Gazit B, Panet A, Cedar H
Proc Natl Acad Sci U S A. 1980 Apr;77(4):1787-90. doi: 10.1073/pnas.77.4.1787.
Chicken erythrocyte nuclei have been labeled in the active regions of the chromosome by using the nick translation reaction. In this procedure, accessible areas of the genome are preferentially nicked by the action of pancreatic DNase I and subsequently labeled by using DNA polymerase I from Escherichia coli. These nuclei were employed as a substrate for studying the factors responsible for maintaining the special chromatin conformation of the overall population of active genes. Treatment of nuclei with 0.35 M NaCl resulted in the loss of DNase I sensitivity in the active genes, but this sensitivity could be restored when nuclei were reconstituted with the NaCl eluate. Further purification of the released factors revealed that the HMG (high-mobility group) proteins HMG-14 and HMG-17 are involved in maintaining the conformation of the active regions. These factors are not tissue specific and seem to be involved in the chromosomal structure of most of the active genes.
利用缺口平移反应,已在鸡红细胞核染色体的活性区域进行了标记。在此过程中,基因组的可及区域优先被胰脱氧核糖核酸酶I作用产生缺口,随后用来自大肠杆菌的DNA聚合酶I进行标记。这些细胞核被用作研究负责维持活性基因总体特殊染色质构象的因子的底物。用0.35M氯化钠处理细胞核导致活性基因中脱氧核糖核酸酶I敏感性丧失,但当用氯化钠洗脱液重构细胞核时,这种敏感性可以恢复。对释放因子的进一步纯化表明,高迁移率族(HMG)蛋白HMG - 14和HMG - 17参与维持活性区域的构象。这些因子不是组织特异性的,似乎参与了大多数活性基因的染色体结构。