Physiological and molecular mechanisms mediating xylem Na+ loading in barley in the context of salinity stress tolerance

Time‐dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive varieties were less efficient in controlling xylem Na+ loading and showed a gradual increase in the xylem Na+ content over the time. To under...

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Published inPlant, cell and environment Vol. 40; no. 7; pp. 1009 - 1020
Main Authors Zhu, Min, Zhou, Meixue, Shabala, Lana, Shabala, Sergey
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.07.2017
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Abstract Time‐dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive varieties were less efficient in controlling xylem Na+ loading and showed a gradual increase in the xylem Na+ content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca2+, K+ and Na+ were measured from the xylem parenchyma tissue in response to H2O2 and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase‐mediated apoplastic H2O2 production acts upstream of the xylem Na+ loading and is causally related to ROS‐inducible Ca2+ uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na+ retrieval from the xylem and the significant reduction of Na+ and K+ fluxes induced by bumetanide are indicative of a major role of chloride cation co‐transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na+/K+ movement into/out of xylem.
AbstractList Time-dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt-sensitive varieties were less efficient in controlling xylem Na+ loading and showed a gradual increase in the xylem Na+ content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca2+ , K+ and Na+ were measured from the xylem parenchyma tissue in response to H2 O2 and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase-mediated apoplastic H2 O2 production acts upstream of the xylem Na+ loading and is causally related to ROS-inducible Ca2+ uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na+ retrieval from the xylem and the significant reduction of Na+ and K+ fluxes induced by bumetanide are indicative of a major role of chloride cation co-transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na+ /K+ movement into/out of xylem.Time-dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt-sensitive varieties were less efficient in controlling xylem Na+ loading and showed a gradual increase in the xylem Na+ content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca2+ , K+ and Na+ were measured from the xylem parenchyma tissue in response to H2 O2 and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase-mediated apoplastic H2 O2 production acts upstream of the xylem Na+ loading and is causally related to ROS-inducible Ca2+ uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na+ retrieval from the xylem and the significant reduction of Na+ and K+ fluxes induced by bumetanide are indicative of a major role of chloride cation co-transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na+ /K+ movement into/out of xylem.
Time‐dependent kinetics of xylem Na⁺ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive varieties were less efficient in controlling xylem Na⁺ loading and showed a gradual increase in the xylem Na⁺ content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca²⁺, K⁺ and Na⁺ were measured from the xylem parenchyma tissue in response to H₂O₂ and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase‐mediated apoplastic H₂O₂ production acts upstream of the xylem Na⁺ loading and is causally related to ROS‐inducible Ca²⁺ uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na⁺ retrieval from the xylem and the significant reduction of Na⁺ and K⁺ fluxes induced by bumetanide are indicative of a major role of chloride cation co‐transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na⁺/K⁺ movement into/out of xylem.
Time-dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt-sensitive varieties were less efficient in controlling xylem Na+ loading and showed a gradual increase in the xylem Na+ content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca2+, K+ and Na+ were measured from the xylem parenchyma tissue in response to H2O2 and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase-mediated apoplastic H2O2 production acts upstream of the xylem Na+ loading and is causally related to ROS-inducible Ca2+ uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na+ retrieval from the xylem and the significant reduction of Na+ and K+ fluxes induced by bumetanide are indicative of a major role of chloride cation co-transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na+/K+ movement into/out of xylem.
Time‐dependent kinetics of xylem Na + loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive varieties were less efficient in controlling xylem Na + loading and showed a gradual increase in the xylem Na + content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca 2+ , K + and Na + were measured from the xylem parenchyma tissue in response to H 2 O 2 and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase‐mediated apoplastic H 2 O 2 production acts upstream of the xylem Na + loading and is causally related to ROS‐inducible Ca 2+ uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na + retrieval from the xylem and the significant reduction of Na + and K + fluxes induced by bumetanide are indicative of a major role of chloride cation co‐transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na + /K + movement into/out of xylem.
