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Research ArticleResearch ArticleF
Open Access

SCAMPs Highlight the Developing Cell Plate during Cytokinesis in Tobacco BY-2 Cells

Sheung Kwan Lam, Yi Cai, Stefan Hillmer, David G. Robinson, Liwen Jiang
Sheung Kwan Lam
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Yi Cai
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Stefan Hillmer
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David G. Robinson
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Liwen Jiang
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Published August 2008. DOI: https://doi.org/10.1104/pp.108.119925

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    Figure 1.

    Dynamics of OsSCAMP1-YFP in cell plate formation during cytokinesis in transgenic BY-2 cells. Shown is a continuous series of time-lapse confocal images of OsSCAMP1-YFP signals collected from a single transgenic tobacco BY-2 cell during cell plate formation. Bar = 50 μm. [See online article for color version of this figure.]

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    Figure 2.

    OsSCAMP1-YFP largely colocalizes with internalized endosomal marker FM4-64 in the cell plate during cytokinesis in transgenic BY-2 cells. Tobacco BY-2 cells expressing OsSCAMP1-YFP were allowed to take up FM4-64 for 30 min, followed by confocal image collection on cells in various stages of cytokinesis from A to D. DIC, Differential interference contrast. Bar = 50 μm.

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    Figure 3.

    GONST1-YFP and GFP-BP-80 are largely separated from the internalized endosomal marker FM4-64 during cell plate formation in transgenic BY-2 cells. Tobacco BY-2 cells expressing either the Golgi marker GONST1-YFP (A and B) or the PVC marker GFP-BP-80 (C and D) were allowed to take up FM4-64 under conditions identical to those used for OsSCAMP1-YFP cells, followed by confocal image collection on cells at various stages of cytokinesis. Bar = 50 μm.

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    Figure 4.

    Immunogold EM of SCAMP1 during cell plate formation in transgenic and wild-type BY-2 cells. Ultrathin sections prepared from high-pressure frozen/freeze-substituted synchronized transgenic (A–C) or wild type (D) BY-2 cells were labeled with either anti-GFP antibodies to detect OsSCAMP1-YFP (A–C) or anti-SCAMP1 antibodies to detect the endogenous SCAMP1 proteins (D). Arrows point to gold particles labeling the cell plates; arrowheads indicate examples of TGN labeling or TGN vesicle labeling. G, Golgi apparatus; M, MVB. Bars = 500 nm.

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    Figure 5.

    Immunogold EM of VSRs during cell plate formation in BY-2 cells. Ultrathin sections prepared from high-pressure frozen/freeze-substituted synchronized wild-type BY-2 cells were labeled with anti-VSRat-1 antibodies to detect the endogenous tobacco VSR proteins. Arrows point to gold particles labeling the cell plates. Bars = 500 nm.

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SCAMPs Highlight the Developing Cell Plate during Cytokinesis in Tobacco BY-2 Cells
Sheung Kwan Lam, Yi Cai, Stefan Hillmer, David G. Robinson, Liwen Jiang
Plant Physiology Aug 2008, 147 (4) 1637-1645; DOI: 10.1104/pp.108.119925

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SCAMPs Highlight the Developing Cell Plate during Cytokinesis in Tobacco BY-2 Cells
Sheung Kwan Lam, Yi Cai, Stefan Hillmer, David G. Robinson, Liwen Jiang
Plant Physiology Aug 2008, 147 (4) 1637-1645; DOI: 10.1104/pp.108.119925
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Plant Physiology: 147 (4)
Plant Physiology
Vol. 147, Issue 4
August 2008
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