Plumb M, Frampton J, Wainwright H, Walker M, Macleod K, Goodwin G, Harrison P
Beatson Institute for Cancer Research, Glasgow, UK.
Nucleic Acids Res. 1989 Jan 11;17(1):73-92. doi: 10.1093/nar/17.1.73.
An erythroid-specific nuclear protein factor binds to a sequence motif (GATAAG) which is present in the promoter region of the mouse alpha and beta major globin genes, and in the erythroid-specific promoter of the human porphobilinogen deaminase (PBG-D) gene. The protein activity is conserved across species, being found in mouse erythroleukaemia (MEL) cells, chicken erythrocytes, the human erythroid K562 and KMOE cell lines, but not in a variety of non-erythroid mouse tissues or in HeLa cells. Functional analysis of this element in the alpha globin gene promoter by stable transfection experiments show that the GATAAG motif resides in a 68 bp sequence which has a stimulatory effect on transcription in mouse erythroleukaemia but not fibroblast cells. The GATAAG motif is conserved in the promoters and 3' enhancers of a variety of globin and non-globin genes implying that it is a cis-element involved in the tissue-specific up-regulation of several genes that are co-expressed during erythroid cell differentiation.
一种红系特异性核蛋白因子与一个序列基序(GATAAG)结合,该基序存在于小鼠α和β主要珠蛋白基因的启动子区域以及人胆色素原脱氨酶(PBG-D)基因的红系特异性启动子中。这种蛋白质活性在物种间保守,在小鼠红白血病(MEL)细胞、鸡红细胞、人红系K562和KMOE细胞系中存在,但在多种非红系小鼠组织或HeLa细胞中不存在。通过稳定转染实验对α珠蛋白基因启动子中该元件进行功能分析表明,GATAAG基序位于一个68 bp的序列中,该序列对小鼠红白血病细胞而非成纤维细胞中的转录有刺激作用。GATAAG基序在多种珠蛋白和非珠蛋白基因的启动子和3'增强子中保守,这意味着它是一个顺式元件,参与了红系细胞分化过程中几个共表达基因的组织特异性上调。