Takagi N, Sugawara O, Sasaki M
Chromosoma. 1982;85(2):275-86. doi: 10.1007/BF00294971.
We have made a detailed study of the X-chromosome replication pattern during the period when X-inactivation is occurring in the mouse embryo. Our observations show unequivocal regionalization of the embryo with respect to the temporal X-chromosome. The switch from isocyclic to allocyclic replication occurs in the embryonic ectoderm at approximately 6 days of development and is random with respect to parental origin of the X-chromosome. In the extra-embryonic tissues, however, the switch to allocyclic replication has apparently occurred prior to 5.3 days of development and almost exclusively involves the paternally-derived X-chromosome. Since these findings are consistent with results obtained in biochemical studies of X-chromosome activity in female embryos, we conclude that there is a close temporal relationship between the cytogenetic and biochemical manifestations of the X-inactivation process. In addition, we have observed a pattern of early paternal X-chromosome replication, transitory in some cases, that is unique to extra-embryonic tissues. These results suggest that there may be some differences in the mechanism by which X-inactivation occurs in the extra-embryonic tissues as compared with the embryonic ectoderm.
我们对小鼠胚胎发生X染色体失活期间的X染色体复制模式进行了详细研究。我们的观察结果明确显示,胚胎在X染色体时间方面存在区域化现象。从等周期复制到异周期复制的转变大约在发育6天时发生于胚胎外胚层,且与X染色体的亲本来源无关。然而,在胚外组织中,向异周期复制的转变显然在发育5.3天之前就已发生,并且几乎只涉及父源X染色体。由于这些发现与在雌性胚胎X染色体活性的生化研究中获得的结果一致,我们得出结论,X染色体失活过程的细胞遗传学和生化表现之间存在密切的时间关系。此外,我们观察到一种早期父源X染色体复制模式,在某些情况下是短暂的,这是胚外组织所特有的。这些结果表明,与胚胎外胚层相比,X染色体失活在胚外组织中的发生机制可能存在一些差异。