Torchia B S, Migeon B R
Center for Medical Genetics, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-3914, USA.
Somat Cell Mol Genet. 1995 Sep;21(5):327-33. doi: 10.1007/BF02257467.
We have recently reported results of DNA replication analysis of three X-linked loci (FRAXA, F8C and XIST) on the X chromosomes in male and female fibroblasts using fluorescence in situ hybridization (FISH) (1). Although our findings that XIST replicates later on the active X than on the inactive X are similar to those of Boggs & Chinault (2) based on a FISH assay in female lymphoblasts, they are the opposite of observations recently reported by Hansen et al. (3) using a different technique. Because our conclusions about the inactive X were deduced from the behavior of the active X in male cells, we reexamined the time when these loci replicate on the human inactive X chromosome isolated from its homolog in somatic cell hybrids. We also studied the same chromosome as an active X in related hybrids. The results provide direct evidence that the expressed XIST locus on the inactive X replicates earlier than its repressed homolog on the active X and earlier than the FRAXA locus which is repressed on this chromosome. The silent XIST locus on the active X replicates late along with F8C which is also not transcribed in these cells. Possible reasons for the different results obtained by Hansen et al. (3) are discussed.
我们最近报道了利用荧光原位杂交(FISH)技术对男性和女性成纤维细胞X染色体上三个X连锁基因座(FRAXA、F8C和XIST)进行DNA复制分析的结果(1)。尽管我们发现XIST在活性X染色体上的复制晚于非活性X染色体,这一结果与Boggs和Chinault基于女性淋巴母细胞FISH分析得出的结果相似(2),但却与Hansen等人最近使用不同技术报道的观察结果相反(3)。由于我们关于非活性X染色体的结论是从男性细胞中活性X染色体的行为推断出来的,因此我们重新研究了这些基因座在从体细胞杂种中的同源染色体分离出来的人类非活性X染色体上进行复制的时间。我们还在相关杂种中研究了作为活性X染色体的同一条染色体。结果提供了直接证据,表明非活性X染色体上表达的XIST基因座比活性X染色体上受抑制的同源基因座复制得早,且比该染色体上受抑制的FRAXA基因座复制得早。活性X染色体上沉默的XIST基因座与同样在这些细胞中不转录的F8C一起复制得晚。文中讨论了Hansen等人(3)获得不同结果的可能原因。