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Gene-specific factors determine mitotic expression and bookmarking via alternate regulatory elements

机译:基因特异性因子通过其他调控元件决定有丝分裂表达和书签

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摘要

Transcriptional silencing during mitosis is caused by inactivation of critical transcriptional regulators and/or chromatin condensation. Inheritance of gene expression patterns through cell division involves various bookmarking mechanisms. In this report, we have examined the mitotic and post-mitotic expression of the DRA major histocompatibility class II (MHCII) gene in different cell types. During mitosis the constitutively MHCII-expressing B lymphoblastoid cells showed sustained occupancy of the proximal promoter by the cognate enhanceosome and general transcription factors. In contrast, although mitotic epithelial cells were depleted of these proteins irrespectively of their MHCII transcriptional activity, a distal enhancer selectively recruited the PP2A phosphatase via NFY and maintained chromatin accessibility. Based on our data, we propose a novel chromatin anti-condensation role for this element in mitotic bookmarking and timing of post-mitotic transcriptional reactivation.
机译:有丝分裂过程中的转录沉默是由关键转录调节因子的失活和/或染色质浓缩引起的。通过细胞分裂的基因表达模式的遗传涉及各种书签机制。在此报告中,我们检查了DRA主要组织相容性II类(MHCII)基因在不同细胞类型中的有丝分裂和有丝分裂后表达。在有丝分裂期间,组成型表达MHCII的B淋巴母细胞显示了同源增强体和一般转录因子对近端启动子的持续占据。相比之下,尽管有丝分裂上皮细胞的这些蛋白质都被耗尽,无论其MHCII转录活性如何,但远端增强子均通过NFY选择性地募集了PP2A磷酸酶,并保持了染色质的可及性。根据我们的数据,我们提出了一种新的染色质抗凝作用,此元素在有丝分裂书签和有丝分裂后转录重新激活的时机中具有一定的作用。

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