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Evolutionary comparison reveals that diverging CTCF sites are signatures of ancestral topological associating domains borders

机译:进化比较表明,不同的CTCF位点是祖先拓扑关联域边界的特征

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摘要

Increasing evidence in the last years indicates that the vast amount of regulatory information contained in mammalian genomes is organized in precise 3D chromatin structures. However, the impact of this spatial chromatin organization on gene expression and its degree of evolutionary conservation is still poorly understood. The Six homeobox genes are essential developmental regulators organized in gene clusters conserved during evolution. Here, we reveal that the Six clusters share a deeply evolutionarily conserved 3D chromatin organization that predates the Cambrian explosion. This chromatin architecture generates two largely independent regulatory landscapes (RLs) contained in two adjacent topological associating domains (TADs). By disrupting the conserved TAD border in one of the zebrafish Six clusters, we demonstrate that this border is critical for preventing competition between promoters and enhancers located in separated RLs, thereby generating different expression patterns in genes located in close genomic proximity. Moreover, evolutionary comparison of Six-associated TAD borders reveals the presence of CCCTC-binding factor (CTCF) sites with diverging orientations in all studied deuterostomes. Genome-wide examination of mammalian HiC data reveals that this conserved CTCF configuration is a general signature of TAD borders, underscoring that common organizational principles underlie TAD compartmentalization in deuterostome evolution.
机译:近年来,越来越多的证据表明,哺乳动物基因组中包含的大量监管信息是以精确的3D染色质结构组织的。然而,这种空间染色质组织对基因表达及其进化保守程度的影响仍然知之甚少。六个同源异型盒基因是必需的发育调节因子,组织成进化过程中保守的基因簇。在这里,我们揭示了六个簇在寒武纪爆炸之前共享了一个在进化上极为保守的3D染色质组织。这种染色质体系结构生成两个相邻的拓扑关联域(TAD)中包含的两个在很大程度上独立的调节域(RL)。通过破坏斑马鱼六个集群之一中的保守的TAD边界,我们证明了该边界对于防止位于分离的RLs中的启动子和增强子之间的竞争至关重要,从而在紧密基因组邻近的基因中产生不同的表达模式。此外,与六个相关的TAD边界的进化比较显示,在所有研究的子宫口中,CCCTC结合因子(CTCF)位点的方向不同。哺乳动物HiC数据的全基因组检查显示,这种保守的CTCF配置是TAD边界的一般特征,强调了共同的组织原理是氘化造口组进化过程中TAD分隔的基础。

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