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. Author manuscript; available in PMC: 2019 Feb 5.
Published in final edited form as: Cell Rep. 2019 Jan 2;26(1):108–118.e4. doi: 10.1016/j.celrep.2018.12.030

Figure 4. BMI1 Prevents the Upregulation of p53 Signaling and Maintains Large Pre-B Cell Cycling.

Figure 4.

(A) RNA sequencing (RNA-seq) MA (log ratio and mean average) plot of Bmi1+/+ versus Bmi1−/− pro-B cells. Known targets of p53 are depicted in red.

(B) qRT-PCR expression analysis of indicated genes from sorted pro-B cells of indicated mice. Each point represents one animal; the line represents the mean. n = 4 for Bmi1+/+ animals; n = 5 for Bmi1−/− animals.

(C) Frequency of apoptotic (as indicated by annexin V positivity) pro-B cells and pre-B cells of indicated mice. Each point represents one animal; the line represents the mean. n = 5 for each genotype.

(D) Frequency of large pre-B cells present in the pre-B cell compartment of indicated mice. Each point represents one animal; the line represents the mean. n = 6 for each genotype.

(E) FACS plot of developing B cells in the bone marrow of indicated mice. Shown is the frequency of each cell population in the bone marrow of indicated animals. Representative of 3 independent experiments.

(F) Frequency of B220+ cells in the spleen and peripheral blood of indicated mice. Each point represents one animal; the line represents the mean. n = 3 for each genotype.

***p < 0.001, **p < 0.01, *p < 0.05. PB, peripheral blood.

See also Figure S4 and Table S1.