Marcaud L, Reynaud C A, Therwath A, Scherrer K
Nucleic Acids Res. 1981 Apr 24;9(8):1841-51. doi: 10.1093/nar/9.8.1841.
Having previously found a reduced transcription of globin genes and an abortive processing of the already transcribed globin pre-mRNA in Avian Erythroblastosis Virus (AEV) transformed cells (1), we compared the genomic DNA of these cells with that of normal chicken erythroblasts, using 32-P-labelled cDNA probes specific for the beta, alpha A and alpha D globin sequences. Restriction endonuclease digestion, electrophoresis of digests in agarose gels, Southern blotting and hybridization were carried out. Our results show that the overall genome organization is not disturbed in the immediate neighbourhood of the adult globin genes; the observed restriction fragments are identical for both DNAs after EcoRI, HindIII, BamHI and XbaI digestion, using the beta, alpha A and alpha D globin cDNA probes. However, we observe specific modifications at some methylation sites in the beta, beta-like and alpha D regions: after HpaII or MspI digestion in the alpha D region and after HhaI digestion in the beta and beta-like region, heavier bands appear in the transformed cell DNA in addition to the ones observed in normal DNA. This implies that, at some specific sites, the transformed cell DNA is more methylated than the normal erythroblast DNA. The possible significance of this observation is discussed.
我们之前发现,在禽成红细胞增多症病毒(AEV)转化细胞中,珠蛋白基因的转录减少,且已转录的珠蛋白前体mRNA的加工过程中止(1)。我们用对β、αA和αD珠蛋白序列有特异性的32-P标记cDNA探针,将这些细胞的基因组DNA与正常鸡成红细胞的基因组DNA进行了比较。进行了限制性内切酶消化、消化产物在琼脂糖凝胶中的电泳、Southern印迹和杂交。我们的结果表明,在成人珠蛋白基因的紧邻区域,整体基因组组织未受干扰;使用β、αA和αD珠蛋白cDNA探针,经EcoRI、HindIII、BamHI和XbaI消化后,两种DNA观察到的限制性片段相同。然而,我们在β、β样和αD区域的一些甲基化位点观察到了特异性修饰:在αD区域经HpaII或MspI消化后,以及在β和β样区域经HhaI消化后,除了在正常DNA中观察到的条带外,转化细胞DNA中还出现了更重的条带。这意味着,在某些特定位点,转化细胞DNA比正常成红细胞DNA甲基化程度更高。本文讨论了这一观察结果可能的意义。