaves, suggesting cell wall weakening and cell lethality. Based on the observation in the double mutants fugu5-1 ppa1 and fugu5-1 ppa4 of more severe atrophy compared to fugu5-1, the nitrogen-dependent phenotype might be linked to PPi metabolism. To elucidate the role of ammonium in this process, we examined the fluctuations of sPPase mRNA levels and the possibility of alternative PPi-removing factors, such as other types of pyrophosphatase. First, we found that both the protein and mRNA levels of sPPases were unaffected by the nitrogen source. Second, to assess the influence of other PPi-removing factors, we examined the phenotypes of triple knockout mutants of H(+)-PPase and two sPPases on ammonium-containing medium. Both fugu5 ppa1 ppa2 and fugu5 ppa1 ppa4 had nearly lethal embryonic phenotypes, with the survivors showing striking dwarfism and abnormal morphology. Moreover, fugu5 ppa1(+/–) ppa4 showed severe atrophy at the leaf margins. The other triple mutants, fugu5 ppa1 ppa5 and fugu5 ppa2 ppa4, exhibited death of root hairs and were nearly sterile due to deformed pistils, respectively, even when grown on standard medium. Together, these results suggest that H(+)-PPase and sPPases act in concert to maintain PPi homeostasis, that the existence of other PPi removers is unlikely, and that ammonium may suppress the production of PPi during nitrogen metabolism rather than stimulating PPi hydrolysis. Frontiers Media S.A. 2020-05-26 /pmc/articles/PMC7266078/ /pubmed/32528505 http://dx.doi.org/10.3389/fpls.2020.00655 Text en Copyright © 2020 Fukuda, Mieda, Sato, Kinoshita, Tomoyama, Ferjani, Maeshima and Segami. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Fukuda, Mayu
Mieda, Marika
Sato, Ryosuke
Kinoshita, Satoru
Tomoyama, Takaaki
Ferjani, Ali
Maeshima, Masayoshi
Segami, Shoji
Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana
title Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana
title_full Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana
title_fullStr Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana
title_full_unstemmed Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana
title_short Lack of Vacuolar H(+) -Pyrophosphatase and Cytosolic Pyrophosphatases Causes Fatal Developmental Defects in Arabidopsis thaliana
title_sort lack of vacuolar h(+) -pyrophosphatase and cytosolic pyrophosphatases causes fatal developmental defects in arabidopsis thaliana
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266078/
https://www.ncbi.nlm.nih.gov/pubmed/32528505
http://dx.doi.org/10.3389/fpls.2020.00655
work_keys_str_mv AT fukudamayu lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT miedamarika lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT satoryosuke lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT kinoshitasatoru lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT tomoyamatakaaki lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT ferjaniali lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT maeshimamasayoshi lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana
AT segamishoji lackofvacuolarhpyrophosphataseandcytosolicpyrophosphatasescausesfataldevelopmentaldefectsinarabidopsisthaliana