Baron M H, Maniatis T
Cell. 1986 Aug 15;46(4):591-602. doi: 10.1016/0092-8674(86)90885-8.
Interspecific heterokaryons were formed by fusing adult mouse erythroleukemia (MEL) cells and human embryonic/fetal erythroid (K562) cells with each other, or with a variety of mouse and human nonerythroid cell types. Analysis of total cellular RNA isolated 24 hr after fusion revealed that normally inactive globin genes can be activated in these "transient" heterokaryons, in which the nuclei do not fuse. In general, the types of globin genes expressed in the donor erythroid cell are activated in the nucleus of the recipient cell. Therefore, erythroid cells contain transacting regulatory factors that are capable of activating the expression of globin genes in a stage- and tissue-specific manner. These observations also indicate that globin genes are not irreversibly repressed in differentiated cells and that their expression can be rapidly reprogrammed in the presence of the appropriate regulatory factors.
通过将成年小鼠红白血病(MEL)细胞与人胚胎/胎儿红系(K562)细胞相互融合,或与多种小鼠和人类非红系细胞类型融合,形成了种间异核体。对融合后24小时分离的总细胞RNA进行分析发现,在这些细胞核不融合的“瞬时”异核体中,正常情况下无活性的珠蛋白基因可以被激活。一般来说,供体红系细胞中表达的珠蛋白基因类型在受体细胞的细胞核中被激活。因此,红系细胞含有能够以阶段和组织特异性方式激活珠蛋白基因表达的反式作用调节因子。这些观察结果还表明,珠蛋白基因在分化细胞中并非被不可逆地抑制,并且在存在适当调节因子的情况下,它们的表达可以迅速重新编程。