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Jpx RNA activates xist by evicting CTCF

机译:Jpx RNA通过驱逐CTCF激活xist

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Summary In mammals, dosage compensation between XX and XY individuals occurs through X chromosome inactivation (XCI). The noncoding Xist RNA is expressed and initiates XCI only when more than one X chromosome is present. Current models invoke a dependency on the X-to-autosome ratio (X:A), but molecular factors remain poorly defined. Here, we demonstrate that molecular titration between an X-encoded RNA and an autosomally encoded protein dictates Xist induction. In pre-XCI cells, CTCF protein represses Xist transcription. At the onset of XCI, Jpx RNA is upregulated, binds CTCF, and extricates CTCF from one Xist allele. We demonstrate that CTCF is an RNA-binding protein and is titrated away from the Xist promoter by Jpx RNA. Thus, Jpx activates Xist by evicting CTCF. The functional antagonism via molecular titration reveals a role for long noncoding RNA in epigenetic regulation. PaperFlick
机译:小结在哺乳动物中,XX和XY个体之间的剂量补偿是通过X染色体失活(XCI)进行的。仅当存在多个X染色体时,才会表达非编码Xist RNA并启动XCI。当前的模型引起对X染色体常染色体比率(X:A)的依赖性,但是分子因素仍然定义不清。在这里,我们证明X编码的RNA和常染色体编码的蛋白质之间的分子滴定决定了Xist的诱导。在XCI前细胞中,CTCF蛋白抑制Xist转录。在XCI发生时,Jpx RNA被上调,结合CTCF,并从一个Xist等位基因中解脱CTCF。我们证明CTCF是一种RNA结合蛋白,并通过Jpx RNA从Xist启动子滴定。因此,Jpx通过驱逐CTCF来激活Xist。通过分子滴定的功能拮抗作用揭示了长非编码RNA在表观遗传调控中的作用。 PaperFlick

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