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. 2013 Sep 4;64(14):4403–4419. doi: 10.1093/jxb/ert251

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© The Author 2013. 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. 8. — Schematic representation of GA metabolism in grapevine inflorescence. Schematic overview of GA₁ and GA₄ metabolism in inflorescences at anthesis (left) and after 7 d (right side). Squares represent detected GA₁ and GA₄, and their dimension is proportional to their concentrations. Circles represent genes whose transcripts were detected (full-length cDNA sequences) in inflorescences. Their dimension at anthesis is proportional to their transcript abundance, as determined by RNA-seq; whereas at 7 d it is proportional to their expression level as extrapolated by qRT–PCR data (only significant changes are reported, P < 0.05). For each gene, the flower organ in which it is predominant is indicated: CAL, calyptra; S/P, stamen and/or pollen; CAR, carpel; ALL, the transcript is distributed in all flower organs. (This figure is available in colour at JXB online.)