Two iron-regulated transporter (IRT) genes showed differential expression in poplar trees under iron or zinc deficiency.
Identifieur interne : 001A76 ( Main/Exploration ); précédent : 001A75; suivant : 001A77Two iron-regulated transporter (IRT) genes showed differential expression in poplar trees under iron or zinc deficiency.
Auteurs : Danqiong Huang [États-Unis] ; Wenhao Dai [États-Unis]Source :
- Journal of plant physiology [ 1618-1328 ] ; 2015.
Descripteurs français
- KwdFr :
- Fer (déficit), Phylogenèse (MeSH), Populus (génétique), Populus (métabolisme), Protéines végétales (génétique), Protéines végétales (métabolisme), Régulation de l'expression des gènes végétaux (MeSH), Spécificité d'organe (MeSH), Test de complémentation (MeSH), Transporteurs de cations (génétique), Transporteurs de cations (métabolisme), Zinc (déficit).
- MESH :
- déficit : Fer, Zinc.
- génétique : Populus, Protéines végétales, Transporteurs de cations.
- métabolisme : Populus, Protéines végétales, Transporteurs de cations.
- Phylogenèse, Régulation de l'expression des gènes végétaux, Spécificité d'organe, Test de complémentation.
English descriptors
- KwdEn :
- Cation Transport Proteins (genetics), Cation Transport Proteins (metabolism), Gene Expression Regulation, Plant (MeSH), Genetic Complementation Test (MeSH), Iron (deficiency), Organ Specificity (MeSH), Phylogeny (MeSH), Plant Proteins (genetics), Plant Proteins (metabolism), Populus (genetics), Populus (metabolism), Zinc (deficiency).
- MESH :
- chemical , deficiency : Iron, Zinc.
- chemical , genetics : Cation Transport Proteins, Plant Proteins.
- chemical , metabolism : Cation Transport Proteins, Plant Proteins.
- genetics : Populus.
- metabolism : Populus.
- Gene Expression Regulation, Plant, Genetic Complementation Test, Organ Specificity, Phylogeny.
Abstract
Two iron-regulated transporter (IRT) genes were cloned from the iron chlorosis resistant (PtG) and susceptible (PtY) Populus tremula 'Erecta' lines. Nucleotide sequence analysis showed no significant difference between PtG and PtY. The predicted proteins contain a conserved ZIP domain with 8 transmembrane (TM) regions. A ZIP signature sequence was found in the fourth TM domain. Phylogenetic analysis revealed that PtIRT1 was clustered with tomato and tobacco IRT genes that are highly responsible to iron deficiency. The PtIRT3 gene was clustered with the AtIRT3 gene that was related to zinc and iron transport in plants. Tissue specific expression indicated that PtIRT1 only expressed in the root, while PtIRT3 constitutively expressed in all tested tissues. Under iron deficiency, the expression of PtIRT1 was dramatically increased and a significantly higher transcript level was detected in PtG than in PtY. Iron deficiency also enhanced the expression of PtIRT3 in PtG. On the other hand, zinc deficiency down-regulated the expression of PtIRT1 and PtIRT3 in both PtG and PtY. Zinc accumulated significantly under iron-deficient conditions, whereas the zinc deficiency showed no significant effect on iron accumulation. A yeast complementation test revealed that the PtIRT1 and PtIRT3 genes could restore the iron uptake ability under the iron uptake-deficiency condition. The results will help understand the mechanisms of iron deficiency response in poplar trees and other woody species.
