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The p68 and p72 DEAD box RNA helicases interact with HDAC1 and repress transcription in a promoter-specific manner

机译:p68和p72 DEAD盒RNA解旋酶与HDAC1相互作用并以启动子特异性方式抑制转录

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Background p68 (Ddx5) and p72 (Ddx17) are highly related members of the DEAD box family and are established RNA helicases. They have been implicated in growth regulation and have been shown to be involved in both pre-mRNA and pre-rRNA processing. More recently, however, these proteins have been reported to act as transcriptional co-activators for estrogen-receptor alpha (ERα). Furthermore these proteins were shown to interact with co-activators p300/CBP and the RNA polymerase II holoenzyme. Taken together these reports suggest a role for p68 and p72 in transcriptional activation. Results In this report we show that p68 and p72 can, in some contexts, act as transcriptional repressors. Targeting of p68 or p72 to constitutive promoters leads to repression of transcription; this repression is promoter-specific. Moreover both p68 and p72 associate with histone deacetylase 1 (HDAC1), a well-established transcriptional repression protein. Conclusions It is therefore clear that p68 and p72 are important transcriptional regulators, functioning as co-activators and/or co-repressors depending on the context of the promoter and the transcriptional complex in which they exist.
机译:背景p68(Ddx5)和p72(Ddx17)是DEAD盒家族的高度相关成员,是已建立的RNA解旋酶。它们已经牵涉到生长调节,并且已经显示出它们参与了前mRNA和前rRNA加工。然而,最近,据报道这些蛋白质充当雌激素受体α(ERα)的转录共激活因子。此外,这些蛋白还显示出与共激活因子p300 / CBP和RNA聚合酶II全酶相互作用。这些报告合起来提示p68和p72在转录激活中的作用。结果在本报告中,我们表明p68和p72在某些情况下可以充当转录阻遏物。将p68或p72靶向组成型启动子可导致转录抑制。这种抑制是启动子特异性的。此外,p68和p72均与组蛋白脱乙酰基酶1(HDAC1)相关,后者是一种公认​​的转录抑制蛋白。结论因此,很明显p68和p72是重要的转录调节因子,根据启动子和它们所存在的转录复合体的情况,它们起着共激活因子和/或共抑制因子的作用。

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