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. 2017 Sep 26;8:702. doi: 10.1038/s41467-017-00768-1

Fig. 3.

Fig. 3

Sth-independent Thpok repression by Bcl11b in pre-selection DP thymocytes. a Quantitative RT-PCR showing amount of promoter-specific Thpok transcripts in splenic CD4+ T cells and splenic B220+ B lymphocytes. Summary of three measurements. b Quantitative RT-PCR for Thpok-gfp expression in CD4+ T cells from mutant reporter alleles, Thpok gfp:ΔTE and Thpok gfp:ΔPE, lacking the thymic enhancer (TE) or proximal enhancer (PE), respectively. Levels of P1- and P2 promoter-specific transcripts relative to those from the control Thpok gfp allele harboring intact enhancers is shown. One representative of two independent experiments. c Promoter-specific Thpok transcripts in Bcl11b m/m pre-selection DP thymocytes and CD4+ T cells relative to those in control CD4+ T cells. Summary of three measurements. d Histograms showing Thpok-GFP expression from the Thpok gfp:ΔTESPE allele in the indicated cell subsets differentiated in Rag1-deficient recipients from control (dotted line) and Bcl11b m/m (solid line) fetal liver cells. Expression pattern of Thpok gfp is shown as reference (shaded). Schematic structure of the Thpok gfp:ΔTESPE allele is included (upper panel). One representative of two independent experiments. e ATAC-seq tracks at the Thpok locus in CD24hiTCRβloCD4+CD8+ pre-selection thymocytes of 6-week-old Bcl11b +/+ mice, newborn Bcl11b +/fl :Lck-cre, newborn Bcl11b HM/fl :Lck-cre and newborn Bcl11b HM/HM :Lck-cre mice. ATAC-seq results in immature B cells (GSM2123187) is shown as reference. DP thymocyte- and B lymphocyte-specific peaks are marked with blue and red arrowheads, respectively. Position of the P1 promoter is indicated with black arrowhead