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Research ArticleDEVELOPMENT AND GROWTH REGULATION
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Controlled Cytokinin Production in Transgenic Tobacco Using a Copper-Inducible Promoter

Marian Jane McKenzie, Vadim Mett, Paul Hugh Stewart Reynolds, Paula Elizabeth Jameson
Marian Jane McKenzie
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Vadim Mett
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Paul Hugh Stewart Reynolds
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Paula Elizabeth Jameson
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Published March 1998. DOI: https://doi.org/10.1104/pp.116.3.969

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    Fig. 1.

    Morphological comparison of tobacco lines ID8, ID9, and IR19. Left, Morphologically normal line ID8 21 d after subculture. Top right, Morphologically aberrant line ID9 21 d after subculture. Bottom right, Morphologically aberrant line IR19 21 d after subculture. The plants were grown in tissue culture on solid Murashige-Skoog medium containing 150 mg L−1kanamycin but no CuSO4.

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    Fig. 2.

    Comparison of leaf senescence in Cu-GUS and Cu-ipt tobacco transformants following treatment with 50 μm CuSO4. Cu-GUS (left) and Cu-ipt (right) plants growing in vitro following 97 d of treatment with 50 μm CuSO4.

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    Fig. 3.

    Comparison of growth patterns in Cu-GUS and Cu-ipt tobacco transformants following treatment with Cu. Left, Representative plant from Cu-GUS line GD11 following 30 d of treatment with Cu. Middle and right, Representative plants from Cu-ipt line ID8 following 30 d of treatment with Cu.

Tables

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    Table I.

    Cytokinins detected in the leaf tissue of Cu-ipt tobacco lines ID8 and ID9 under noninductive conditions

    CytokininID8ID9
    pmol g−1fresh wt
    ZRnd-a 134.4
    DZRTrace-b Trace
    iPATrace9.6
    ZOGTrace96.4
    ZROGnd46.9
    ZNTTrace28.0
    TotalTrace315.3

    Values have been corrected for losses during purification and for differential cross-reactivity of the antibodies. The detection limit for ZR with clone 16 was 0.6 pmol and for iPA with clone 12 it was 0.8 pmol.

      • ↵F0-a nd, Not detected.

      • ↵F0-b Trace, Quantities detected were below the limit for accurate quantification of 1 pmol g−1 fresh weight.

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      Table II.

      Comparison of the cytokinins detected in the leaf tissue of Cu-ipt tobacco line ID13 following in vitro treatment with water (−CuSO4) or Cu (+CuSO4).

      Cytokinin−CuSO4+CuSO4
      pmol g−1 fresh wt
      Znd1-a 27.5
      DZRnd52.2
      iPTrace1-b 40.5
      ZOGnd11.8
      TotalTrace132.0

      Values have been corrected for losses during purification and for differential cross-reactivity of the antibodies. The detection limit for ZR with clone 16 was 0.6 pmol and for iPA with clone 12 it was 0.8 pmol.

        • ↵F1-a nd, Not detected.

        • ↵F1-b Trace, Quantities detected were below the limit for accurate quantification of 1 pmol g−1 fresh weight.

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        Table III.

        Growth patterns of Cu-GUS and Cu-ipt tobacco from the in vivo experiment following 30 d of exposure to Cu

        StrainWhole PlantLateral BudsNode No.2-a
        HeightLeavesNo.LengthLeaves
        cmno.cmno.
        Cu-GUS14.5  (0.76)a8.6  (0.47)a1.2  (0.25)a4.5  (0.64)a2.1  (0.17)a4.1  (0.57)a
        Cu-ipt 14.9  (0.62)a11.8  (0.39)b3.3  (0.21)b7.0  (0.52)b2.7  (0.12)b5.6  (0.41)a
        P > 0.05P < 0.0001P < 0.0001P = 0.0009P = 0.0083P > 0.05

        Data presented are the estimates of the least-squares means of the morphological characteristics measured. ses are in parentheses. Those figures in each column followed by a different letter are significantly different at P ≤ 0.05.

          • ↵F2-a The node from which axillary buds were released (nodes were numbered upward from the base).

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        Controlled Cytokinin Production in Transgenic Tobacco Using a Copper-Inducible Promoter
        Marian Jane McKenzie, Vadim Mett, Paul Hugh Stewart Reynolds, Paula Elizabeth Jameson
        Plant Physiology Mar 1998, 116 (3) 969-977; DOI: 10.1104/pp.116.3.969

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        Controlled Cytokinin Production in Transgenic Tobacco Using a Copper-Inducible Promoter
        Marian Jane McKenzie, Vadim Mett, Paul Hugh Stewart Reynolds, Paula Elizabeth Jameson
        Plant Physiology Mar 1998, 116 (3) 969-977; DOI: 10.1104/pp.116.3.969
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        Plant Physiology: 116 (3)
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        Mar 1998
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