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. 2014 May 6;65(12):3215–3223. doi: 10.1093/jxb/eru179

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© The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 6. — Interactor of the MYB82 protein. (A) Interaction of MYB82 with GL3 in yeast; interaction was indicated by the ability of cells to grow on synthetic dropout medium lacking Leu/Trp/His/Ade and containing 5mM 3AT; full-length MYB (MYB82 and GL1), N-terminal truncated MYB (nMYB), and C-terminal truncated MYB (cMYB) were cloned into pGBKT7; full-length GL3 was cloned into pGADT7. (B) Interaction of MYB82 with GL3 in plant cells; fluorescence was observed in nuclear compartments of Nicotiana benthamiana leaf epidermal cells, resulting from complementation of the N-terminal portion of YFP fused to MYB82 (MYB82-nYFP) with the C-terminal portion of YFP fused to GL3 (GL3-cYFP).