Guttenbach M, Schmid M
Institut für Humangenetik, Biozentrum, Am Hubland, Würzburg, FRG.
Exp Cell Res. 1994 Mar;211(1):127-32. doi: 10.1006/excr.1994.1068.
Lymphocyte cultures of a male proband were treated with 5-azacytidine. This cytidine analogue induces distinct undercondensation in the heterochromatic regions of chromosomes 1, 9, 15, 16, and Y and increases the frequency of micronuclei formation. In order to analyze the chromosomal content of these micronuclei, in situ hybridizations with biotinylated probes specific for chromosomes 1, 9, 15, 16, and Y were performed. Probes for chromosomes 11, 17, and X were used as controls. Each of 5000 hybridized cell nuclei was scored for associated micronuclei, and signal distribution was documented. In preparations hybridized with probes detecting the 5-azacytidine-sensitive chromosomes a significant fraction of micronuclei showed hybridizations. In contrast, micronuclei in preparations probed for chromosomes 11, 17, and X lacked hybridization signals. The results suggest that in 5-azacytidine-treated cultures the 5-azacytidine-sensitive chromosomes are preferentially excluded into the micronuclei.
对一名男性先证者的淋巴细胞培养物用5-氮杂胞苷进行处理。这种胞苷类似物会在1号、9号、15号、16号染色体以及Y染色体的异染色质区域诱导明显的凝缩不足,并增加微核形成的频率。为了分析这些微核的染色体组成,使用了针对1号、9号、15号、16号染色体以及Y染色体的生物素化探针进行原位杂交。使用针对11号、17号染色体以及X染色体的探针作为对照。对5000个杂交细胞核中的每一个进行相关微核的计数,并记录信号分布情况。在用检测对5-氮杂胞苷敏感染色体的探针杂交的标本中,相当一部分微核显示出杂交信号。相比之下,用针对11号、17号染色体以及X染色体的探针检测的标本中的微核缺乏杂交信号。结果表明,在经5-氮杂胞苷处理的培养物中,对5-氮杂胞苷敏感的染色体优先被排除到微核中。