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. 2022 Jan 29;11(2):218. doi: 10.3390/biology11020218

Table 1.

Presence of the Trp53R270H mutant allele mediates alterations in the expression levels of validated transcriptional targets of wildtype p53. The expression of 16 genes that are known transcriptional targets of wildtype p53 was impacted by the presence of the Trp53R270H mutant allele. It is noteworthy that allele dosage effects were observed for some genes; Bax, Ccng1, Cdkn1a, Gdf15, Mdm2. Data shown are fragments per kilobase of exon model per million mapped reads (FPKM).

Gene p Value (ANOVA) Trp53+/+
(Mouse #1)
Trp53+/+
(Mouse #2)
Trp53+/R270H
(Mouse #1)
Trp53+/R270H
(Mouse #2)
Trp53R270H/R270H
(Mouse #1)
Trp53R270H/R270H
(Mouse #2)
Acta1 0.03226382 459.72382 723.69403 1295.8693 1305.2902 1532.4598 1335.5698
Bax 0.00234206 92.46413 90.38328 67.5547 58.88641 26.7726 21.443594
Bbc3 0.00355776 22.755802 18.623598 13.3205 11.639098 6.8682103 6.6584005
Cav1 0.00357872 82.86131 84.6536 83.98589 89.3961 113.60498 110.93498
Ccng1 0.00381259 216.86192 178.55894 80.588196 99.719315 50.149597 54.22179
Cdkn1a 2.50 × 10−5 108.96001 100.64 40.4964 41.430794 6.70245 6.1654506
Ddit4 0.04823983 57.755894 79.54468 45.9636 41.706512 35.910603 27.632603
Gdf15 0.01252794 30.834797 61.762997 22.0756 10.823901 2.20235 2.4798
Hsp90ab1 0.03196126 669.3211 686.84717 753.2858 651.8237 433.094 504.98203
Mdm2 0.00440876 53.018593 45.430508 26.794598 29.479399 18.8087 21.066896
Nos3 0.04553094 1.25112 1.57297 2.18129 2.02219 2.01661 2.03199
Ppm1j 0.03864105 1.14598 2.0899 4.44729 4.88169 4.1659994 3.9569898
Prkab1 0.03862554 65.31939 59.280407 60.98009 58.167007 46.9706 50.6644
Ptk2b 0.04042444 15.3253975 15.081601 14.640602 12.964701 11.9638 11.0372
Tap1 0.04544611 22.922 17.592104 14.591501 12.070802 11.3092985 10.970899
Tnfrsf10b 0.00248734 6.25948 5.06814 1.88841 2.3068597 1.18625 1.04909

heterozygous (Trp53+/R270H) and/or or homozygous mice (Trp53R270H/R270H). A dose-dependent effect was observed for Mgmt. The expression of 4 genes which are associated with prostate cancer incidence and/or disease progression (Cdkn1a, Kras, Raf1, and Cav1) were impacted by the presence of the Trp53R270H allele. A gene dosage effect was observed for 1 of these, Cdkn1a. Data shown are fragments per kilobase of exon model per million mapped reads (FPKM).