Sharpe J A, Summerhill R J, Vyas P, Gourdon G, Higgs D R, Wood W G
MRC Molecular Haematology Unit, University of Oxford, John Radcliffe Hospital, UK.
Blood. 1993 Sep 1;82(5):1666-71.
Erythroid-specific DNase 1 hypersensitive sites have been identified at the promoters of the human alpha-like genes and within the region from 4 to 40 kb upstream of the gene cluster. One of these sites, HS-40, has been shown previously to be the major regulator of tissue-specific alpha-globin gene expression. We have now examined the function of other hypersensitive sites by studying the expression in mouse erythroleukemia (MEL) cells of various fragments containing these sites attached to HS-40 and an alpha-globin gene. High level expression of the alpha gene was observed in all cases. When clones of MEL cells bearing a single copy of the alpha-globin gene fragments were examined, expression levels were similar to those of the endogenous mouse alpha genes and similar to MEL cells bearing beta gene constructs under the control of the beta-globin locus control region. However, there was no evidence that the additional hypersensitive sites increased the level of expression or conferred copy number dependence on the expression of a linked alpha gene in MEL cells.
在人类α样基因的启动子以及基因簇上游4至40 kb区域内已鉴定出红系特异性脱氧核糖核酸酶I高敏位点。这些位点之一,即HS-40,先前已被证明是组织特异性α珠蛋白基因表达的主要调节因子。我们现在通过研究包含这些位点并与HS-40和一个α珠蛋白基因相连的各种片段在小鼠红白血病(MEL)细胞中的表达,来检测其他高敏位点的功能。在所有情况下均观察到α基因的高水平表达。当检测携带单拷贝α珠蛋白基因片段的MEL细胞克隆时,表达水平与内源性小鼠α基因的表达水平相似,并且与在β珠蛋白基因座控制区控制下携带β基因构建体的MEL细胞相似。然而,没有证据表明额外的高敏位点会增加MEL细胞中连接的α基因的表达水平或赋予其拷贝数依赖性。