Siebenlist U, Hennighausen L, Battey J, Leder P
Cell. 1984 Jun;37(2):381-91. doi: 10.1016/0092-8674(84)90368-4.
A chromosomal myc gene displays one of three patterns of activity depending upon the arrangement of the gene and its allelic partner. In nonmalignant B cells both myc alleles are normally expressed. In Burkitt lymphoma cells carrying both a translocated and a nontranslocated myc allele, the translocated allele is inappropriately expressed, while the nontranslocated allele is virtually inactive. Here we examine the chromatin structure of these genes using DNAase I hypersensitivity in nonmalignant lymphoblastoid cells and in the Burkitt lymphoma, BL31 . Three hypersensitivity patterns emerge that correlate with the state of the gene and reveal sites associated with putative regulatory structures. One region is associated with the two myc promoters, one with a specific nuclear protein binding site, and one--which is markedly enhanced in the inactive germline gene in the Burkitt cell--with a putative negative control region. The perturbation of the normal pattern in this particular Burkitt cell may be due to the action of an immunoglobulin enhancer.
一个染色体上的myc基因根据该基因及其等位基因伙伴的排列呈现出三种活性模式之一。在非恶性B细胞中,两个myc等位基因通常都有表达。在携带一个易位和一个非易位myc等位基因的伯基特淋巴瘤细胞中,易位的等位基因异常表达,而非易位的等位基因实际上无活性。在此,我们利用DNA酶I超敏反应研究了非恶性淋巴母细胞和伯基特淋巴瘤BL31中这些基因的染色质结构。出现了三种超敏反应模式,它们与基因状态相关,并揭示了与假定调控结构相关的位点。一个区域与两个myc启动子相关,一个与特定的核蛋白结合位点相关,还有一个——在伯基特细胞中无活性的种系基因中显著增强——与一个假定的负调控区域相关。在这个特定的伯基特细胞中正常模式的扰动可能是由于免疫球蛋白增强子的作用。