Champoux J J
J Biol Chem. 1981 May 25;256(10):4805-9.
Conditions which result in DNA strand breakage by the rat liver DNA nicking-closing enzyme lead to the covalent attachment of the 3'-end of the broken strand to the enzyme. Treatment of this complex with pancreatic DNase leaves a residue of 17 +/- 8 nucleotide phosphates still attached to the enzyme. Subsequent nuclease P1 treatment removes all but 2 +/- 1 phosphate residues. Using nuclease P1-treated complexes which had been labeled in the DNA with 32P, the stability of the protein-DNA linkage was studied. The linkage is stable to acid, base, neutral and acidic hydroxylamine, and neutral I2. This pattern of stability rules out essentially all of the possible DNA-protein linkages except for a linkage involving a phosphodiester bond to the amino acid tyrosine. After acid hydrolysis of the 32P-labeled complexes, label was found to be associated with O4-phosphotyrosine, providing a direct demonstration that tyrosine is the amino acid to which the end of the DNA chain is attached.
由大鼠肝脏DNA切口-封闭酶导致DNA链断裂的情况会使断裂链的3'端与该酶发生共价连接。用胰DNA酶处理这种复合物后,仍有17±8个核苷酸磷酸残基附着在酶上。随后用核酸酶P1处理,除了2±1个磷酸残基外,其余的都被去除。使用在DNA中用32P标记的经核酸酶P1处理的复合物,研究了蛋白质-DNA连接的稳定性。该连接对酸、碱、中性和酸性羟胺以及中性I2都稳定。这种稳定性模式基本上排除了所有可能的DNA-蛋白质连接,除了涉及与氨基酸酪氨酸形成磷酸二酯键的连接。对32P标记的复合物进行酸水解后,发现标记与O4-磷酸酪氨酸相关,这直接证明酪氨酸是DNA链末端所连接的氨基酸。