Molecular changes associated with the setting up of secondary growth in aspen.
Identifieur interne : 003F97 ( Main/Exploration ); précédent : 003F96; suivant : 003F98Molecular changes associated with the setting up of secondary growth in aspen.
Auteurs : Damien Van Raemdonck [Belgique] ; Edouard Pesquet ; Sophie Cloquet ; Hans Beeckman ; Wout Boerjan ; Deborah Goffner ; Mondher El Jaziri ; Marie BaucherSource :
- Journal of experimental botany [ 0022-0957 ] ; 2005.
Descripteurs français
- KwdFr :
- ADN complémentaire (métabolisme), ADN des plantes (métabolisme), Alignement de séquences (MeSH), Analyse de profil d'expression de gènes (MeSH), Données de séquences moléculaires (MeSH), Populus (croissance et développement), Populus (métabolisme), Protéines végétales (MeSH), Régulation de l'expression des gènes au cours du développement (physiologie), Régulation de l'expression des gènes végétaux (physiologie), Similitude de séquences d'acides aminés (MeSH), Séquence d'acides aminés (MeSH), Tiges de plante (croissance et développement), Tiges de plante (métabolisme).
- MESH :
- croissance et développement : Populus, Tiges de plante.
- métabolisme : ADN complémentaire, ADN des plantes, Populus, Tiges de plante.
- physiologie : Régulation de l'expression des gènes au cours du développement, Régulation de l'expression des gènes végétaux.
- Alignement de séquences, Analyse de profil d'expression de gènes, Données de séquences moléculaires, Protéines végétales, Similitude de séquences d'acides aminés, Séquence d'acides aminés.
English descriptors
- KwdEn :
- Amino Acid Sequence (MeSH), DNA, Complementary (metabolism), DNA, Plant (metabolism), Gene Expression Profiling (MeSH), Gene Expression Regulation, Developmental (physiology), Gene Expression Regulation, Plant (physiology), Molecular Sequence Data (MeSH), Plant Proteins (MeSH), Plant Stems (growth & development), Plant Stems (metabolism), Populus (growth & development), Populus (metabolism), Sequence Alignment (MeSH), Sequence Homology, Amino Acid (MeSH).
- MESH :
- chemical , metabolism : DNA, Complementary, DNA, Plant.
- growth & development : Plant Stems, Populus.
- metabolism : Plant Stems, Populus.
- physiology : Gene Expression Regulation, Developmental, Gene Expression Regulation, Plant.
- Amino Acid Sequence, Gene Expression Profiling, Molecular Sequence Data, Plant Proteins, Sequence Alignment, Sequence Homology, Amino Acid.
Abstract
Vascular secondary growth results from the activity of the vascular cambium, which produces secondary phloem and secondary xylem. By means of cDNA-amplified fragment length polymorphism (cDNA-AFLP) analysis along aspen stems, several potential regulatory genes involved in the progressive transition from primary to secondary growth were identified. A total of 83 unique transcript-derived fragments (TDFs) was found to be differentiated between the top and the bottom of the stem. An independent RT-PCR expression analysis validated the cDNA-AFLP profiles for 19 of the TDFs. Among these, seven correspond to new genes encoding putative regulatory proteins. Emphasis was laid upon two genes encoding, respectively, an AP2/ERF-like transcription factor (PtaERF1) and a RING finger protein (PtaRHE1); their differential expression was further confirmed by reverse northern analysis. In situ RT-PCR revealed that PtaERF1 was expressed in phloem tissue and that PtaRHE1 had a pronounced expression in ray initials and their derivatives within the cambial zone. These results suggest that these genes have a potential role in vascular tissue development and/or functioning.
DOI: 10.1093/jxb/eri221
PubMed: 15996985
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<term>Gene Expression Regulation, Developmental (physiology)</term>
<term>Gene Expression Regulation, Plant (physiology)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Plant Proteins (MeSH)</term>
<term>Plant Stems (growth & development)</term>
<term>Plant Stems (metabolism)</term>
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<term>Populus (metabolism)</term>
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<term>Populus (métabolisme)</term>
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<term>Régulation de l'expression des gènes végétaux (physiologie)</term>
<term>Similitude de séquences d'acides aminés (MeSH)</term>
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<term>Tiges de plante (métabolisme)</term>
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<front><div type="abstract" xml:lang="en">Vascular secondary growth results from the activity of the vascular cambium, which produces secondary phloem and secondary xylem. By means of cDNA-amplified fragment length polymorphism (cDNA-AFLP) analysis along aspen stems, several potential regulatory genes involved in the progressive transition from primary to secondary growth were identified. A total of 83 unique transcript-derived fragments (TDFs) was found to be differentiated between the top and the bottom of the stem. An independent RT-PCR expression analysis validated the cDNA-AFLP profiles for 19 of the TDFs. Among these, seven correspond to new genes encoding putative regulatory proteins. Emphasis was laid upon two genes encoding, respectively, an AP2/ERF-like transcription factor (PtaERF1) and a RING finger protein (PtaRHE1); their differential expression was further confirmed by reverse northern analysis. In situ RT-PCR revealed that PtaERF1 was expressed in phloem tissue and that PtaRHE1 had a pronounced expression in ray initials and their derivatives within the cambial zone. These results suggest that these genes have a potential role in vascular tissue development and/or functioning.</div>
</front>
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<Abstract><AbstractText>Vascular secondary growth results from the activity of the vascular cambium, which produces secondary phloem and secondary xylem. By means of cDNA-amplified fragment length polymorphism (cDNA-AFLP) analysis along aspen stems, several potential regulatory genes involved in the progressive transition from primary to secondary growth were identified. A total of 83 unique transcript-derived fragments (TDFs) was found to be differentiated between the top and the bottom of the stem. An independent RT-PCR expression analysis validated the cDNA-AFLP profiles for 19 of the TDFs. Among these, seven correspond to new genes encoding putative regulatory proteins. Emphasis was laid upon two genes encoding, respectively, an AP2/ERF-like transcription factor (PtaERF1) and a RING finger protein (PtaRHE1); their differential expression was further confirmed by reverse northern analysis. In situ RT-PCR revealed that PtaERF1 was expressed in phloem tissue and that PtaRHE1 had a pronounced expression in ray initials and their derivatives within the cambial zone. These results suggest that these genes have a potential role in vascular tissue development and/or functioning.</AbstractText>
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