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Nsd2 Represses Endogenous Retrovirus MERVL in Embryonic Stem Cells

机译:NSD2在胚胎干细胞中抑制内源性逆转录病毒Merv1

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The facilitates chromatin transcription (FACT) complex is a histone H2A/H2B chaperone, which represses endogenous retroviruses (ERVs) and transcription of ERV-chimeric transcripts. It binds to both transcription start site and gene body region. Here, we investigated the downstream targets of FACT complex to identify the potential regulators of MERVL, which is a key 2-cell marker gene. H3K36me2 profile was positively correlated with that of FACT component Ssrp1. Among H3K36me2 deposition enzymes, Nsd2 was downregulated after the loss of Ssrp1 . Furthermore, we demonstrated that Nsd2 repressed the expression of ERVs without affecting the expression of pluripotency genes. The expression of MERVL and 2-cell genes was partially rescued by Nsd2 overexpression. The enrichment of H3K36me2 decreased on MERVL-chimeric gene in ESCs without Ssrp1 . Our study discovers that Nsd2 is a repressor of MERVL, and FACT partially represses MERVL expression by regulating the expression of Nsd2 and its downstream H3K36me2.
机译:促进染色质转录(事实)复合物是一种组蛋白H2A / H2B伴侣,其抑制内源性逆转录病毒(ERV)和ERV-嵌合转录物的转录。它与转录开始点和基因体区域结合。在这里,我们研究了事实复合物的下游靶标以鉴定Mervl的潜在调节剂,这是一个关键的2细胞标记基因。 H3K36ME2配置文件与事实组分SSRP1的配置文件呈正相关。在H3K36ME2沉积酶中,在损失SSRP1后下调NSD2。此外,我们证明NSD2在不影响多能基因表达的情况下抑制了ERV的表达。通过NSD2过表达部分地抵押Merv1和2细胞基因的表达。 H3K36ME2的富集在ESCS的Mervl-嵌合基因上减少而没有SSRP1。我们的研究发现NSD2是MervL的阻遏物,并且通过调节NSD2的表达及其下游H3K36Me2,事实是部分地抑制了MERVL表达。

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