Time-dependent kinetics of xylem Na loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt-sensitive varieties were less efficient in controlling xylem Na loading and showed a gradual increase in the xylem Na content over the time. To understand underlying ionic and molecular mechanisms, net fluxes of Ca , K and Na were measured from the xylem parenchyma tissue in response to H O and ABA; both of them associated with salinity stress signalling. Our results indicate that NADPH oxidase-mediated apoplastic H O production acts upstream of the xylem Na loading and is causally related to ROS-inducible Ca uptake systems in the root stelar tissue. It was also found that ABA regulates (directly or indirectly) the process of Na retrieval from the xylem and the significant reduction of Na and K fluxes induced by bumetanide are indicative of a major role of chloride cation co-transporter (CCC) on xylem ion loading. Transcript levels of HvHKT1;5_like and HvSOS1_like genes in the root stele were observed to decrease after salt stress, while there was an increase in HvSKOR_like gene, indicating that these ion transporters are involved in primary Na /K movement into/out of xylem.
Author Shabala, Sergey
Zhu, Min
Zhou, Meixue
Shabala, Lana
Author_xml – sequence: 1
  givenname: Min
  surname: Zhu
  fullname: Zhu, Min
  organization: University of Tasmania
– sequence: 2
  givenname: Meixue
  surname: Zhou
  fullname: Zhou, Meixue
  organization: University of Tasmania
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  givenname: Lana
  surname: Shabala
  fullname: Shabala, Lana
  organization: University of Tasmania
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  givenname: Sergey
  surname: Shabala
  fullname: Shabala, Sergey
  email: sergey.shabala@utas.edu.au
  organization: University of Tasmania
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26881809$$D View this record in MEDLINE/PubMed
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Keywords ABA
CCC transporter
NADPH oxidase
xylem sodium loading
H2O2
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2009; 36
2014; 80
2015; 27
1992; 258
2002; 128
2006; 142
2008; 377
2013; 170
1985; 78
2014; 33
2005; 56
2003; 21
2003; 22
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e_1_2_6_10_1
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Munns R. (e_1_2_6_40_1) 2015; 10
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e_1_2_6_21_1
e_1_2_6_61_1
Wind S. (e_1_2_6_66_1) 2008; 377
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e_1_2_6_46_1
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SSID ssj0001479
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Snippet Time‐dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive...
Time‐dependent kinetics of xylem Na + loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive...
Time-dependent kinetics of xylem Na loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt-sensitive...
Time-dependent kinetics of xylem Na+ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt-sensitive...
Time‐dependent kinetics of xylem Na⁺ loading was investigated using a large number of barley genotypes contrasting in their salinity tolerance. Salt‐sensitive...
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SubjectTerms ABA
Abscisic acid
Abscisic Acid - metabolism
Abscisic Acid - pharmacology
Barley
Bumetanide
Calcium
Calcium influx
cations
CCC transporter
Chlorides
Fluxes
Gene Expression Regulation, Plant
genes
genotype
Genotypes
H2O2
Hordeum - drug effects
Hordeum - genetics
Hordeum - physiology
Hydrogen peroxide
Hydrogen Peroxide - pharmacology
Molecular modelling
NAD(P)H oxidase
NADP (coenzyme)
NADPH oxidase
Oxidase
Parenchyma
parenchyma (plant tissue)
Plant Proteins - genetics
Plant Proteins - metabolism
potassium
Potassium - metabolism
Reactive oxygen species
Salinity
Salinity effects
Salinity tolerance
salt stress
salt tolerance
Signaling
SKOR
sodium
Sodium - metabolism
SOS1
stele
stress tolerance
Stress, Physiological - physiology
Stresses
Thiourea - pharmacology
Transcription
transporters
Xylem
Xylem - drug effects
Xylem - metabolism
xylem sodium loading
Title Physiological and molecular mechanisms mediating xylem Na+ loading in barley in the context of salinity stress tolerance
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fpce.12727
https://www.ncbi.nlm.nih.gov/pubmed/26881809
https://www.proquest.com/docview/1929859853
https://www.proquest.com/docview/1826652120
https://www.proquest.com/docview/2000499275
Volume 40
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