Pratt M A, Langston A W, Gudas L J, McBurney M W
Department of Medicine, University of Ottawa, Ontario, Canada.
Differentiation. 1993 Jun;53(2):105-13. doi: 10.1111/j.1432-0436.1993.tb00650.x.
Murine P19 embryonal carcinoma cells irreversibly differentiate into neuroectoderm following brief exposure to retinoic acid (RA). We compared the expression of RA-responsive genes in P19 cells and in a mutant cell line from mouse, RAC65, which fails to differentiate in RA. Some RA-responsive genes were normally regulated by RA in RAC65 cells while others were not. Amongst the latter were Oct-3 and PEA-3, whose transcripts rapidly disappeared following RA treatment of P19 cells but which were lost only slowly and incompletely from RAC65 cells. Expression of the Hox 1.6, 1.4, and 1.3 transcripts was induced by RA in P19 cells but not in RAC65 cells. Nuclear run-on and transfection assays indicated that transcription of the Hox 1.6 gene was regulated by a previously identified [26] DNA sequence located 3' of the Hox 1.6 gene, probably through interaction with the alpha RA receptor (RAR alpha). Results of nuclear run-on analysis suggested that expression of the Hox 1.6 gene may also be regulated post-transcriptionally. Constitutive expression of Hox 1.6 from a heterologous promoter did not induce differentiation indicating that expression of this gene is insufficient to initiate the cascade of events that culminates in cell differentiation.
小鼠P19胚胎癌细胞在短暂暴露于视黄酸(RA)后不可逆地分化为神经外胚层。我们比较了P19细胞和来自小鼠的突变细胞系RAC65中RA反应基因的表达,RAC65在RA中不能分化。一些RA反应基因在RAC65细胞中正常受RA调控,而另一些则不然。后者包括Oct-3和PEA-3,其转录本在RA处理P19细胞后迅速消失,但在RAC65细胞中仅缓慢且不完全丢失。Hox 1.6、1.4和1.3转录本的表达在P19细胞中由RA诱导,但在RAC65细胞中未被诱导。细胞核连续标记和转染试验表明,Hox 1.6基因的转录受位于Hox 1.6基因3'端的先前鉴定的[26]DNA序列调控,可能是通过与α视黄酸受体(RARα)相互作用。细胞核连续标记分析结果表明,Hox 1.6基因的表达也可能在转录后受到调控。从异源启动子组成型表达Hox 1.6并未诱导分化,表明该基因的表达不足以启动最终导致细胞分化的一系列事件。