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Overexpression of two PsnAP1 genes from Populus simonii × P. nigra causes early flowering in transgenic tobacco and Arabidopsis.

Identifieur interne : 002115 ( Main/Exploration ); précédent : 002114; suivant : 002116

Overexpression of two PsnAP1 genes from Populus simonii × P. nigra causes early flowering in transgenic tobacco and Arabidopsis.

Auteurs : Tangchun Zheng [République populaire de Chine] ; Shuang Li [République populaire de Chine] ; Lina Zang [République populaire de Chine] ; Lijuan Dai [République populaire de Chine] ; Chuanping Yang [République populaire de Chine] ; Guan-Zheng Qu [République populaire de Chine]

Source :

RBID : pubmed:25360739

Descripteurs français

English descriptors

Abstract

In Arabidopsis, AP1 is a floral meristem identity gene and plays an important role in floral organ development. In this study, PsnAP1-1 and PsnAP1-2 were isolated from the male reproductive buds of poplar (Populus simonii × P. nigra), which are the orthologs of AP1 in Arabidopsis, by sequence analysis. Northern blot and qRT-PCR analysis showed that PsnAP1-1 and PsnAP1-2 exhibited high expression level in early inflorescence development of poplar. Subcellular localization showed the PsnAP1-1 and PsnAP1-2 proteins are localized in the nucleus. Overexpression of PsnAP1-1 and PsnAP1-2 in tobacco under the control of a CaMV 35S promoter significantly enhanced early flowering. These transgenic plants also showed much earlier stem initiation and higher rates of photosynthesis than did wild-type tobacco. qRT-PCR analysis further indicated that overexpression of PsnAP1-1 and PsnAP1-2 resulted in up-regulation of genes related to flowering, such as NtMADS4, NtMADS5 and NtMADS11. Overexpression of PsnAP1-1 and PsnAP1-2 in Arabidopsis also induced early flowering, but did not complement the ap1-10 floral morphology to any noticeable extent. This study indicates that PsnAP1-1 and PsnAP1-2 play a role in floral transition of poplar.

DOI: 10.1371/journal.pone.0111725
PubMed: 25360739
PubMed Central: PMC4216142


Affiliations:


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Le document en format XML

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<term>Blotting, Northern (MeSH)</term>
<term>Chlorophyll (metabolism)</term>
<term>Crosses, Genetic (MeSH)</term>
<term>Flowers (genetics)</term>
<term>Flowers (physiology)</term>
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<term>Genes, Plant (MeSH)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Mutation (genetics)</term>
<term>Phenotype (MeSH)</term>
<term>Photosynthesis (MeSH)</term>
<term>Plant Proteins (chemistry)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (isolation & purification)</term>
<term>Plants, Genetically Modified (MeSH)</term>
<term>Populus (genetics)</term>
<term>Protein Transport (MeSH)</term>
<term>Sequence Alignment (MeSH)</term>
<term>Subcellular Fractions (metabolism)</term>
<term>Tobacco (genetics)</term>
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<term>Analyse de profil d'expression de gènes (MeSH)</term>
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<term>Chlorophylle (métabolisme)</term>
<term>Croisements génétiques (MeSH)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Fleurs (génétique)</term>
<term>Fleurs (physiologie)</term>
<term>Fractions subcellulaires (métabolisme)</term>
<term>Gènes de plante (MeSH)</term>
<term>Mutation (génétique)</term>
<term>Photosynthèse (MeSH)</term>
<term>Phénotype (MeSH)</term>
<term>Populus (génétique)</term>
<term>Protéines végétales (composition chimique)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (isolement et purification)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Tabac (génétique)</term>
<term>Technique de Northern (MeSH)</term>
<term>Transport des protéines (MeSH)</term>
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<term>Protéines végétales</term>
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<term>Arabidopsis</term>
<term>Flowers</term>
<term>Mutation</term>
<term>Populus</term>
<term>Tobacco</term>
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<term>Protéines végétales</term>
<term>Tabac</term>
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<term>Protéines végétales</term>
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<term>Subcellular Fractions</term>
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<term>Chlorophylle</term>
<term>Fractions subcellulaires</term>
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<term>Fleurs</term>
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<term>Flowers</term>
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<term>Molecular Sequence Data</term>
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<term>Protein Transport</term>
<term>Sequence Alignment</term>
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<term>Analyse de profil d'expression de gènes</term>
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<term>Séquence d'acides aminés</term>
<term>Technique de Northern</term>
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<div type="abstract" xml:lang="en">In Arabidopsis, AP1 is a floral meristem identity gene and plays an important role in floral organ development. In this study, PsnAP1-1 and PsnAP1-2 were isolated from the male reproductive buds of poplar (Populus simonii × P. nigra), which are the orthologs of AP1 in Arabidopsis, by sequence analysis. Northern blot and qRT-PCR analysis showed that PsnAP1-1 and PsnAP1-2 exhibited high expression level in early inflorescence development of poplar. Subcellular localization showed the PsnAP1-1 and PsnAP1-2 proteins are localized in the nucleus. Overexpression of PsnAP1-1 and PsnAP1-2 in tobacco under the control of a CaMV 35S promoter significantly enhanced early flowering. These transgenic plants also showed much earlier stem initiation and higher rates of photosynthesis than did wild-type tobacco. qRT-PCR analysis further indicated that overexpression of PsnAP1-1 and PsnAP1-2 resulted in up-regulation of genes related to flowering, such as NtMADS4, NtMADS5 and NtMADS11. Overexpression of PsnAP1-1 and PsnAP1-2 in Arabidopsis also induced early flowering, but did not complement the ap1-10 floral morphology to any noticeable extent. This study indicates that PsnAP1-1 and PsnAP1-2 play a role in floral transition of poplar. </div>
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<AbstractText>In Arabidopsis, AP1 is a floral meristem identity gene and plays an important role in floral organ development. In this study, PsnAP1-1 and PsnAP1-2 were isolated from the male reproductive buds of poplar (Populus simonii × P. nigra), which are the orthologs of AP1 in Arabidopsis, by sequence analysis. Northern blot and qRT-PCR analysis showed that PsnAP1-1 and PsnAP1-2 exhibited high expression level in early inflorescence development of poplar. Subcellular localization showed the PsnAP1-1 and PsnAP1-2 proteins are localized in the nucleus. Overexpression of PsnAP1-1 and PsnAP1-2 in tobacco under the control of a CaMV 35S promoter significantly enhanced early flowering. These transgenic plants also showed much earlier stem initiation and higher rates of photosynthesis than did wild-type tobacco. qRT-PCR analysis further indicated that overexpression of PsnAP1-1 and PsnAP1-2 resulted in up-regulation of genes related to flowering, such as NtMADS4, NtMADS5 and NtMADS11. Overexpression of PsnAP1-1 and PsnAP1-2 in Arabidopsis also induced early flowering, but did not complement the ap1-10 floral morphology to any noticeable extent. This study indicates that PsnAP1-1 and PsnAP1-2 play a role in floral transition of poplar. </AbstractText>
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