首页> 美国卫生研究院文献>Nucleic Acids Research >Activation and repression of Drosophila alcohol dehydrogenase distal transcription by two steroid hormone receptor superfamily members binding to a common response element.
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Activation and repression of Drosophila alcohol dehydrogenase distal transcription by two steroid hormone receptor superfamily members binding to a common response element.

机译:果蝇酒精脱氢酶远端转录的激活和抑制作用是通过两个类固醇激素受体超家族成员与一个共同的应答元件结合而实现的。

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摘要

Developmental activation of the Drosophila alcohol dehydrogenase (Adh) distal promoter is controlled by the Adh adult enhancer (AAE). Within this 150 bp, complex enhancer is a small (12 bp) positive cis-acting element that is required for high levels of distal transcription in adult flies and ADH-expressing tissue culture cells. We previously reported that the steroid receptor superfamily member FTZ-F1 binds to this site. We have identified a second steroid receptor superfamily member, DHR39, which also binds to this site. DHR39 is expressed throughout development in transcripts of several sizes. In situ hybridization to embryos has shown that DHR39 RNA is found primarily in the central nervous system, and not in embryonic tissues that express ADH. FTZ-F1 RNA, however, shows temporal-specific patterns similar to those of the distal promoter. FTZ-F1 and DHR39 have identical amino acids in the 'P-box' of the DNA binding domain, suggesting that they have identical DNA recognition characteristics. By electrophoretic mobility shift analysis we show that a DHR39 fusion protein binds specifically to two FTZ-F1 binding sites. By over expressing the full length DHR39 protein in a transient co-transfection assay we have shown that it represses distal Adh expression in a dosage- and binding site-dependent manner. Over expression of an alternative DHR39 open reading frame that lacks part of the putative ligand binding domain does not alter Adh expression. In contrast, over expression of FTZ-F1 specifically activates distal Adh expression.
机译:果蝇酒精脱氢酶(Adh)远端启动子的发育激活受Adh成人增强子(AAE)控制。在这个150 bp的范围内,复合增强子是小的(12 bp)正顺式作用元件,是成年果蝇和表达ADH的组织培养细胞中高水平远侧转录所必需的。我们先前曾报道类固醇受体超家族成员FTZ-F1结合到该位点。我们已经确定了第二个类固醇受体超家族成员DHR39,它也与该位点结合。在整个开发过程中,DHR39均以多种大小的转录本表达。与胚胎的原位杂交表明,DHR39 RNA主要存在于中枢神经系统中,而不存在于表达ADH的胚胎组织中。然而,FTZ-F1 RNA显示出与远端启动子相似的时间特异性模式。 FTZ-F1和DHR39在DNA结合域的“ P-box”中具有相同的氨基酸,这表明它们具有相同的DNA识别特性。通过电泳迁移率迁移分析,我们显示DHR39融合蛋白特异性结合两个FTZ-F1结合位点。通过在瞬时共转染测定中过表达全长DHR39蛋白,我们已显示出它以剂量和结合位点依赖性方式抑制远端Adh表达。缺少假定的配体结合结构域的一部分的替代DHR39开放阅读框的过度表达不会改变Adh表达。相反,FTZ-F1的过度表达会特异性激活远端Adh表达。

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