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. 2016 Sep 1;67(18):5557–5569. doi: 10.1093/jxb/erw324

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© The Author 2016. 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. 1. — Expression profile of two rice phosphoglucomutase genes (A) and subcellular localization of OspPGM-GFP protein (B). (A) RT-PCR analysis of OspPGM (LOC_Os03g50480) and OscPGM (LOC_Os10g11140) at different stages of pollen development. OsUBQ5 was used as the PCR control. (B) Chloroplast localization of OspPGM–GFP fusion protein in maize protoplasts. A full-length OspPGM cDNA was fused in-frame to GFP and expressed under the control of the CaMV35S promoter. The fluorescent GFP signal, chloroplast autofluorescence, light microscope view, and a merged image are shown from left to right.