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DNA BENDING BY THE SILENCER PROTEIN NEP1 IS MODULATED BY TR AND RXR

机译:沉默蛋白NEP1产生的DNA弯曲由TR和RXR调控

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摘要

NeP1 binds to the F1 silencer element of the chicken lysozyme gene and, in the presence of TR, v-ERBA or RAR, synergistically represses transcriptional activity. This repression involves a silencing mechanism acting independently of the relative promoter position, Here we show that NeP1 alone can induce a significant directed bend on DNA. The chicken homologue of human NeP1, CTCF, shows identical binding and bending properties, in contrast, the isolated DNA binding domain of CTCF efficiently binds DNA, but fails to confer bending, Similarly, the TR-RXR hetero- or homodimer, binding adjacent to NeP1 at the F2 sequence, do not show significant DNA bending, The binding of the T3 ligand to TR changes neither the magnitude nor the direction of the NeP1 induced bend, However, when all factors are bound simultaneously as a quaternary complex, the TR-RXR heterodimer changes the location of the bend center, the flexure angle and the bending direction.
机译:NeP1结合鸡溶菌酶基因的F1沉默子元件,并在存在TR,v-ERBA或RAR的情况下协同抑制转录活性。这种压制涉及独立于相对启动子位置起作用的沉默机制。在这里,我们表明,单独的NeP1可以诱导DNA上明显的定向弯曲。人NeP1 CTCF的鸡同源物显示出相同的结合和弯曲特性,相比之下,CTCF的分离的DNA结合结构域可以有效地结合DNA,但不能赋予弯曲作用。类似地,TR-RXR异源或同源二聚体与F2序列上的NeP1没有明显的DNA弯曲,T3配体与TR的结合既不会改变NeP1诱导的弯曲的大小,也不会改变其方向,但是,当所有因子同时以四元络合物的形式结合时,TR- RXR异二聚体可改变弯曲中心的位置,弯曲角度和弯曲方向。

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