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Agrobacterium-mediated transient MaFT expression in mulberry (Morus alba L.) leaves.

Identifieur interne : 000337 ( Main/Corpus ); précédent : 000336; suivant : 000338

Agrobacterium-mediated transient MaFT expression in mulberry (Morus alba L.) leaves.

Auteurs : Su-Li Wu ; Xiao-Bing Yang ; Li-Qun Liu ; Tao Jiang ; Hai Wu ; Chao Su ; Yong-Hua Qian ; Feng Jiao

Source :

RBID : pubmed:26024368

English descriptors

Abstract

To optimize Agrobacterium-mediated transient transformation assay in mulberry (Morus alba L.), various infiltration methods, Agrobacterium tumefaciens (A. tumefaciens) strains, and bacterial concentrations were tested in mulberry seedlings. Compared with LBA4404, GV3101 harboring pBE2133 plasmids presented stronger GUS signals at 3 days post infiltration using syringe. Recombinant plasmids pBE2133:GFP and pBE2133:GFP:MaFT were successfully constructed. Transient expression of MaFT:GFP protein was found in leaves, petiole (cross section), and shoot apical meristem (SAM) of mulberry according to the GFP signal. Moreover, MaFT:GFP mRNA was also detected in leaves and SAM via RT-PCR and qRT-PCR. An efficient transient transformation system could be achieved in mulberry seedlings by syringe using A. tumefaciens GV3101 at the OD600 of 0.5. The movement of MaFT expression from leaves to SAM might trigger the precocious flowering of mulberry.

DOI: 10.1080/09168451.2015.1025691
PubMed: 26024368

Links to Exploration step

pubmed:26024368

Le document en format XML

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<name sortKey="Wu, Su Li" sort="Wu, Su Li" uniqKey="Wu S" first="Su-Li" last="Wu">Su-Li Wu</name>
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<nlm:affiliation>Institute of Sericulture and Silk , Northwest A&F University, Yangling, P.R. China. fjao@nwsuaf.edu.cn</nlm:affiliation>
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<name sortKey="Yang, Xiao Bing" sort="Yang, Xiao Bing" uniqKey="Yang X" first="Xiao-Bing" last="Yang">Xiao-Bing Yang</name>
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<name sortKey="Liu, Li Qun" sort="Liu, Li Qun" uniqKey="Liu L" first="Li-Qun" last="Liu">Li-Qun Liu</name>
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<name sortKey="Jiang, Tao" sort="Jiang, Tao" uniqKey="Jiang T" first="Tao" last="Jiang">Tao Jiang</name>
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<name sortKey="Wu, Hai" sort="Wu, Hai" uniqKey="Wu H" first="Hai" last="Wu">Hai Wu</name>
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<name sortKey="Su, Chao" sort="Su, Chao" uniqKey="Su C" first="Chao" last="Su">Chao Su</name>
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<term>Arabidopsis Proteins (genetics)</term>
<term>Fruit (genetics)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Morus (genetics)</term>
<term>Morus (growth & development)</term>
<term>Plant Leaves (genetics)</term>
<term>Plant Leaves (growth & development)</term>
<term>Plants, Genetically Modified (genetics)</term>
<term>Plants, Genetically Modified (growth & development)</term>
<term>Plasmids (MeSH)</term>
<term>Seedlings (genetics)</term>
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<term>Arabidopsis Proteins</term>
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<term>Agrobacterium tumefaciens</term>
<term>Arabidopsis</term>
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<div type="abstract" xml:lang="en">To optimize Agrobacterium-mediated transient transformation assay in mulberry (Morus alba L.), various infiltration methods, Agrobacterium tumefaciens (A. tumefaciens) strains, and bacterial concentrations were tested in mulberry seedlings. Compared with LBA4404, GV3101 harboring pBE2133 plasmids presented stronger GUS signals at 3 days post infiltration using syringe. Recombinant plasmids pBE2133:GFP and pBE2133:GFP:MaFT were successfully constructed. Transient expression of MaFT:GFP protein was found in leaves, petiole (cross section), and shoot apical meristem (SAM) of mulberry according to the GFP signal. Moreover, MaFT:GFP mRNA was also detected in leaves and SAM via RT-PCR and qRT-PCR. An efficient transient transformation system could be achieved in mulberry seedlings by syringe using A. tumefaciens GV3101 at the OD600 of 0.5. The movement of MaFT expression from leaves to SAM might trigger the precocious flowering of mulberry.</div>
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