Helland D E, Doetsch P W, Haseltine W A
Mol Cell Biol. 1986 Jun;6(6):1983-90. doi: 10.1128/mcb.6.6.1983-1990.1986.
The substrate specificity of a calf thymus endonuclease on DNA damaged by UV ligh, ionizing radiation, and oxidizing agents was investigated. End-labeled DNA fragments of defined sequence were used as substrates, and the enzyme-generated scission products were analyzed by using DNA sequencing methodologies. The enzyme was shown to incise damaged DNA at pyrimidine sites. The enzyme incised DNA damaged with UV light, ionizing radiation, osmium tetroxide, potassium permanganate, and hydrogen peroxide at cytosine and thymine sites. The substrate specificity of the calf thymus endonuclease was compared to that of Escherichia coli endonuclease III. Similar pyrimidine base damage specificities were found for both enzymes. These results define a highly conserved class of enzymes present in both procaryotes and eucaryotes that may mediate an important role in the repair of oxidative DNA damage.
研究了小牛胸腺核酸内切酶对紫外线、电离辐射和氧化剂损伤的DNA的底物特异性。将特定序列的末端标记DNA片段用作底物,并使用DNA测序方法分析酶产生的切割产物。结果表明,该酶在嘧啶位点切割受损DNA。该酶在胞嘧啶和胸腺嘧啶位点切割受紫外线、电离辐射、四氧化锇、高锰酸钾和过氧化氢损伤的DNA。将小牛胸腺核酸内切酶的底物特异性与大肠杆菌核酸内切酶III的底物特异性进行了比较。发现这两种酶具有相似的嘧啶碱基损伤特异性。这些结果确定了原核生物和真核生物中都存在的一类高度保守的酶,它们可能在氧化性DNA损伤的修复中起重要作用。