Gutman A, Gilthorpe J, Rigby P W
Laboratory of Eukaryotic Molecular Genetics, MRC National Institute for Medical Research, London, England.
Mol Cell Biol. 1994 Dec;14(12):8143-54. doi: 10.1128/mcb.14.12.8143-8154.1994.
Mouse Hoxb-4 (Hox-2.6) is a homeobox gene that belongs to a family which also includes Hoxa-4, Hoxc-4, and Hoxd-4 and that is related to the Deformed gene in Drosophila melanogaster. We have determined the sequence of 1.2 kb of 5' flanking DNA of mouse Hoxb-4 and by nuclease S1 and primer extension experiments identified two transcription start sites, P1 and P2, 285 and 207 nucleotides upstream of the ATG initiator codon, respectively. We have shown that this region harbors two independent promoters which drive CAT expression in several different cell lines with various efficiencies, suggesting that they are subject to cell-type-specific regulation. Through detailed mutational analysis, we have identified several cis-regulatory elements, located upstream and downstream of the transcription start sites. They include two cell-type-specific negative regulatory elements, which are more active in F9 embryonal carcinoma cells than in neuroblastoma cells (regions a and d at -226 to -186 and +169 to +205, respectively). An additional negative regulatory element has been delimited (region b between +22 and +113). Positive regulation is achieved by binding of HoxTF, a previously unknown factor, to the sequence GCCATTGG (+148 to +155) that is essential for efficient Hoxb-4 expression. We have also defined the minimal promoter sequences and found that they include two 12-bp initiator elements centered around each transcription start site. The complex architecture of the Hoxb-4 promoter provides the framework for fine-tuned transcriptional regulation during embryonic development.
小鼠Hoxb-4(Hox-2.6)是一种同源异型框基因,属于一个家族,该家族还包括Hoxa-4、Hoxc-4和Hoxd-4,并且与黑腹果蝇中的畸形基因相关。我们已经确定了小鼠Hoxb-4的1.2 kb 5'侧翼DNA序列,并通过核酸酶S1和引物延伸实验确定了两个转录起始位点P1和P2,分别位于ATG起始密码子上游285和207个核苷酸处。我们已经表明,该区域含有两个独立的启动子,它们以不同的效率驱动几种不同细胞系中的CAT表达,这表明它们受到细胞类型特异性调控。通过详细的突变分析,我们确定了位于转录起始位点上游和下游的几个顺式调控元件。它们包括两个细胞类型特异性负调控元件,在F9胚胎癌细胞中比在神经母细胞瘤细胞中更活跃(分别位于-226至-186和+169至+205的区域a和d)。另一个负调控元件已被划定(位于+22至+113之间的区域b)。通过一种先前未知的因子HoxTF与序列GCCATTGG(+148至+155)结合来实现正调控,该序列对于高效的Hoxb-4表达至关重要。我们还确定了最小启动子序列,发现它们包括围绕每个转录起始位点的两个12 bp起始元件。Hoxb-4启动子的复杂结构为胚胎发育过程中的微调转录调控提供了框架。