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首页> 外文期刊>Oncogene >Epigenetic mechanisms affect mutant p53 transgene expression in WAP-mutp53 transgenic mice
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Epigenetic mechanisms affect mutant p53 transgene expression in WAP-mutp53 transgenic mice

机译:表观遗传机制影响WAP-mutp53转基因小鼠中突变型p53转基因的表达

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摘要

We describe the construction and phenotypic characterization of 23 whey acidic protein (WAP)-mutp53 transgenic mouse lines. The mutp53-expressing lines showed a mosaic expression pattern for the transgenes, leading to a heterogeneous yet mouse line-specific expression pattern for mutp53 upon induction. Only few lines were obtained, in which the majority of the induced mammary epithelial cells expressed the mutp53 transgene, most of the transgenic lines did not express mutp53, or expressed the transgene in less than 2% of the induced mammary epithelial cells. Hormone requirements for mutp53 transgene expression from the WAP-promoter differed in high and low expressing lines, being low in high expressing lines, and even lower in multiparous mutp53 mice, where persistent expression of the transgene occurred. Repeated induction of mutp53 expression through repeated parturition resulted in the formation of expanding mutp53-expressing foci within the mammary alveolar epithelium. The data suggest that epigenetic mechanisms play a role in modulating the expression of the mutp53 transgene. To support this idea, we crossed a nonexpressing WAP-mutp53 line with a strongly SV40 T-antigen-expressing WAP-T mouse line. In the bitransgenic mice, T-antigen-induced chromatin remodeling led to re-expression of epigenetically silenced mutp53 transgene(s). In these mice, mutp53 expression was much more variable compared to SV40 T-antigen expression, and seemed to depend on the coexpression of SV40 T-antigen. Mutp53 expression in this system thus resembles the situation in many human tumors, where one can observe a heterogeneous expression of mutp53, despite a homogeneous distribution of the p53 mutation in the tumor cells.
机译:我们描述了23乳清酸性蛋白(WAP)-mutp53转基因小鼠品系的构建和表型特征。 mutp53表达系显示了转基因的镶嵌表达模式,诱导后导致mutp53的异质性但小鼠系特异性表达模式。仅获得很少的品系,其中大多数诱导的乳腺上皮细胞表达mutp53转基因,大多数转基因品系不表达mutp53,或在少于2%的诱导的乳腺上皮细胞中表达转基因。来自WAP启动子的mutp53转基因表达的激素需求在高表达和低表达品系中有所不同,在高表达品系中较低,甚至在多胎mutp53小鼠中更低,在后者中转基因持续表达。通过重复分娩来重复诱导mutp53表达,导致在乳腺肺泡上皮内形成扩大的mutp53表达灶。数据表明表观遗传机制在调节mutp53转基因的表达中起作用。为了支持这个想法,我们将不表达WAP mutp53的品系与表达SV40 T抗原的WAP-T小鼠品系进行了杂交。在双转基因小鼠中,T抗原诱导的染色质重塑导致表观遗传沉默mutp53转基因的重新表达。在这些小鼠中,与SV40 T抗原表达相比,mutp53的表达具有更大的可变性,并且似乎取决于SV40 T抗原的共表达。因此,该系统中的mutp53表达类似于许多人类肿瘤中的情况,尽管p53突变在肿瘤细胞中分布均匀,但人们仍可以观察到mutp53的异质表达。

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