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Transcriptional potential of the γ-globin gene is dependent on the CACCC box in a developmental stage-specific manner

机译:γ-珠蛋白基因的转录潜力以发育阶段特异性方式依赖于CACCC盒

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摘要

To test the role of CACCC box on γ-globin gene activation, the CACCC box was deleted or mutated and γ-gene expression was monitored in transgenic mice. Disruption of the CACCC box had no effect on γ-gene expression in the cells of embryonic erythropoiesis but it strikingly reduced γ-gene expression in fetal erythropoiesis, and abolished γ-gene expression in adult erythroid cells. The CACCC mutation diminished HS formation, as well as TBP and polII recruitment at the γ-gene promoter; however, it only resulted in slight or no effects on histone H3 and H4 acetylation in adult erythropoiesis. Our findings indicate that each basic cis element of the proximal γ-gene promoter, i.e. CACCC, CCAAT or TATA box, can be disrupted without affecting the activation of γ gene in embryonic erythroid cells. We propose that the trans factors recruited by the three boxes interact with each other to form a ‘promoter complex’. In embryonic erythropoiesis the locus control region enhancer is able to interact with the complex even when components normally binding to one of the motifs are missing, but it can only activate an intact ‘promoter complex’ in adult erythroid cells.
机译:为了测试CACCC盒在γ-珠蛋白基因激活中的作用,删除或突变了CACCC盒,并在转基因小鼠中监测γ基因的表达。 CACCC盒的破坏对胚胎红细胞生成细胞中的γ基因表达没有影响,但显着降低了胎儿红细胞生成中的γ基因表达,并消除了成年红细胞中的γ基因表达。 CACCC突变减少了HS基因的形成以及γ基因启动子上的TBP和polII募集。然而,它仅对成年红细胞生成中的组蛋白H3和H4乙酰化作用影响很小或没有影响。我们的发现表明,可以破坏近端γ基因启动子的每个基本顺式元件,即CACCC,CCAAT或TATA盒,而不会影响胚胎红系细胞中γ基因的激活。我们建议,由三个盒子招募的反式因子彼此相互作用,形成一个“启动子复合体”。在胚胎红细胞生成过程中,基因座控制区增强子即使与正常基序之一结合的成分缺失也能与复合物相互作用,但它只能激活成年红细胞中完整的“启动子复合物”。

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