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HoxB domain induction silences DNA replication origins in the locus and specifies a single origin at its boundary

机译:HoxB结构域诱导沉默基因座中的DNA复制起点并在其边界处指定一个起点

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摘要

In multicellular organisms, changes in the DNA replication programme could act to integrate differentiation with cell division in various developmental and transcriptional contexts. Here, we have addressed the use of DNA replication origins during differentiation in the HoxB domain—a cluster of nine genes developmentally regulated in a collinear manner. In undifferentiated mouse P19 cells, we detected several DNA replication origins in the 100 kb HoxB locus, indicating a relaxed origin use when the locus is transcriptionally silent. By contrast, in retinoic-acid-induced differentiated cells, when HoxB transcription is activated, a general silencing of DNA replication origins occurs in the locus except one located downstream of Hoxb1, at the 3′ boundary of the HoxB domain. Silencing of the replication origins is associated with histone hyperacetylation, whereas the active Hoxb1 origin persists as a hypoacetylated island. These findings provide direct evidence for the differentiated use of origins in HoxB genes, and we suggest that this regulation might contribute to the regulated expression of HoxB genes during development.
机译:在多细胞生物中,DNA复制程序的改变可能会在各种发育和转录环境中起到整合分化与细胞分裂的作用。在这里,我们已经解决了HoxB域分化过程中DNA复制起点的使用-HoxB域是共线方式发育调控的9个基因的簇。在未分化的小鼠P19细胞中,我们在100 kb HoxB基因座中检测到多个DNA复制起点,表明该基因座在转录沉默时使用了宽松的起点。相反,在视黄酸诱导的分化细胞中,当激活HoxB转录时,DNA复制起点的一般沉默发生在除了Hoxb1域下游3'边界处Hoxb1下游的一个基因座之外。复制起点的沉默与组蛋白超乙酰化有关,而活性Hoxb1起点则作为低乙酰化岛而持续存在。这些发现为HoxB基因起源的不同用途提供了直接的证据,我们建议这种调控可能有助于发育过程中HoxB基因的调控表达。

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