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Np95 Is Implicated in Pericentromeric Heterochromatin Replication and in Major Satellite Silencing

机译:Np95牵涉到perenenttromeric异染色质复制和主要卫星沉默。

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摘要

Heterochromatin plays an important role in transcriptional repression, for the correct segregation of chromosomes and in the maintenance of genome stability. Pericentric heterochromatin (PH) replication and formation have been proposed to occur in the pericentric heterochromatin duplication body (pHDB). A central question is how the underacetylated state of heterochromatic histone H4 tail is established and controlled, because it is a key event during PH replication and is essential to maintain the compacted and silenced state of these regions. Np95 is a cell cycle regulated and is a nuclear histone-binding protein that also recruits HDAC-1 to target promoters. It is essential for S phase and for embryonic formation and is implicated in chromosome stability. Here we show that Np95 is part of the pHDB, and its functional ablation causes a strong reduction in PH replication. Depletion of Np95 also causes a hyperacetylation of lysines 8, 12, and 16 of heterochromatin histone H4 and an increase of pericentromeric major satellite transcription, whose RNAs are key players for heterochromatin formation. We propose that Np95 is a new relevant protein involved in heterochromatin replication and formation.
机译:异染色质在转录抑制,染色体的正确分离和基因组稳定性的维持中起着重要作用。已提出在外周中心异染色质复制体(pHDB)中发生外周中心异染色质(PH)复制和形成。一个中心问题是如何建立和控制异色组蛋白H4尾巴的欠乙酰化状态,因为这是PH复制过程中的关键事件,对于维持这些区域的压缩和沉默状态至关重要。 Np95是细胞周期调节的,是一种核组蛋白结合蛋白,也可以募集HDAC-1来靶向启动子。它对于S期和胚胎形成必不可少,并且与染色体稳定性有关。在这里,我们显示Np95是pHDB的一部分,其功能消融会导致PH复制强烈降低。 Np95的消耗也会引起异染色质组蛋白H4的赖氨酸8、12和16的过度乙酰化,以及着丝粒主要卫星转录的增加,后者的RNA是异染色质形成的关键因素。我们建议Np95是涉及异染色质复制和形成的一种新的相关蛋白。

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