Fig. 9From: Comparative proteomic and transcriptomic analyses provide new insight into the formation of seed size in castor beanExpression 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 < 0.05Back to article page