Sturm R A, Dalton S, Wells J R
Department of Biochemistry, University of Adelaide, South Australia.
Nucleic Acids Res. 1988 Sep 12;16(17):8571-86. doi: 10.1093/nar/16.17.8571.
The organization and function of potential regulatory elements associated with the promoters of chicken H2A and H2B genes pairs have been examined. The intergene regions of six dispersed and divergently-transcribed H2A/H2B gene pairs contain several extremely well conserved and spaced blocks of sequence homology. Adjacent coding regions are on average 342 base-pairs apart. Respective TATA boxes are separated by 180 base-pairs and within this confined region there are four CCAAT boxes and a previously identified 13 base-pair H2B-specific element (H2B-box) which has homology to the octamer motif present in a number of gene promoter/enhancer elements. Transcription of H2A and H2B genes from wild-type and mutant constructs was measured in transient assays by transfection into HeLa cells, and in permanently transformed clonal cell lines. In vitro separation of the two genes at a unique intergenic site significantly decreased transcription of each gene. This suggested that the H2A/H2B gene pairs contained overlapping promoters. Deletion or point mutagenesis of the H2B-specific element decreased the levels of H2B and the H2A transcripts indicating that this sequence is a common regulatory element of both genes in the divergent-pair configeration.
对鸡H2A和H2B基因对启动子相关潜在调控元件的组织和功能进行了研究。六个分散且转录方向相反的H2A/H2B基因对的基因间区域包含几个高度保守且间隔良好的序列同源性区域。相邻的编码区域平均相距342个碱基对。各自的TATA盒相隔180个碱基对,在这个有限区域内有四个CCAAT盒和一个先前鉴定的13个碱基对的H2B特异性元件(H2B盒),它与许多基因启动子/增强子元件中存在的八聚体基序具有同源性。通过转染到HeLa细胞的瞬时分析以及在永久转化的克隆细胞系中,测量了野生型和突变构建体中H2A和H2B基因的转录。在一个独特的基因间位点对这两个基因进行体外分离显著降低了每个基因的转录。这表明H2A/H2B基因对包含重叠的启动子。H2B特异性元件的缺失或点突变降低了H2B和H2A转录本的水平,表明该序列是不同对构型中两个基因的共同调控元件。