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. 2017 May 2;68(11):2717–2729. doi: 10.1093/jxb/erx147

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© The Author 2017. 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/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 2. — Expression of the candidate regulatory genes during pod development. (A) Unigene11350_Z. (B) Unigene73512_Z. (C) Unigene23339_Z. (D) Unigene28049_Z. (E) Unigene20212_Z. (F) Unigene13252_Z. (G) Unigene104457_Z. (H) Unigene28374_Z. (I) Unigene75451_Z. (J) Unigene6436_Z. (K) Unigene35090_Z. The transcription factor (TF) families are given in parentheses after the Unigenes. The unfertilized flower buds and different developing pod stages as indicated were harvested from G. max (SN14) and G. soja (ZYD00006). Actin (Glyma18g52780) is used as the internal control in qRT–PCR. The average relative expression and the SD are presented (n=3). Unigenes with a similar expression pattern are in the same background color. The blue column represents gene expression in SN14, while the red column indicates gene expression in ZYD00006. Asterisks indicate significance using Student’s t-test (*P<0.05; **P<0.01) when gene expression in SN14 was compared with that in ZYD00006.