Farzaneh F, Meldrum R, Shall S
Nucleic Acids Res. 1987 Apr 24;15(8):3493-502. doi: 10.1093/nar/15.8.3493.
During the induced differentiation of the human promyelocytic leukaemic cell line, HL-60, along the myelocytic lineage, DNA strand-breaks are formed. These breaks which are formed in the face of a proficient DNA repair mechanism, are only transiently maintained and subsequently become religated. The ligation of these breaks requires the activity of the nuclear adenosine diphosphoribosyl transferase (ADPRT). Inhibition of nuclear ADPRT, an enzyme totally dependent on the presence of DNA strand-breaks for its activity and required for efficient DNA repair in eukaryotic cells, blocks the religation of these breaks but not their formation. The inhibition of DNA strand ligation in the differentiating HL-60 cells results in loss of viability and cell death.
在人早幼粒白血病细胞系HL-60沿髓细胞系诱导分化过程中,会形成DNA链断裂。这些断裂是在DNA修复机制完好的情况下形成的,只是暂时存在,随后会重新连接。这些断裂的连接需要核腺苷二磷酸核糖基转移酶(ADPRT)的活性。核ADPRT是一种完全依赖DNA链断裂的存在来发挥其活性的酶,也是真核细胞有效DNA修复所必需的,抑制该酶会阻断这些断裂的重新连接,但不会阻止其形成。对分化中的HL-60细胞DNA链连接的抑制会导致细胞活力丧失和细胞死亡。