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1.
Biol Trace Elem Res ; 144(1-3): 1219-28, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21625916

ABSTRACT

Pineapple (Ananas comosus L. Merr., cv. "Queen") leaf bases were transformed with Agrobacterium tumefaciens strain EHA 105 harboring the pSF and pEFESF plasmids with soybean ferritin cDNA. Four to eight percent of the co-cultivated leaf bases produced multiple shoots 6 weeks after transfer to Murashige and Skoog's medium supplemented with α-naphthalene acetic acid 1.8 mg/l, indole-3-butyric acid 2.0 mg/l, kinetin 2.0 mg/l, cefotaxime 400 mg/l, and kanamycin 50 mg/l. Putatively transformed shoots (1-2 cm) were selected and multiplied on medium of the same composition and elongated shoots (5 cm) were rooted on liquid rooting medium supplemented with cefotaxime 400 mg/l and kanamycin 100 mg/l. The rooted plants were analyzed through PCR, genomic Southern analysis, and reverse transcription PCR. The results clearly confirmed the integration and expression of soybean ferritin gene in the transformed plants. Atomic absorption spectroscopic analysis carried out with six independently transformed lines of pSF and pEFE-SF revealed a maximum of 5.03-fold increase in iron and 2.44-fold increase in zinc accumulation in the leaves of pSF-transformed plants. In pEFE-SF-transformed plants, a 3.65-fold increase in iron and 2.05-fold increase in zinc levels was observed. Few of the transgenic plants were hardened in the greenhouse and are being grown to maturity to determine the enhanced iron and zinc accumulation in the fruits. To the best of our knowledge this is the first report on the transformation of pineapple with soybean ferritin for enhanced accumulation of iron and zinc content in the transgenic plants.


Subject(s)
Ananas/genetics , Ananas/metabolism , Ferritins/genetics , Glycine max/genetics , Iron/metabolism , Plants, Genetically Modified/metabolism , Zinc/metabolism , Agrobacterium tumefaciens/genetics , Blotting, Southern , Culture Media , DNA, Complementary/biosynthesis , DNA, Complementary/genetics , Genetic Vectors , Plant Leaves/chemistry , Plant Leaves/metabolism , Plant Shoots/chemistry , Plant Shoots/metabolism , Polymerase Chain Reaction , Spectrophotometry, Atomic
2.
Planta ; 234(5): 915-32, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21671068

ABSTRACT

Dehydrins are highly hydrophilic proteins involved in playing key adaptive roles in response to abiotic stress conditions having dehydration as a common component. In the present study, a novel banana SK(3)-type dehydrin, MusaDHN-1, was identified and later characterized using transgenic banana plants to investigate its functions in abiotic stress tolerance. Expression profiling in native banana plants demonstrated that MusaDHN-1 was induced in leaves by drought, salinity, cold, oxidative and heavy metal stress as well as by treatment with signalling molecules like abscisic acid, ethylene and methyl jasmonate. Promoter analysis carried out by making a MusaDHN-1 promoter: ß-glucuronidase fusion construct reconfirmed the abiotic stress inducibility of MusaDHN-1. Transgenic banana plants constitutively overexpressing MusaDHN-1 were phenotypically normal and displayed improved tolerance to drought and salt-stress treatments in both in vitro and ex vitro assays. Enhanced accumulation of proline and reduced malondialdehyde levels in drought and salt-stressed MusaDHN-1 overexpressing plants further established their superior performance in stressed conditions. This study is the first to report generation of transgenic banana plants engineered for improved drought and salt-stress tolerance.


Subject(s)
Droughts , Musa/genetics , Plant Proteins/genetics , Salt-Tolerant Plants/genetics , Abscisic Acid/pharmacology , Acetates/pharmacology , Agrobacterium/genetics , Agrobacterium/metabolism , Amino Acid Sequence , Blotting, Southern , Cyclopentanes/pharmacology , Ethylenes/pharmacology , Gene Dosage , Gene Expression Regulation, Plant , Genes, Plant , Genetic Vectors/genetics , Genetic Vectors/metabolism , Malondialdehyde/metabolism , Molecular Sequence Data , Musa/classification , Musa/drug effects , Musa/metabolism , Musa/physiology , Oxylipins/pharmacology , Phylogeny , Plant Leaves/drug effects , Plant Leaves/genetics , Plant Leaves/metabolism , Plant Leaves/physiology , Plant Roots/drug effects , Plant Roots/genetics , Plant Roots/metabolism , Plant Roots/physiology , Plant Somatic Embryogenesis Techniques , Plants, Genetically Modified/drug effects , Plants, Genetically Modified/genetics , Plants, Genetically Modified/metabolism , Plants, Genetically Modified/physiology , Proline/metabolism , Promoter Regions, Genetic , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Salt-Tolerant Plants/drug effects , Salt-Tolerant Plants/metabolism , Salt-Tolerant Plants/physiology , Sequence Alignment , Stress, Physiological
3.
Mol Biol Rep ; 38(6): 4023-35, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21110110

