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Fig. 9 | BMC Plant Biology

Fig. 9

From: Comparative proteomic and transcriptomic analyses provide new insight into the formation of seed size in castor bean

Fig. 9

Expression patterns of genes related to the formation of seed size in ZB107 and ZB306 during seed development based on qRT-PCR. CYCD1;1, D1-type cyclin (29,168.t000023); SC, serine carboxypeptidase (29,745.t000011); eIF-5A, eukaryotic translation initiation factor 5a (29,687.t000001); ARF2 (29,647.t000040); AUX|IAA, auxin/indole-3-acetic acid (28,179.t000006); BAK1, BRI1-associated receptor kinase 1 (30,190.t000257); BZR1, BR-activated transcription factor BRASSINAZOLE-RESISTANT1 (29,646.t000010); FBA, fructose-bisphosphate aldolase (29,660.t000032); PGK, phosphoglycerate kinase (30,169.t000073); GAPDH, glyceraldehyde 3-phosphate dehydrogenase (30,169.t000047); SAM, S-adenosylmethionine synthetase (30,128.t000431); SRPL13, 60S ribosomal protein L13 (30,071.t000004); SRPL23a, 60S ribosomal protein L23a (28,180.t000008); RPL27a, 60S ribosomal protein L27a (30,147.t000153); and 26S protease regulatory subunit, 29,739.t000101. Expression levels were calculated by the 2−∆∆CT method against the control gene expression. Three biological replicates for each gene were included, and the values of gene expression were shown as mean ± SD. Different lowercase letters indicate significant differences. Data were analyzed with one-way ANOVA and Tukey’s multiple comparison test, p < 0.05

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