Coveney J, Scott G, King R, Burke D C, Skup D
Biochem Biophys Res Commun. 1984 May 31;121(1):290-6. doi: 10.1016/0006-291x(84)90721-6.
DNase I sensitivity was used to investigate the chromatin conformation of the interferon beta gene during differentiation of the mouse teratocarcinoma cell line PC13 . These cells do not produce interferon upon viral induction in their undifferentiated state, but do so on differentiation from stem cells to endoderm. Only in induced differentiated cells were the interferon beta genes digested by DNase I. A similar effect was seen in a line of human cells ( MG63 ) upon induction. We conclude that it is induction of interferon production that brings about the change in the DNase I sensitivity of these genes, rather than differentiation.
利用DNA酶I敏感性来研究小鼠畸胎瘤细胞系PC13分化过程中干扰素β基因的染色质构象。这些细胞在未分化状态下经病毒诱导不产生干扰素,但从干细胞分化为内胚层时则会产生。只有在诱导分化的细胞中,DNA酶I才能消化干扰素β基因。在人细胞系(MG63)诱导后也观察到了类似的效应。我们得出结论,是干扰素产生的诱导导致了这些基因对DNA酶I敏感性的变化,而不是分化。