Sheluho D, Yebra M J, Khariwala S S, Bhagwat A S
Wayne State University, Department of Chemistry, Detroit, MI 48202, USA.
Mol Gen Genet. 1997 Jun;255(1):54-9. doi: 10.1007/s004380050474.
The cytosine methyltransferases (MTases) M. HhaI and M. HpaII bind substrates in which the target cytosine is replaced by uracil or thymine, i.e. DNA containing a U:G or a T:G mismatch. We have extended this observation to the EcoRII MTase (M. EcoRII) and determined the apparent Kd for binding. Using a genetic assay we have also tested the possibility that MTase binding to U:G mismatches may interfere with repair of the mismatches and promote C:G to T:A mutations. We have compared two mutants of M. EcoRII that are defective for catalysis by the wild-type enzyme for their ability to bind DNA containing U:G or T:G mismatches and for their ability to promote C to T mutations. We find that although all three proteins are able to bind DNAs with mismatches, only the wild-type enzyme promotes C:G to T:A mutations in vivo. Therefore, the ability of M. EcoRII to bind U:G mismatched duplexes is not sufficient for their mutagenic action in cells.
胞嘧啶甲基转移酶(MTases)M. HhaI和M. HpaII结合的底物中,靶胞嘧啶被尿嘧啶或胸腺嘧啶取代,即含有U:G或T:G错配的DNA。我们已将这一观察结果扩展到EcoRII MTase(M. EcoRII)并确定了其结合的表观解离常数(Kd)。我们还使用遗传检测方法测试了MTase与U:G错配结合可能干扰错配修复并促进C:G到T:A突变的可能性。我们比较了M. EcoRII的两个突变体,它们对于野生型酶的催化作用有缺陷,比较它们结合含有U:G或T:G错配DNA的能力以及促进C到T突变的能力。我们发现,虽然所有这三种蛋白质都能够结合有错配的DNA,但只有野生型酶在体内促进C:G到T:A突变。因此,M. EcoRII结合U:G错配双链体的能力不足以使其在细胞中产生诱变作用。