School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Department of Genetics and Evolution, University of Geneva, Geneva, Switzerland.
Elife. 2020 Apr 17;9:e52962. doi: 10.7554/eLife.52962.
Developmental genes are often controlled by large regulatory landscapes matching topologically associating domains (TADs). In various contexts, the associated chromatin backbone is modified by specific enhancer-enhancer and enhancer-promoter interactions. We used a TAD flanking the mouse cluster to study how these regulatory architectures are formed and deconstructed once their function achieved. We describe this TAD as a functional unit, with several regulatory sequences acting together to elicit a transcriptional response. With one exception, deletion of these sequences didn't modify the transcriptional outcome, a result at odds with a conventional view of enhancer function. The deletion and inversion of a CTCF site located near these regulatory sequences did not affect transcription of the target gene. Slight modifications were nevertheless observed, in agreement with the loop extrusion model. We discuss these unexpected results considering both conventional and alternative explanations relying on the accumulation of poorly specific factors within the TAD backbone.
发育基因通常受与拓扑关联域 (TAD) 相匹配的大型调控景观控制。在各种情况下,相关染色质骨架通过特定的增强子-增强子和增强子-启动子相互作用进行修饰。我们使用侧翼的小鼠簇来研究这些调控结构是如何形成的,以及一旦它们的功能实现,又是如何被解构的。我们将这个 TAD 描述为一个功能单元,其中几个调控序列共同作用以引发转录反应。除了一个例外,这些序列的缺失并没有改变转录结果,这与增强子功能的传统观点不一致。位于这些调控序列附近的 CTCF 位点的缺失和倒位并没有影响靶基因的转录。然而,观察到了轻微的修饰,这与环挤出模型一致。我们考虑了传统和替代的解释,这些解释都依赖于 TAD 骨架内积累的非特异性较差的因子,从而讨论了这些出乎意料的结果。