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A novel E2 box-GATA element modulates Cdc6 transcription during human cells polyploidization

机译:一种新型的E2 box-GATA元件在人类细胞多倍化过程中调控Cdc6转录

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摘要

Cdc6 is a key regulator of the strict alternation of S and M phases during the mitotic cell cycle. In mammalian and plant cells that physiologically become polyploid, cdc6 is transcriptionally and post-translationally regulated. We have recently reported that Cdc6 levels are maintained in megakaryoblastic HEL cells, but severely downregulated by ectopic expression of transcriptional repressor Drosophila melanogaster escargot. Here, we show that cdc6 promoter activity is upregulated during megakaryocytic differentiation of HEL endoreplicating cells, and that Escargot interferes with such activation. Transactivation experiments showed that a 1.7 kb region located at 2800 upstream cdc6 transcription initiation site behaved as a potent enhancer in endoreplicating cells only. This activity was mainly dependent on a novel cis-regulatory element composed by an E2 box overlapping a GATA motif. Ectopic Escargot could bind this regulatory element in vitro and endogenous GATA-1 and E2A formed specific complexes in megakaryoblastic cells as well as in primary megakaryocytes. Chromatin Immunoprecipitation analysis revealed that both transcription factors were occupying the E2 box/GATA site in vivo. Altogether, these data suggest that cdc6 expression could be actively maintained during megakaryocytic differentiation through transcriptional mechanisms involving specific cis- and trans-regulatory elements.
机译:Cdc6是有丝分裂细胞周期中S和M期严格交替的关键调节因子。在生理上变成多倍体的哺乳动物和植物细胞中,cdc6受转录和翻译后调控。我们最近报道,巨核母细胞HEL细胞中Cdc6水平得以维持,但转录阻遏物果蝇Escargot的异位表达严重下调了Cdc6水平。在这里,我们表明在HEL内复制细胞的巨核细胞分化过程中,cdc6启动子活性被上调,而Escargot干扰了这种激活。反式激活实验表明,位于2800个上游cdc6转录起始位点的1.7 kb区域仅在复制内膜的细胞中充当强效增强剂。该活性主要取决于由与GATA基序重叠的E2盒组成的新型顺式调控元件。异位田螺可以在体外结合该调节元件,内源性GATA-1和E2A在巨核细胞和原代巨核细胞中形成特异性复合物。染色质免疫沉淀分析表明,两种转录因子均在体内占据着E2 box / GATA位点。总之,这些数据表明,通过涉及特定顺式和反式调控元件的转录机制,在巨核细胞分化过程中可以积极维持cdc6的表达。

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