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. 2014 Mar 22;65(9):2351–2363. doi: 10.1093/jxb/eru114

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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. 3. — Expression of genes associated with sugar metabolism in WT and transgenic SlAREB1 fruits. qRT-PCR analysis of genes encoding the tomato vacuolar invertase 1 (TIV1), cell wall invertase (LIN5), sucrose synthase 2 (SUS2), sucrose synthase 3 (SUS3), sucrose phosphate synthase (SPS), ADP-glucose pyrophosphorylase (AGPase), phosphoenolpyruvate carboxylase (PEPC), aconitate hydratase (ACOH), α-keto acid dehydrogenase, branched chain (E2b), succinate dehydrogenase 1 (SDH1), fumarase (FUM), and mitochondrial malate dehydrogenase (mMDH) in pericarp of immature green (IG) and ripe red (RR) fruits of wild-type (WT), AS (A3, A4, light hatched bars), and OE (S2, S3, dark hatched bars) lines. Bars indicate mean relative expression ±SE (n=3) normalized against EF1α. Asterisks indicate significant differences in transcript abundance compared with the WT (P≤0.05).