Mi S, Roberts R J
Cold Spring Harbor Laboratory, NY 11724.
Nucleic Acids Res. 1992 Sep 25;20(18):4811-6. doi: 10.1093/nar/20.18.4811.
The HpaII methylase (M.HpaII) recognizes the sequence CCGG and methylates the inner cytosine residue. The MspI methylase (MspI) recognizes the same sequence but methylates the outer cytosine residue. Both methylases have the usual architecture of 10 well-conserved motifs surrounding a variable region, responsible for sequence specific recognition, that is quite different in the two methylases. We have constructed hybrids between these two methylases and studied their methylation properties. A hybrid containing the variable region and C-terminal sequences from M.MspI methylates the outer cytosine residue. A second hybrid identical to the first except that the variable region derives from the M.HpaII methylates the inner cytosine residue. Thus the choice of base to be methylated within the recognition sequence is determined by the variable region.
HpaII甲基化酶(M.HpaII)识别序列CCGG并使内部胞嘧啶残基甲基化。MspI甲基化酶(MspI)识别相同序列,但使外部胞嘧啶残基甲基化。两种甲基化酶都具有围绕可变区的10个保守基序的常见结构,该可变区负责序列特异性识别,在两种甲基化酶中差异很大。我们构建了这两种甲基化酶之间的杂种并研究了它们的甲基化特性。一种包含来自M.MspI可变区和C端序列的杂种使外部胞嘧啶残基甲基化。第二个杂种与第一个相同,只是可变区源自M.HpaII,它使内部胞嘧啶残基甲基化。因此,识别序列内要甲基化的碱基选择由可变区决定。