Sauerbier W
Biochem Biophys Res Commun. 1986 Nov 26;141(1):204-12. doi: 10.1016/s0006-291x(86)80355-2.
T4 UV endonuclease cleaves double- and single-stranded DNA with equal specificity for photo-pyrimidine dimers. Thus, the enzyme can be used for mapping and quantifying pyrimidine dimers in single-stranded DNA as well as in double-stranded DNA. Mapping of pyrimidine dimers shows that rates of UV-dimerization are not only affected by 5', 3' adjacent bases, but also by position within pyrimidine tracts. Di-pyrimidines at 3' ends of tracts are more photoreactive than those at 5' ends.
T4紫外线内切核酸酶对光嘧啶二聚体具有同等特异性地切割双链和单链DNA。因此,该酶可用于绘制和定量单链DNA以及双链DNA中的嘧啶二聚体。嘧啶二聚体的图谱显示,紫外线二聚化速率不仅受5'、3'相邻碱基的影响,还受嘧啶序列内位置的影响。序列3'端的二嘧啶比5'端的二嘧啶更具光反应性。