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. 2018 Sep 21;9:3855. doi: 10.1038/s41467-018-06249-3

Fig. 4.

Fig. 4

beta cell BCL11A regulates multiple pathways associated with human insulin secretion. a Workflow employed to generate RNA-seq libraries. b Schematics of lentiviral construct used to knockdown BCL11A expression. c FACS scheme used to obtain GFP expressing beta cells. d BCL11A mRNA expression in GFP expressing beta cells post FACS, control (white bar) or BCL11A-kd (black bar) (n = 4). e Pearson correlation coefficient matrix of all RNA-seq samples used in this study. f Fold transcript levels of genes critical for the maintenance of beta cell identity and function (n = 4). g GO terms enrichment in genes mis-regulated in beta cells post-BCL11A knockdown. h Fold transcript levels of genes significantly altered in beta cells post-BCL11A knockdown (n = 4). See also Supplementary Figure 4. The data presented as mean, error bars represent the standard error, and two-tailed t tests were used to generate p values. *p < 0.05, **p < 0.01