Goffin C, Verly W G
Biochem J. 1984 May 15;220(1):133-7. doi: 10.1042/bj2200133.
DNA from T7 phage containing AP (apurinic/apyrimidinic) sites was repaired by the successive actions of three chromatin enzymes [AP endodeoxyribonuclease, DNAase IV (5'----3'-exodeoxyribonuclease) and DNA polymerase-beta] prepared from rat liver and T4-phage DNA ligase. Since DNA ligase is also found in rat liver chromatin, all the activities used for the successful repair in vitro are thus present in the chromatin of a eukaryotic cell. Our results show, in particular, that the chromatin DNAase IV is capable of excising the AP site from the DNA strand nicked by the chromatin AP endodeoxyribonuclease. We did not try to combine all the enzymes, since competition between some of them might have prevented the repair; we have, for instance, shown that DNA ligase can seal the incision 5' to the AP site made by the AP endodeoxyribonuclease. Changes in chromatin structure during repair might perhaps prevent this competition when nuclear DNA is repaired in the living cell.
来自含有脱嘌呤/脱嘧啶(AP)位点的T7噬菌体的DNA,可通过由大鼠肝脏制备的三种染色质酶[AP内切脱氧核糖核酸酶、DNA酶IV(5'→3'外切脱氧核糖核酸酶)和DNA聚合酶β]以及T4噬菌体DNA连接酶的连续作用进行修复。由于在大鼠肝脏染色质中也发现了DNA连接酶,因此体外成功修复所使用的所有活性都存在于真核细胞的染色质中。我们的结果特别表明,染色质DNA酶IV能够从被染色质AP内切脱氧核糖核酸酶切割的DNA链上切除AP位点。我们没有尝试将所有酶组合起来,因为其中一些酶之间的竞争可能会阻止修复;例如,我们已经表明,DNA连接酶可以封闭由AP内切脱氧核糖核酸酶在AP位点5'端形成的切口。修复过程中染色质结构的变化可能会在活细胞中修复核DNA时阻止这种竞争。