Mader S, Thiele K, Breuer B, Alonso A
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Strasbourg, France.
J Mol Biol. 1994 Sep 9;242(1):37-44. doi: 10.1006/jmbi.1994.1555.
Retinoic-acid mediated differentiation of F9 cells is accompanied by an increased transcription of the histone H1zero gene. This increase is an early response after addition of retinoic acid, suggesting a direct effect of the hormone on transcription of the gene. We show now that the promoter of histone H1zero contains a DNA element, localized 531 base-pairs upstream of the cap site, that is composed of a direct repeat of the sequence PuGGTCA separated by eight base-pairs. This element confers retinoic acid responsiveness to a heterologous thymidine kinase promoter in F9 and HeLa cells. Furthermore, the element forms retarded complexes not only with bacterially expressed retinoic acid receptors (RARs) and retinoid X receptors (RXRs), but also with endogenous F9 receptors. Our results suggest therefore that retinoic acid receptors can control the expression of a chromatin structural gene the expression of which is associated with a differentiated phenotype.
维甲酸介导的F9细胞分化伴随着组蛋白H1零基因转录的增加。这种增加是添加维甲酸后的早期反应,表明该激素对基因转录有直接作用。我们现在表明,组蛋白H1零的启动子包含一个DNA元件,位于帽位点上游531个碱基对处,由序列PuGGTCA的直接重复组成,中间间隔8个碱基对。该元件赋予F9和HeLa细胞中的异源胸苷激酶启动子维甲酸反应性。此外,该元件不仅与细菌表达的维甲酸受体(RAR)和类视黄醇X受体(RXR)形成阻滞复合物,还与内源性F9受体形成阻滞复合物。因此,我们的结果表明,维甲酸受体可以控制一种染色质结构基因的表达,该基因的表达与分化表型相关。