PoplarV1, Main, Exploration, bibRecord, 003F74

Polar-localised poplar K+ channel capable of controlling electrical properties of wood-forming cells.

Identifieur interne : 003F74 ( Main/Exploration ); précédent : 003F73; suivant : 003F75

Polar-localised poplar K+ channel capable of controlling electrical properties of wood-forming cells.

Auteurs : Matthias Arend [Allemagne] ; Andrea Stinzing ; Christa Wind ; Katharina Langer ; Andreas Latz ; Peter Ache ; Jörg Fromm ; Rainer Hedrich

Source :

Planta [ 0032-0935 ] ; 2005.

RBID : pubmed:16258747

Descripteurs français

KwdFr :
- Anticorps (immunologie), Arabidopsis (génétique), Bois (MeSH), Canaux potassiques de la superfamille Shaker (analyse), Canaux potassiques de la superfamille Shaker (génétique), Données de séquences moléculaires (MeSH), Expression des gènes (MeSH), Populus (cytologie), Populus (génétique), Populus (immunologie), Populus (métabolisme), Protoplastes (MeSH), Régions promotrices (génétique) (MeSH), Séquence d'acides aminés (MeSH), Technique d'immunofluorescence (MeSH), Techniques de patch-clamp (MeSH), Tiges de plante (cytologie), Tiges de plante (physiologie), Végétaux génétiquement modifiés (MeSH), Électrophysiologie (MeSH).
MESH :
- analyse : Canaux potassiques de la superfamille Shaker.
- cytologie : Populus, Tiges de plante.
- génétique : Arabidopsis, Canaux potassiques de la superfamille Shaker, Populus.
- immunologie : Anticorps, Populus.
- métabolisme : Populus.
- physiologie : Tiges de plante.
- Bois, Données de séquences moléculaires, Expression des gènes, Protoplastes, Régions promotrices (génétique), Séquence d'acides aminés, Technique d'immunofluorescence, Techniques de patch-clamp, Végétaux génétiquement modifiés, Électrophysiologie.

English descriptors

KwdEn :
- Amino Acid Sequence (MeSH), Antibodies (immunology), Arabidopsis (genetics), Electrophysiology (MeSH), Fluorescent Antibody Technique (MeSH), Gene Expression (MeSH), Molecular Sequence Data (MeSH), Patch-Clamp Techniques (MeSH), Plant Stems (cytology), Plant Stems (physiology), Plants, Genetically Modified (MeSH), Populus (cytology), Populus (genetics), Populus (immunology), Populus (metabolism), Promoter Regions, Genetic (MeSH), Protoplasts (MeSH), Shaker Superfamily of Potassium Channels (analysis), Shaker Superfamily of Potassium Channels (genetics), Wood (MeSH).
MESH :
- chemical , analysis : Shaker Superfamily of Potassium Channels.
- chemical , genetics : Shaker Superfamily of Potassium Channels.
- chemical , immunology : Antibodies.
- cytology : Plant Stems, Populus.
- genetics : Arabidopsis, Populus.
- immunology : Populus.
- metabolism : Populus.
- physiology : Plant Stems.
- Amino Acid Sequence, Electrophysiology, Fluorescent Antibody Technique, Gene Expression, Molecular Sequence Data, Patch-Clamp Techniques, Plants, Genetically Modified, Promoter Regions, Genetic, Protoplasts, Wood.

Abstract

In previous studies, we have shown that annual expression profiles of cambial and wood tissue with respect to the Shaker K+ channel PTORK correlate with cambial activity. To follow PTORK-gene activity on the cellular level, we isolated the respective promoter regions and generated transgenic Arabidopsis plants expressing the GUS gene under the control of the PTORK promoter. Cross-sections of petioles showed PTORK-driven signals predominantly in the xylem parenchyma surrounding the vessels and in the phloem. Antibodies raised against a unique N-terminal region of PTORK in histo-immunochemical analyses recognised this K+-release channel in growth-active poplar plants only. PTORK labelling was found in differentiating xylem cells (young fibres) and mature xylem (vessel-associated cells of the ray parenchyma). Patch-clamp measurements on fibre cell protoplasts, derived from young poplar twigs, identified outward-rectifying K+ channels as the major K+ conductance of this cell type, which resembled the biophysical properties of PTORK when expressed in Xenopus oocytes.

DOI: 10.1007/s00425-005-0122-y
PubMed: 16258747

Affiliations:

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 003F32
to stream Main, to step Curation: 003F32

Le document en format XML

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<term>Données de séquences moléculaires</term>
<term>Expression des gènes</term>
<term>Protoplastes</term>
<term>Régions promotrices (génétique)</term>
<term>Séquence d'acides aminés</term>
<term>Technique d'immunofluorescence</term>
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<front><div type="abstract" xml:lang="en">In previous studies, we have shown that annual expression profiles of cambial and wood tissue with respect to the Shaker K+ channel PTORK correlate with cambial activity. To follow PTORK-gene activity on the cellular level, we isolated the respective promoter regions and generated transgenic Arabidopsis plants expressing the GUS gene under the control of the PTORK promoter. Cross-sections of petioles showed PTORK-driven signals predominantly in the xylem parenchyma surrounding the vessels and in the phloem. Antibodies raised against a unique N-terminal region of PTORK in histo-immunochemical analyses recognised this K+-release channel in growth-active poplar plants only. PTORK labelling was found in differentiating xylem cells (young fibres) and mature xylem (vessel-associated cells of the ray parenchyma). Patch-clamp measurements on fibre cell protoplasts, derived from young poplar twigs, identified outward-rectifying K+ channels as the major K+ conductance of this cell type, which resembled the biophysical properties of PTORK when expressed in Xenopus oocytes.</div>
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<Abstract><AbstractText>In previous studies, we have shown that annual expression profiles of cambial and wood tissue with respect to the Shaker K+ channel PTORK correlate with cambial activity. To follow PTORK-gene activity on the cellular level, we isolated the respective promoter regions and generated transgenic Arabidopsis plants expressing the GUS gene under the control of the PTORK promoter. Cross-sections of petioles showed PTORK-driven signals predominantly in the xylem parenchyma surrounding the vessels and in the phloem. Antibodies raised against a unique N-terminal region of PTORK in histo-immunochemical analyses recognised this K+-release channel in growth-active poplar plants only. PTORK labelling was found in differentiating xylem cells (young fibres) and mature xylem (vessel-associated cells of the ray parenchyma). Patch-clamp measurements on fibre cell protoplasts, derived from young poplar twigs, identified outward-rectifying K+ channels as the major K+ conductance of this cell type, which resembled the biophysical properties of PTORK when expressed in Xenopus oocytes.</AbstractText>
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<li>District de Haute-Bavière</li>
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<tree><noCountry><name sortKey="Ache, Peter" sort="Ache, Peter" uniqKey="Ache P" first="Peter" last="Ache">Peter Ache</name>
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   |texte=   Polar-localised poplar K+ channel capable of controlling electrical properties of wood-forming cells.
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Polar-localised poplar K+ channel capable of controlling electrical properties of wood-forming cells.

Polar-localised poplar K+ channel capable of controlling electrical properties of wood-forming cells.

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