期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 276, 期 51, 页码 48404-48409出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M108461200
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资金
- NIGMS NIH HHS [GMR01-59809, GMR01-17158] Funding Source: Medline
Endonuclease G (endoG) is released from mitochondria during apoptosis and is in part responsible for internucleosomal DNA cleavage. Here we report the action of the purified human recombinant form of this endonuclease on naked DNA and chromatin substrates. The addition of the protein to isolated nuclei from nonapoptotic cells first induces higher order chromatin cleavage into DNA fragments greater than or equal to 50 kb in length, followed by inter- and intranucleosomal DNA cleavages with products possessing significant internal single-stranded nicks spaced at nucleosomal (similar to 190 bases) and subnucleosomal (similar to 10 bases) periodicities. We demonstrate that both exonucleases and DNase I stimulate the ability of endoG to generate double-stranded DNA cleavage products at physiological ionic strengths, suggesting that these activities work in concert with endoG in apoptotic cells to ensure efficient DNA breakdown.
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