Sowden J, Edwards M, Morrison K, Butterworth P H, Edwards Y H
MRC Human Biochemical Genetics Unit, Galton Laboratory (UCL), London, U.K.
Biochem J. 1992 Dec 1;288 ( Pt 2)(Pt 2):545-51. doi: 10.1042/bj2880545.
The carbonic anhydrase 1 gene is expressed in adult human and mouse erythroid cells and colon epithelia from two distinct promoters. We have explored the erythroid promoter for cis-acting sequences involved in transcription using DNAaseI as a probe. Two DNAaseI-hypersensitive sites (DHS-1 and DHS-2) have been identified in the distal erythroid promoter in CA1-expressing erythroleukaemic cells. These sites are present at low levels in K562 cells, which have a foetal/embryonic phenotype and do not express CA1. DHS-1 and DHS-2 are not present in non-erythroid cells, including colon cells, which express CA1 from the proximal colon promoter. DHS-1 and DHS-2 were also generated in an heterologous CA1 gene containing 5 kb of erythroid promoter sequence after transfection into erythroid cells, including K562 cells. These transfection studies showed that both this fragment, and an abbreviated 817 bp promoter fragment which contains only DHS-1, were sufficient to confer erythroid-specific expression to a reporter gene. These promoters were active in cell lines expressing CA1 and in K562 cells. This latter observation implies that a developmental repressor factor is both present in K562 cells and binds to a cis-acting sequence that is absent from the sequence 5 kb upstream of the erythroid transcription start site.
碳酸酐酶1基因通过两个不同的启动子在成年人类和小鼠的红细胞及结肠上皮细胞中表达。我们使用DNA酶I作为探针,探索了参与转录的红细胞启动子中的顺式作用序列。在表达CA1的红白血病细胞的远端红细胞启动子中已鉴定出两个DNA酶I高敏位点(DHS-1和DHS-2)。这些位点在具有胎儿/胚胎表型且不表达CA1的K562细胞中含量较低。DHS-1和DHS-2在包括结肠细胞在内的非红细胞中不存在,结肠细胞从近端结肠启动子表达CA1。在转染到包括K562细胞在内的红细胞后,在含有5 kb红细胞启动子序列的异源CA1基因中也产生了DHS-1和DHS-2。这些转染研究表明,该片段以及仅包含DHS-1的817 bp缩写启动子片段都足以赋予报告基因红细胞特异性表达。这些启动子在表达CA1的细胞系和K562细胞中具有活性。后一观察结果表明,发育抑制因子既存在于K562细胞中,又与红细胞转录起始位点上游5 kb序列中不存在的顺式作用序列结合。