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Clustering of strong replicators associated with active promoters is sufficient to establish an early‐replicating domain

机译:与活性启动子相关的强复制剂的聚类足以建立早期复制域

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摘要

Vertebrate genomes replicate according to a precise temporal program strongly correlated with their organization into A/B compartments. Until now, the molecular mechanisms underlying the establishment of early‐replicating domains remain largely unknown. We defined two minimal cis‐element modules containing a strong replication origin and chromatin modifier binding sites capable of shifting a targeted mid‐late‐replicating region for earlier replication. The two origins overlap with a constitutive or a silent tissue‐specific promoter. When inserted side‐by‐side, these modules advance replication timing over a 250 kb region through the cooperation with one endogenous origin located 30 kb away. Moreover, when inserted at two chromosomal sites separated by 30 kb, these two modules come into close physical proximity and form an early‐replicating domain establishing more contacts with active A compartments. The synergy depends on the presence of the active promoter/origin. Our results show that clustering of strong origins located at active promoters can establish early‐replicating domains.
机译:脊椎动物基因组根据与其组织强烈相关的精确时间程序复制到A / B隔间。到目前为止,底层建立早期复制域的分子机制仍然很大程度上是未知的。我们定义了两个最小的顺式元素模块,其包含能够改变初期复制的靶向中期复制区域的强复制源和染色质修饰件结合位点。这两项起源与组成型或静音组织特异性启动子重叠。当并排插入时,这些模块通过与位于30kb的内源原点的合作,通过250 kB区域提高复制时序。此外,当插入30kb分离的两个染色体位点时,这两个模块接近物理接近,并形成了一种早期复制域,该域与有源隔室建立更多的接触。协同作用取决于有源启动子/起源的存在。我们的研究结果表明,位于活性启动子的强源性群体可以建立早期复制域。

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