ABSTRACT

WRKY transcription factor proteins play significant roles in plant stress responses. Here, we report the cloning and characterization of a novel WRKY gene, MusaWRKY71 isolated from an edible banana cultivar Musa spp. Karibale Monthan (ABB group). MusaWRKY71, initially identified using in silico approaches from an abiotic stress-related EST library, was later extended towards the 3' end using rapid amplification of cDNA ends technique. The 1299-bp long cDNA of MusaWRKY71 encodes a protein with 280 amino acids and contains a characteristic WRKY domain in the C-terminal half. Although MusaWRKY71 shares good similarity with other monocot WRKY proteins the substantial size difference makes it a unique member of the WRKY family in higher plants. The 918-bp long 5' proximal region determined using thermal asymmetric interlaced-polymerase chain reaction has many putative cis-acting elements and transcription factor binding motifs. Subcellular localization assay of MusaWRKY71 performed using a GFP-fusion platform confirmed its nuclear targeting in transformed banana suspension cells. Importantly, MusaWRKY71 expression in banana plantlets was up-regulated manifold by cold, dehydration, salt, ABA, H2O2, ethylene, salicylic acid and methyl jasmonate treatment indicating its involvement in response to a variety of stress conditions in banana. Further, transient overexpression of MusaWRKY71 in transformed banana cells led to the induction of several genes, homologues of which have been proven to be involved in diverse stress responses in other important plants. The present study is the first report on characterization of a banana stress-related transcription factor using transformed banana cells.


Subject(s)
Genes, Plant/genetics , Musa/cytology , Musa/genetics , Plant Proteins/genetics , Stress, Physiological/genetics , Transcription Factors/genetics , Transformation, Genetic , Base Sequence , Biological Assay , Blotting, Southern , Cell Nucleus/metabolism , Cloning, Molecular , Gene Dosage/genetics , Gene Expression Profiling , Gene Expression Regulation, Plant , Molecular Sequence Data , Phylogeny , Plant Proteins/chemistry , Plant Proteins/metabolism , Plants, Genetically Modified , Protein Transport , Regulatory Sequences, Nucleic Acid/genetics , Reverse Transcriptase Polymerase Chain Reaction , Sequence Alignment , Sequence Analysis, DNA , Transcription Factors/chemistry , Transcription Factors/metabolism
4.
Biol Trace Elem Res ; 142(2): 232-41, 2011 Aug.
Article in English | MEDLINE | ID: mdl-20602178

ABSTRACT

Iron deficiency anemia is one of the serious ailments related to nutrition in the developing countries. Fruit and vegetable crops favor the bioavailability of iron. Banana is consumed as a staple food in the tropics. Iron-fortified bananas provide an effective means of controlling the iron deficiency. Embryogenic cells of banana cv. Rasthali (AAB) were transformed with soybean ferritin cDNA using two different expression cassettes pSF and pEFE-SF to express ferritin. Transgenic nature of the regenerated plants was confirmed by PCR. Transgenic plants were regenerated and analyzed through PCR and PCR-Southern analysis. The expression of ferritin was confirmed by RT-PCR. Iron and zinc levels in the transgenic and control plants were estimated by atomic absorption spectroscopy. A 6.32-fold increase in iron accumulation and a 4.58-fold increase in the zinc levels were noted in the leaves of transgenic plants. Thus, iron- and zinc-fortified bananas could be developed as a functional food to overcome the malnutrition-related iron deficiency. This is the first report on the iron and zinc fortification of banana.


Subject(s)
Ferritins/metabolism , Glycine max/genetics , Iron/metabolism , Musa/metabolism , Plants, Genetically Modified/metabolism , Ferritins/genetics , Musa/genetics , Plants, Genetically Modified/genetics , Reverse Transcriptase Polymerase Chain Reaction , Spectrophotometry, Atomic
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