Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Cell. 2013 Jan 31;152(3):642-54. doi: 10.1016/j.cell.2012.12.033. Epub 2013 Jan 17.
Differences in chromatin organization are key to the multiplicity of cell states that arise from a single genetic background, yet the landscapes of in vivo tissues remain largely uncharted. Here, we mapped chromatin genome-wide in a large and diverse collection of human tissues and stem cells. The maps yield unprecedented annotations of functional genomic elements and their regulation across developmental stages, lineages, and cellular environments. They also reveal global features of the epigenome, related to nuclear architecture, that also vary across cellular phenotypes. Specifically, developmental specification is accompanied by progressive chromatin restriction as the default state transitions from dynamic remodeling to generalized compaction. Exposure to serum in vitro triggers a distinct transition that involves de novo establishment of domains with features of constitutive heterochromatin. We describe how these global chromatin state transitions relate to chromosome and nuclear architecture, and discuss their implications for lineage fidelity, cellular senescence, and reprogramming.
染色质构象的差异是细胞在单一遗传背景下产生多种状态的关键,但体内组织的图谱在很大程度上仍未被描绘。在这里,我们对大量多样化的人类组织和干细胞进行了全基因组范围的染色质作图。这些图谱提供了前所未有的功能基因组元件及其在发育阶段、谱系和细胞环境中的调控的注释。它们还揭示了与核架构相关的表观基因组的全局特征,这些特征也随细胞表型的变化而变化。具体而言,随着默认状态从动态重塑转变为普遍紧缩,发育特化伴随着染色质的逐渐限制。体外接触血清会引发一个独特的转变,涉及到具有组成型异染色质特征的新域的建立。我们描述了这些全局染色质状态转变如何与染色体和核架构相关,并讨论了它们对谱系保真度、细胞衰老和重编程的影响。