European Molecular Biology Laboratory-Centre for Genomic Regulation (EMBL-CRG) Systems Biology Unit, CRG, the Barcelona Institute of Science and Technology, 08003 Barcelona, Spain.
Universitat Pompeu Fabra, 08003 Barcelona, Spain.
Sci Adv. 2017 Aug 16;3(8):e1701143. doi: 10.1126/sciadv.1701143. eCollection 2017 Aug.
Impaired DNA replication is a hallmark of cancer and a cause of genomic instability. We report that, in addition to causing genetic change, impaired DNA replication during embryonic development can have major epigenetic consequences for a genome. In a genome-wide screen, we identified impaired DNA replication as a cause of increased expression from a repressed transgene in . The acquired expression state behaved as an "epiallele," being inherited for multiple generations before fully resetting. Derepression was not restricted to the transgene but was caused by a global reduction in heterochromatin-associated histone modifications due to the impaired retention of modified histones on DNA during replication in the early embryo. Impaired DNA replication during development can therefore globally derepress chromatin, creating new intergenerationally inherited epigenetic expression states.
DNA 复制受损是癌症的一个标志,也是基因组不稳定的一个原因。我们报告说,除了导致遗传变化外,胚胎发育过程中 DNA 复制受损还会对基因组产生重大的表观遗传后果。在全基因组筛选中,我们发现 DNA 复制受损是导致. 中被抑制的转基因表达增加的原因。获得的表达状态表现为一个“表观等位基因”,在完全重置之前,它可以在多个世代中遗传。去抑制不仅限于转基因,而是由于早期胚胎中复制过程中修饰的组蛋白在 DNA 上的保留受损,导致异染色质相关组蛋白修饰的全局减少所致。因此,发育过程中 DNA 复制受损可全局去抑制染色质,产生新的可遗传的表观遗传表达状态。