Yamamoto T, Matsui Y, Natori S, Obinata M
Department of Cell Biology, Tohoku University, Sendai, Japan.
Gene. 1989 Aug 15;80(2):337-43. doi: 10.1016/0378-1119(89)90297-7.
DNA complementary to mRNA preferentially produced in murine erythroleukemia (MEL) cells was cloned from a cDNA library of anemic mouse spleen mRNAs. An open reading frame was noted in the cloned DNA, and was tentatively designated MER5. The MER5 mRNA is abundant in three MEL cell lines, but less in other tissues or cell lines. The levels of the MER5 mRNA changed periodically during MEL cell differentiation and decreased as globin mRNA accumulated. The MER5 promoter region contained no typical TATA-like sequence, but possible target sequences for AP1, AP2, SP1 and octamer-binding protein. More interestingly, this promoter contained the duplicated CACCC boxes, which are common in the adult beta-globin promoter from many species, but uncommon for promoters of other eukaryotic genes.
从小鼠贫血脾脏mRNA的cDNA文库中克隆出与在鼠红细胞白血病(MEL)细胞中优先产生的mRNA互补的DNA。在克隆的DNA中发现了一个开放阅读框,并暂时命名为MER5。MER5 mRNA在三种MEL细胞系中含量丰富,但在其他组织或细胞系中含量较少。在MEL细胞分化过程中,MER5 mRNA的水平周期性变化,并随着珠蛋白mRNA的积累而降低。MER5启动子区域不包含典型的TATA样序列,但含有AP1、AP2、SP1和八聚体结合蛋白的可能靶序列。更有趣的是,该启动子包含重复的CACCC框,这在许多物种的成人β-珠蛋白启动子中很常见,但在其他真核基因的启动子中并不常见。