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Fig. 11 | BMC Plant Biology

Fig. 11

From: Physiological and protein profiling analysis provides insight into the underlying molecular mechanism of potato tuber development regulated by jasmonic acid in vitro

Fig. 11

The JA-responsive DEPs involved in protein biosynthesis, degradation and assembly during tuber development in vitro. The heat-map presented the expression change of these DEPs. The significance of t-test was presented by “*” (p < 0.05). The green band indicated the corrected p-value (Padj < 0.05, one-way ANOVA analysis of variance followed by Bonferroni correction for multiple comparison) was mapped as an annotation of heatmap. BIP, luminal binding protein; CNX, calnexin; GRP94, glucose-regulated protein 94; EIF2, eukaryotic translation initiation factor 2; EIF6, eukaryotic translation initiation factor 6; HnRNP A1, heterogeneous nuclear ribonucleoprotein A1; HnRNP G, heterogeneous nuclear ribonucleoprotein G; HSP20, heat shock protein 20; HSP90A, heat shock protein 90A; HYOU1, hypoxia up-regulated protein 1; NOP58, MAR-binding protein NOP58; PSMB6, proteasome subunit β type 6; RAN, GTP-binding nuclear protein; RPN1, proteasome subunit RPN1; RPT2, proteasome subunit RPT2; RP-L3e, ribosomal protein L3e; RP-L7Ae, ribosomal protein L7Ae; RP-L10Ae, ribosomal protein L10Ae; RP-L17e, ribosomal protein L17e; RP-L18e, ribosomal protein L18e; RP-S2e, ribosomal protein S2e; RP-S23e, ribosomal protein S23e; RP-S24e, ribosomal protein S24e; SF3b3, splicing factor 3b subunit 3; UAP56, DEAD-box ATP-dependent RNA helicases; SAR1, secretion-associated RAS superfamily 1; DKC1, Dyskerin 1

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