Figure 4.
Overexpression of S100a4, increased phosphorylation of Hes1, and increased activation of Cdk4 and Wee1 infer Notch1 activation. (A) Flow diagram of phosphoproteomic/proteomic experimental setup. (B) Log2 label-free quantification (LFQ) intensity values of all proteins captured (left panel) or phosphopeptides (right panel) across all mice per genotype. (C) Volcano plots representing the difference in log2 LFQ intensity of proteins (left panel) and phosphopeptides (right panel) between Eµ-TCL1 (n = 4) and Eµ-TCL1Akt-C (n = 4) mice. Significant DE proteins/phosphopeptides defined as difference >1 and P < .05 (upregulated in Eµ-TCL1Akt-C = yellow; downregulated = pink). (D) Normalized upstream kinase scores for all 45 kinases with available PhosphoSitePlus kinome data. Bars represent the difference in upstream kinase scores between Eµ-TCL1 (n = 4) and Eµ-TCL1Akt-C (n = 4) (upregulated in Eµ-TCL1Akt-C = yellow; downregulated = pink). (E) Upstream kinase scores from the top significantly upregulated kinases in Eµ-TCL1Akt-C mice. Significant differences between groups assessed by using Student t test, significant proteins/peptides defined as P < .05 as well as difference >1 /<1 for phosphoproteomics/proteomics, whereas for upstream kinase analysis. P < .05 kinases were considered significant. NS, not significant.