DOI: 10.1016/j.jplph.2015.09.001
PubMed: 26373309
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Dai, Wenhao" sort="Dai, Wenhao" uniqKey="Dai W" first="Wenhao" last="Dai">Wenhao Dai</name>
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<series><title level="j">Journal of plant physiology</title>
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<term>Cation Transport Proteins (metabolism)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Genetic Complementation Test (MeSH)</term>
<term>Iron (deficiency)</term>
<term>Organ Specificity (MeSH)</term>
<term>Phylogeny (MeSH)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
<term>Zinc (deficiency)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Fer (déficit)</term>
<term>Phylogenèse (MeSH)</term>
<term>Populus (génétique)</term>
<term>Populus (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Spécificité d'organe (MeSH)</term>
<term>Test de complémentation (MeSH)</term>
<term>Transporteurs de cations (génétique)</term>
<term>Transporteurs de cations (métabolisme)</term>
<term>Zinc (déficit)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="deficiency" xml:lang="en"><term>Iron</term>
<term>Zinc</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Cation Transport Proteins</term>
<term>Plant Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Cation Transport Proteins</term>
<term>Plant Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="déficit" xml:lang="fr"><term>Fer</term>
<term>Zinc</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Populus</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Populus</term>
<term>Protéines végétales</term>
<term>Transporteurs de cations</term>
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<term>Transporteurs de cations</term>
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<term>Genetic Complementation Test</term>
<term>Organ Specificity</term>
<term>Phylogeny</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Phylogenèse</term>
<term>Régulation de l'expression des gènes végétaux</term>
<term>Spécificité d'organe</term>
<term>Test de complémentation</term>
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<front><div type="abstract" xml:lang="en">Two iron-regulated transporter (IRT) genes were cloned from the iron chlorosis resistant (PtG) and susceptible (PtY) Populus tremula 'Erecta' lines. Nucleotide sequence analysis showed no significant difference between PtG and PtY. The predicted proteins contain a conserved ZIP domain with 8 transmembrane (TM) regions. A ZIP signature sequence was found in the fourth TM domain. Phylogenetic analysis revealed that PtIRT1 was clustered with tomato and tobacco IRT genes that are highly responsible to iron deficiency. The PtIRT3 gene was clustered with the AtIRT3 gene that was related to zinc and iron transport in plants. Tissue specific expression indicated that PtIRT1 only expressed in the root, while PtIRT3 constitutively expressed in all tested tissues. Under iron deficiency, the expression of PtIRT1 was dramatically increased and a significantly higher transcript level was detected in PtG than in PtY. Iron deficiency also enhanced the expression of PtIRT3 in PtG. On the other hand, zinc deficiency down-regulated the expression of PtIRT1 and PtIRT3 in both PtG and PtY. Zinc accumulated significantly under iron-deficient conditions, whereas the zinc deficiency showed no significant effect on iron accumulation. A yeast complementation test revealed that the PtIRT1 and PtIRT3 genes could restore the iron uptake ability under the iron uptake-deficiency condition. The results will help understand the mechanisms of iron deficiency response in poplar trees and other woody species. </div>
</front>
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<Abstract><AbstractText>Two iron-regulated transporter (IRT) genes were cloned from the iron chlorosis resistant (PtG) and susceptible (PtY) Populus tremula 'Erecta' lines. Nucleotide sequence analysis showed no significant difference between PtG and PtY. The predicted proteins contain a conserved ZIP domain with 8 transmembrane (TM) regions. A ZIP signature sequence was found in the fourth TM domain. Phylogenetic analysis revealed that PtIRT1 was clustered with tomato and tobacco IRT genes that are highly responsible to iron deficiency. The PtIRT3 gene was clustered with the AtIRT3 gene that was related to zinc and iron transport in plants. Tissue specific expression indicated that PtIRT1 only expressed in the root, while PtIRT3 constitutively expressed in all tested tissues. Under iron deficiency, the expression of PtIRT1 was dramatically increased and a significantly higher transcript level was detected in PtG than in PtY. Iron deficiency also enhanced the expression of PtIRT3 in PtG. On the other hand, zinc deficiency down-regulated the expression of PtIRT1 and PtIRT3 in both PtG and PtY. Zinc accumulated significantly under iron-deficient conditions, whereas the zinc deficiency showed no significant effect on iron accumulation. A yeast complementation test revealed that the PtIRT1 and PtIRT3 genes could restore the iron uptake ability under the iron uptake-deficiency condition. The results will help understand the mechanisms of iron deficiency response in poplar trees and other woody species. </AbstractText>
<CopyrightInformation>Copyright © 2015 Elsevier GmbH. All rights reserved.</CopyrightInformation>
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