Widłak P
Department of Experimental and Clinical Radiobiology, Center of Oncology, Gliwice, Poland.
Acta Biochim Pol. 2000;47(4):1037-44.
The sequential generation of large-scale DNA fragments followed by internucleosomal chromatin fragmentation is a biochemical hallmark of apoptosis. One of the nucleases primarily responsible for genomic DNA fragmentation during apoptosis is called DNA Fragmentation Factor 40 (DFF40) or Caspase-activated DNase (CAD). DFF40/CAD is a magnesium-dependent endonuclease specific for double stranded DNA that generates double strand breaks with 3'-hydroxyl ends. DFF40/CAD is activated by caspase-3 that cuts the nuclease's inhibitor DFF45/ICAD. The nuclease preferentially attacks chromatin in the internucleosomal linker DNA. However, the nuclease hypersensitive sites can be detected and DFF40/CAD is potentially involved in large-scale DNA fragmentation as well. DFF40/CAD-mediated DNA fragmentation triggers chromatin condensation that is another hallmark of apoptosis.
大规模DNA片段的顺序生成,随后是核小体间染色质片段化,是细胞凋亡的生化标志。在细胞凋亡过程中,主要负责基因组DNA片段化的核酸酶之一称为DNA片段化因子40(DFF40)或半胱天冬酶激活的脱氧核糖核酸酶(CAD)。DFF40/CAD是一种依赖镁的双链DNA特异性内切核酸酶,可产生具有3'-羟基末端的双链断裂。DFF40/CAD由切割核酸酶抑制剂DFF45/ICAD的半胱天冬酶-3激活。该核酸酶优先攻击核小体间连接DNA中的染色质。然而,核酸酶超敏位点也可以被检测到,并且DFF40/CAD也可能参与大规模DNA片段化。DFF40/CAD介导的DNA片段化触发染色质凝聚,这是细胞凋亡的另一个标志。