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Differential expression of a poplar copper chaperone gene in response to various abiotic stresses.

Identifieur interne : 004065 ( Main/Exploration ); précédent : 004064; suivant : 004066

Differential expression of a poplar copper chaperone gene in response to various abiotic stresses.

Auteurs : Hyoshin Lee [Corée du Sud] ; Jae-Soon Lee ; Eun-Kyung Bae ; Young-Im Choi ; Eun-Woon Noh

Source :

RBID : pubmed:15687088

Descripteurs français

English descriptors

Abstract

Copper chaperone (CCH) is upregulated during Arabidopsis (Arabidopsis thaliana L. Columbia) leaf senescence, suggesting that it mobilizes certain metal ions in leaves and transports them to other growing parts of the plants. The CCHs are also involved in defense mechanisms against oxidative stress in Arabidopsis and tomato (Lycopersicon esculentum Mill. cv. 'Ailsa Craig'). To elucidate the functions of CCH in poplar, we cloned a CCH gene (PoCCH) from Populus (Populus alba x P. tremula var. glandulosa) suspension cells and tested its expression in response to various treatments including heavy metals, plant growth regulators and abiotic stresses. The PoCCH cDNA is 540 bp in length, including a 55-bp 5' noncoding domain, a 258-bp open reading frame (ORF), and 227-bp 3' termination region. The coding region of PoCCH represents a putative 85-amino-acid protein with a molecular weight of 8.9 kDa. The deduced amino acid sequence of the PoCCH gene product is 87 and 78% identical to those of tomato and Arabidopsis, respectively, with a high degree of conservation in both the metal-binding and lysine-rich regions. However, the PoCCH gene product lacks the C-terminal extension identified in Arabidopsis CCH. Southern blot analysis suggested that the PoCCH gene is present in low copy numbers in poplar. The expression of PoCCH increased under copper deprivation conditions. The expression of PoCCH was down-regulated by high concentrations of copper, whereas some metals, such as aluminum and zinc, markedly induced PoCCH, and others including cadmium, cobalt and lead had little effect on PoCCH expression. The plant growth regulator jasmonic acid caused an increase in PoCCH transcript whereas abscisic acid, salicylic acid and gibberellic acid did not. The gene was highly induced when cells were exposed to physical stress by high-speed agitation on a gyratory shaker. Other effective inducers of PoCCH expression in suspension culture were methyl viologen and NaCl. Thus, PoCCH does not respond to all stresses, but responds specifically to certain metals and abiotic stresses that induce oxidative damage. Our results suggest that JA is involved in regulating PoCCH expression in poplar cells.

DOI: 10.1093/treephys/25.4.395
PubMed: 15687088


Affiliations:


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Le document en format XML

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<term>Adaptation, Physiological (genetics)</term>
<term>Amino Acid Sequence (MeSH)</term>
<term>Arabidopsis Proteins (genetics)</term>
<term>Base Sequence (MeSH)</term>
<term>Copper (metabolism)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Genome, Plant (MeSH)</term>
<term>Metals, Heavy (metabolism)</term>
<term>Molecular Chaperones (genetics)</term>
<term>Molecular Chaperones (metabolism)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Plant Growth Regulators (metabolism)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
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<term>Stress, Mechanical (MeSH)</term>
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<term>Adaptation physiologique (génétique)</term>
<term>Analyse de séquence d'ADN (MeSH)</term>
<term>Chaperons moléculaires (génétique)</term>
<term>Chaperons moléculaires (métabolisme)</term>
<term>Contrainte mécanique (MeSH)</term>
<term>Cuivre (métabolisme)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Facteur de croissance végétal (métabolisme)</term>
<term>Génome végétal (MeSH)</term>
<term>Métaux lourds (métabolisme)</term>
<term>Populus (génétique)</term>
<term>Populus (métabolisme)</term>
<term>Protéines d'Arabidopsis (génétique)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Séquence nucléotidique (MeSH)</term>
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<term>Chaperons moléculaires</term>
<term>Populus</term>
<term>Protéines d'Arabidopsis</term>
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<term>Copper</term>
<term>Metals, Heavy</term>
<term>Molecular Chaperones</term>
<term>Plant Growth Regulators</term>
<term>Populus</term>
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<term>Chaperons moléculaires</term>
<term>Cuivre</term>
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<term>Métaux lourds</term>
<term>Populus</term>
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<term>Amino Acid Sequence</term>
<term>Base Sequence</term>
<term>Gene Expression Regulation, Plant</term>
<term>Genome, Plant</term>
<term>Molecular Sequence Data</term>
<term>Sequence Analysis, DNA</term>
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<div type="abstract" xml:lang="en">Copper chaperone (CCH) is upregulated during Arabidopsis (Arabidopsis thaliana L. Columbia) leaf senescence, suggesting that it mobilizes certain metal ions in leaves and transports them to other growing parts of the plants. The CCHs are also involved in defense mechanisms against oxidative stress in Arabidopsis and tomato (Lycopersicon esculentum Mill. cv. 'Ailsa Craig'). To elucidate the functions of CCH in poplar, we cloned a CCH gene (PoCCH) from Populus (Populus alba x P. tremula var. glandulosa) suspension cells and tested its expression in response to various treatments including heavy metals, plant growth regulators and abiotic stresses. The PoCCH cDNA is 540 bp in length, including a 55-bp 5' noncoding domain, a 258-bp open reading frame (ORF), and 227-bp 3' termination region. The coding region of PoCCH represents a putative 85-amino-acid protein with a molecular weight of 8.9 kDa. The deduced amino acid sequence of the PoCCH gene product is 87 and 78% identical to those of tomato and Arabidopsis, respectively, with a high degree of conservation in both the metal-binding and lysine-rich regions. However, the PoCCH gene product lacks the C-terminal extension identified in Arabidopsis CCH. Southern blot analysis suggested that the PoCCH gene is present in low copy numbers in poplar. The expression of PoCCH increased under copper deprivation conditions. The expression of PoCCH was down-regulated by high concentrations of copper, whereas some metals, such as aluminum and zinc, markedly induced PoCCH, and others including cadmium, cobalt and lead had little effect on PoCCH expression. The plant growth regulator jasmonic acid caused an increase in PoCCH transcript whereas abscisic acid, salicylic acid and gibberellic acid did not. The gene was highly induced when cells were exposed to physical stress by high-speed agitation on a gyratory shaker. Other effective inducers of PoCCH expression in suspension culture were methyl viologen and NaCl. Thus, PoCCH does not respond to all stresses, but responds specifically to certain metals and abiotic stresses that induce oxidative damage. Our results suggest that JA is involved in regulating PoCCH expression in poplar cells.</div>
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