Haukanes B I, Helland D E, Kleppe K
Laboratory of Biotechnology, University of Bergen, Norway.
Nucleic Acids Res. 1989 Feb 25;17(4):1493-509. doi: 10.1093/nar/17.4.1493.
An apurinic/apyrimidinic (AP) specific endonuclease from mouse plasmacytoma cells (line MPC-11), was observed to cleave apurinic sites in oligonucleotides 9, 11, 12, 39 and 40 nucleotides in length. However, the enzyme failed to cleave AP-sites in two oligonucleotides 7 nucleotides in length. The maximum rates of digestion observed on these short single-stranded DNA (ssDNA) fragments were approximately 1/30 of the rates observed on double-stranded DNA (dsDNA). In studies using the Maxam-Gilbert DNA sequencing analysis, apurinic sites in purine-rich regions were preferentially cleaved in dsDNA but not in ssDNA, indicating that the enzyme has a sequence preference on dsDNA. These results suggest that some sites on DNA might be more efficiently repaired than others.
从小鼠浆细胞瘤细胞(MPC - 11系)中分离出的一种脱嘌呤/脱嘧啶(AP)特异性内切核酸酶,可切割长度为9、11、12、39和40个核苷酸的寡核苷酸中的脱嘌呤位点。然而,该酶无法切割两种长度为7个核苷酸的寡核苷酸中的AP位点。在这些短单链DNA(ssDNA)片段上观察到的最大消化速率约为双链DNA(dsDNA)上观察到的速率的1/30。在使用Maxam - Gilbert DNA测序分析的研究中,富含嘌呤区域的脱嘌呤位点在dsDNA中被优先切割,而在ssDNA中则不会,这表明该酶对dsDNA具有序列偏好性。这些结果表明,DNA上的某些位点可能比其他位点更容易被修复。