Acuto S, Donovan-Peluso M, Giambona N, Bank A
Biochem Biophys Res Commun. 1987 Mar 30;143(3):1099-106. doi: 10.1016/0006-291x(87)90365-2.
Hybrid genes containing human gamma or beta globin gene promoters linked to a neomycin resistance (neoR) gene were transfected into erythroid (K562) and nonerythroid (HeLa) cells. The number of clones resistant to G418, a neomycin analogue, was used to assay promoter strength. The results indicate that in K562 cells both promoters are active, and the gamma gene promoter is much stronger than the beta. By contrast, neither gene promoter is active in HeLa cells. These experiments indicate that these globin gene promoters are tissue-specific and sufficient for activity.
将含有与新霉素抗性(neoR)基因相连的人γ或β珠蛋白基因启动子的杂种基因转染到红系(K562)和非红系(HeLa)细胞中。用对新霉素类似物G418有抗性的克隆数来测定启动子强度。结果表明,在K562细胞中,两种启动子均有活性,且γ基因启动子比β基因启动子活性强得多。相比之下,两种基因启动子在HeLa细胞中均无活性。这些实验表明,这些珠蛋白基因启动子具有组织特异性且足以发挥活性。