Department of Biological Science, Florida State University, 319 Stadium Drive, Tallahassee, FL 32306, USA.
Department of Biology, Emory University, Atlanta, GA 30322, USA.
Stem Cell Reports. 2019 Jul 9;13(1):193-206. doi: 10.1016/j.stemcr.2019.05.021. Epub 2019 Jun 20.
The temporal order of DNA replication is regulated during development and is highly correlated with gene expression, histone modifications and 3D genome architecture. We tracked changes in replication timing, gene expression, and chromatin conformation capture (Hi-C) A/B compartments over the first two cell cycles during differentiation of human embryonic stem cells to definitive endoderm. Remarkably, transcriptional programs were irreversibly reprogrammed within the first cell cycle and were largely but not universally coordinated with replication timing changes. Moreover, changes in A/B compartment and several histone modifications that normally correlate strongly with replication timing showed weak correlation during the early cell cycles of differentiation but showed increased alignment in later differentiation stages and in terminally differentiated cell lines. Thus, epigenetic cell fate transitions during early differentiation can occur despite dynamic and discordant changes in otherwise highly correlated genomic properties.
DNA 复制的时间顺序在发育过程中受到调控,并且与基因表达、组蛋白修饰和 3D 基因组结构高度相关。我们在人类胚胎干细胞向原肠胚分化的前两个细胞周期中,追踪了复制时间、基因表达和染色质构象捕获(Hi-C)A/B 区室的变化。值得注意的是,转录程序在第一个细胞周期内不可逆地重新编程,并且与复制时间的变化在很大程度上但不是普遍协调。此外,A/B 区室和几种通常与复制时间密切相关的组蛋白修饰在分化的早期细胞周期中显示出较弱的相关性,但在后期分化阶段和终末分化的细胞系中显示出更强的一致性。因此,尽管在其他方面高度相关的基因组特性中存在动态和不和谐的变化,但早期分化过程中的表观遗传细胞命运转变仍可发生。