Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens

We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the...

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Veröffentlicht in:In vitro cellular & developmental biology. Plant 2013-04, Vol.49 (2), p.114-128
Hauptverfasser: Pal, Ajantaa, Swain, Swasti S, Das, Anath B, Mukherjee, Arup K, Chand, Pradeep K
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container_title In vitro cellular & developmental biology. Plant
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creator Pal, Ajantaa
Swain, Swasti S
Das, Anath B
Mukherjee, Arup K
Chand, Pradeep K
description We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene.
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Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/s11627-013-9489-9</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Agrobacterium ; Agrobacterium radiobacter ; Amaranth ; Amaranthus tricolor ; Antibiotics ; Aqueous solutions ; beta-glucuronidase ; Biomedical and Life Sciences ; BIOTECHNOLOGY ; Cell Biology ; Chlorophyll ; Cultivation ; Developmental Biology ; DNA ; Drinking water ; Epicotyls ; explants ; Genes ; genetic transformation ; Genetically altered foods ; germ cells ; Infections ; kanamycin ; kanamycin kinase ; leaf protein ; Life Sciences ; Membrane filters ; Microbiology ; Plant Breeding/Biotechnology ; Plant cells ; Plant Genetics and Genomics ; Plant Sciences ; Plants ; plasmids ; polymerase chain reaction ; progeny ; Seedlings ; Seeds ; Shoots ; Southern blotting ; Transgenes ; Transgenic plants ; vegetable crops ; Vegetables</subject><ispartof>In vitro cellular &amp; developmental biology. 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Plant</title><addtitle>In Vitro Cell.Dev.Biol.-Plant</addtitle><description>We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. 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Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pal, Ajantaa</au><au>Swain, Swasti S</au><au>Das, Anath B</au><au>Mukherjee, Arup K</au><au>Chand, Pradeep K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens</atitle><jtitle>In vitro cellular &amp; developmental biology. Plant</jtitle><stitle>In Vitro Cell.Dev.Biol.-Plant</stitle><date>2013-04-01</date><risdate>2013</risdate><volume>49</volume><issue>2</issue><spage>114</spage><epage>128</epage><pages>114-128</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><doi>10.1007/s11627-013-9489-9</doi><tpages>15</tpages></addata></record>
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subjects Agrobacterium
Agrobacterium radiobacter
Amaranth
Amaranthus tricolor
Antibiotics
Aqueous solutions
beta-glucuronidase
Biomedical and Life Sciences
BIOTECHNOLOGY
Cell Biology
Chlorophyll
Cultivation
Developmental Biology
DNA
Drinking water
Epicotyls
explants
Genes
genetic transformation
Genetically altered foods
germ cells
Infections
kanamycin
kanamycin kinase
leaf protein
Life Sciences
Membrane filters
Microbiology
Plant Breeding/Biotechnology
Plant cells
Plant Genetics and Genomics
Plant Sciences
Plants
plasmids
polymerase chain reaction
progeny
Seedlings
Seeds
Shoots
Southern blotting
Transgenes
Transgenic plants
vegetable crops
Vegetables
title Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens
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