Kimber Scott T, Brown Tom, Fox Keith R
Centre for Biological Sciences, University of Southampton, Highfield, Southampton, United Kingdom.
Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Oxford, United Kingdom.
PLoS One. 2014 Apr 16;9(4):e95394. doi: 10.1371/journal.pone.0095394. eCollection 2014.
We demonstrate that a mutant of uracil DNA glycosylase (N123D:L191A) distinguishes between cytosine and methylcytosine. Uracil DNA glycosylase (UDG) efficiently removes uracil from DNA in a reaction in which the base is flipped into the enzyme's active site. Uracil is selected over cytosine by a pattern of specific hydrogen bonds, and thymine is excluded by steric clash of its 5-methyl group with Y66. The N123D mutation generates an enzyme that excises cytosine. This N123D:L191A mutant excises C when it is mispaired with A or opposite an abasic site, but not when it is paired with G. In contrast no cleavage is observed with any substrates that contain 5-methylcytosine. This enzyme may offer a new approach for discriminating between cytosine and 5-methylcytosine.
我们证明,尿嘧啶DNA糖基化酶的一种突变体(N123D:L191A)能够区分胞嘧啶和5-甲基胞嘧啶。尿嘧啶DNA糖基化酶(UDG)可在一种将碱基翻转到酶活性位点的反应中有效地从DNA中去除尿嘧啶。通过特定氢键模式,尿嘧啶比胞嘧啶更易被选择,而胸腺嘧啶因其5-甲基与Y66的空间冲突而被排除在外。N123D突变产生了一种可切除胞嘧啶的酶。这种N123D:L191A突变体在与A错配或与无碱基位点相对时切除C,但与G配对时则不切除。相比之下,对于任何含有5-甲基胞嘧啶的底物均未观察到切割现象。这种酶可能为区分胞嘧啶和5-甲基胞嘧啶提供一种新方法。