Institut Curie, 26 Rue d'Ulm, 75248 Paris Cedex 05, France; CNRS UMR3215, 75248 Paris Cedex 05, France; INSERM U934, 75248 Paris Cedex 05, France.
Institut Curie, 26 Rue d'Ulm, 75248 Paris Cedex 05, France.
Cell. 2014 May 8;157(4):950-63. doi: 10.1016/j.cell.2014.03.025.
A new level of chromosome organization, topologically associating domains (TADs), was recently uncovered by chromosome conformation capture (3C) techniques. To explore TAD structure and function, we developed a polymer model that can extract the full repertoire of chromatin conformations within TADs from population-based 3C data. This model predicts actual physical distances and to what extent chromosomal contacts vary between cells. It also identifies interactions within single TADs that stabilize boundaries between TADs and allows us to identify and genetically validate key structural elements within TADs. Combining the model's predictions with high-resolution DNA FISH and quantitative RNA FISH for TADs within the X-inactivation center (Xic), we dissect the relationship between transcription and spatial proximity to cis-regulatory elements. We demonstrate that contacts between potential regulatory elements occur in the context of fluctuating structures rather than stable loops and propose that such fluctuations may contribute to asymmetric expression in the Xic during X inactivation.
最近,通过染色体构象捕获(3C)技术发现了一种新的染色体组织层次,拓扑关联结构域(TAD)。为了探索 TAD 的结构和功能,我们开发了一种聚合物模型,可以从基于群体的 3C 数据中提取 TAD 内的全套染色质构象。该模型预测了实际的物理距离以及细胞间染色体接触的程度。它还识别了单个 TAD 内的相互作用,这些相互作用稳定了 TAD 之间的边界,并使我们能够识别和遗传验证 TAD 内的关键结构元素。将模型的预测与 X 染色体失活中心(Xic)内 TAD 的高分辨率 DNA FISH 和定量 RNA FISH 相结合,我们剖析了转录和与顺式调控元件空间接近之间的关系。我们证明,潜在调控元件之间的接触是在波动结构的背景下发生的,而不是稳定的环,并且提出这种波动可能有助于 X 染色体失活期间 Xic 中的不对称表达。