Edelmann L, Childs G
Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Gene Expr. 1998;7(3):133-47.
The sea urchin late histone H1 genes are expressed at low levels up until mid-blastula stage of development when an enhancer element activates transcription to higher levels. Stage-specific activator protein (SSAP) was previously identified as the transcription factor that binds to a sequence motif within the late H1-specific enhancer, USE IV, and mediates this stage-specific activation. However, another conserved late H1-specific element, USE III, was also shown to contribute to the activated expression of the late H1 genes. To attain a better understanding of the mechanism of blastula stage activation an extended analysis of the late H1-specific DNA sequences of the SpH1beta gene was performed. Our findings indicate that this region, located between positions -320 and -200, consists of three SSAP binding sites, USE IV, USE III, and another site located between the two, termed Site 2. Although SSAP binds to USE IV in vitro with 10-15-fold higher affinity than to either of the other two sites, multiple sites are necessary for activation. Multimers of either USE IV or USE III activate mid-blastula stage transcription to similar levels in the context of a functional H1beta basal promoter, but not with a TATA box alone. In addition, multimers of USE IV activate expression of a reporter construct containing an early histone H1 promoter at an embryonic stage when it is normally repressed. We propose a mechanism for mid-blastula activation of the late histone H1 genes where SSAP binding sites activate expression, but require the presence of the cis sequences of the basal promoter to function.
海胆晚期组蛋白H1基因在发育至囊胚中期之前表达水平较低,此时一个增强子元件将转录激活至更高水平。阶段特异性激活蛋白(SSAP)先前被鉴定为与晚期H1特异性增强子USE IV内的序列基序结合并介导这种阶段特异性激活的转录因子。然而,另一个保守的晚期H1特异性元件USE III也被证明有助于晚期H1基因的激活表达。为了更好地理解囊胚期激活机制,对SpH1β基因的晚期H1特异性DNA序列进行了扩展分析。我们的研究结果表明,该区域位于-320至-200位之间,由三个SSAP结合位点组成,即USE IV、USE III以及位于两者之间的另一个位点,称为位点2。尽管SSAP在体外与USE IV的结合亲和力比与其他两个位点中的任何一个高10 - 15倍,但激活需要多个位点。在功能性H1β基础启动子的背景下,USE IV或USE III的多聚体均可将囊胚中期转录激活至相似水平,但单独使用TATA盒则不行。此外,在胚胎期通常被抑制时,USE IV的多聚体可激活含有早期组蛋白H1启动子的报告基因构建体的表达。我们提出了一种晚期组蛋白H1基因囊胚中期激活的机制,其中SSAP结合位点激活表达,但需要基础启动子的顺式序列存在才能发挥作用。