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Differential expression of jun and fos genes during differentiation of mouse P19 embryonal carcinoma cells.

机译:在小鼠P19胚胎癌细胞分化过程中jun和fos基因的差异表达。

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摘要

The jun and fos gene families encode DNA binding proteins involved in transcriptional regulation of genes containing a TPA responsive element (TRE). To study their role in gene regulation during early mammalian development, expression and transcription regulatory properties of their gene products were investigated during retinoic acid (RA) induced differentiation of P19 embryonal carcinoma (EC) cells. Our results show, that c-jun is expressed at low but detectable levels in undifferentiated P19 EC cells and at elevated levels in its RA differentiated derivatives, corresponding with increased expression of Jun and TRE binding activity. Jun D is constitutively expressed at constant levels in both undifferentiated and differentiated P19 cells, while jun B and c-fos are not expressed. Addition of TPA to undifferentiated P19 cells does not result in induction of c-jun, jun B and c-fos, while these genes are transiently induced in RA-differentiated P19 cells. In addition, TPA treatment resulted in expression of Fos and Jun protein in RA-differentiated, but not in undifferentiated P19 cells. Addition of TPA to P19 EC cells expressing low levels of TRE binding proteins is neither followed by transcriptional activation of the TRE reporter gene nor by induction of c-jun, previously shown to be autoregulated by its own gene product. By contrast, in P19 cells differentiated by RA that contain elevated levels of TRE binding proteins, TRE dependent transcription is enhanced upon TPA treatment.
机译:jun和fos基因家族编码DNA结合蛋白,参与含有TPA响应元件(TRE)的基因的转录调控。为了研究它们在哺乳动物早期发育过程中在基因调控中的作用,在视黄酸(RA)诱导P19胚胎癌细胞(EC)分化期间研究了其基因产物的表达和转录调控特性。我们的结果表明,c-jun在未分化的P19 EC细胞中以低水平但可检测的水平表达,在其RA分化衍生物中水平升高,与Jun和TRE结合活性的表达增加相对应。 Jun D在未分化和分化的P19细胞中以恒定水平组成性表达,而jun B和c-fos不表达。在未分化的P19细胞中添加TPA不会导致c-jun,jun B和c-fos的诱导,而在RA分化的P19细胞中这些基因是瞬时诱导的。另外,TPA处理导致RA分化的Fos和Jun蛋白表达,而未分化的P19细胞则不表达。在表达低水平的TRE结合蛋白的P19 EC细胞中加入TPA之前,既不激活TRE报告基因的转录激活,也不诱导c-jun的产生,c-jun以前被证明是由其自身的基因产物自动调节的。相比之下,在由RA分化的P19细胞中,TRE结合蛋白水平升高,TPA处理可增强TRE依赖性转录。

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