Lin C H, Palma J F, Solomon W B
Department of Medicine, Morse Institute for Molecular Biology and Genetics, State University of New York, Health Science Center at Brooklyn 11203.
Cell Mol Biol Res. 1994;40(1):13-26.
To understand how phorbol ester induction switches the leukemia cell line K562 from erythroid specific gene expression to an apparently irreversible program of megakaryocytic gene expression, we used a subtractive cDNA cloning strategy to identify cDNA sequence tags whose expression was suppressed after exposure of K562 cells to phorbol ester. The switch from the erythroid to megakaryocytic phenotype of K562 cells is due, at least in part, to marked decreases in the half-lives of erythroid specific mRNAs. The phorbol ester induced decreases in the half-lives of erythroid specific mRNAs is reversed by cycloheximide or an inhibitor of protein kinase C. The phorbol ester induced shut off of cell division, and apparent terminal differentiation and apoptosis of K562 cells is also associated with a coordinate decrease in the expression of mRNAs that encode ribosomal proteins.
为了理解佛波酯诱导如何使白血病细胞系K562从红系特异性基因表达转变为明显不可逆的巨核细胞基因表达程序,我们采用了消减cDNA克隆策略,以鉴定K562细胞暴露于佛波酯后其表达受到抑制的cDNA序列标签。K562细胞从红系表型向巨核细胞表型的转变至少部分是由于红系特异性mRNA半衰期的显著缩短。放线菌酮或蛋白激酶C抑制剂可逆转佛波酯诱导的红系特异性mRNA半衰期的缩短。佛波酯诱导的K562细胞分裂停止、明显的终末分化和凋亡也与编码核糖体蛋白的mRNA表达的协同下降有关。