Clerc R G, Bucher P, Strub K, Birnstiel M L
Nucleic Acids Res. 1983 Dec 20;11(24):8641-57. doi: 10.1093/nar/11.24.8641.
A cloned Xenopus laevis H4 histone gene has been expressed in the X.laevis oocyte nucleus. The homologous histone H4 gene can be correctly and efficiently expressed in the frog oocyte even in presence of bacterial vector DNA. As revealed by both analytical gel electrophoresis and S1 mapping, two H4 mRNAs are specified with different transcriptional efficiencies from the tandemly repeated promoter. Results from deletion mapping of the sequences essential for promoting H4 transcription show that drastic reduction of transcription is obtained when the sequences lying between -64 and -35 bp from the mRNA cap site are removed. We demonstrate by DNA sequence comparison using a novel computer program that this important area of the H4 promoter contains two highly conserved DNA motifs near positions -51 to -46 upstream from the cap site in all H4 gene promoters analysed.
一个克隆的非洲爪蟾H4组蛋白基因已在非洲爪蟾卵母细胞核中表达。即使存在细菌载体DNA,同源组蛋白H4基因也能在蛙卵母细胞中正确且高效地表达。分析凝胶电泳和S1作图结果表明,串联重复启动子以不同的转录效率产生了两种H4 mRNA。对促进H4转录所必需的序列进行缺失作图的结果显示,当从mRNA帽位点起-64至-35 bp之间的序列被去除时,转录会急剧减少。我们使用一种新颖的计算机程序通过DNA序列比较证明,在所有分析的H4基因启动子中,H4启动子的这一重要区域在帽位点上游-51至-46位置附近包含两个高度保守的DNA基序。