首页> 外文期刊>Nucleic Acids Research >ROS1 5-methylcytosine DNA glycosylase is a slow-turnover catalyst that initiates DNA demethylation in a distributive fashion.
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ROS1 5-methylcytosine DNA glycosylase is a slow-turnover catalyst that initiates DNA demethylation in a distributive fashion.

机译:ROS1 5-甲基胞嘧啶DNA糖基化酶是一种缓慢翻转的催化剂,可以以分布方式引发DNA脱甲基。

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Arabidopsis ROS1 belongs to a family of plant 5-methycytosine DNA glycosylases that initiate DNA demethylation through base excision. ROS1 displays the remarkable capacity to excise 5-meC, and to a lesser extent T, while retaining the ability to discriminate effectively against C and U. We found that replacement of the C5-methyl group by halogen substituents greatly decreased excision of the target base. Furthermore, 5-meC was excised more efficiently from mismatches, whereas excision of T only occurred when mispaired with G. These results suggest that ROS1 specificity arises by a combination of selective recognition at the active site and thermodynamic stability of the target base. We also found that ROS1 is a low-turnover catalyst because it binds tightly to the abasic site left after 5-meC removal. This binding leads to a highly distributive behaviour of the enzyme on DNA substrates containing multiple 5-meC residues, and may help to avoid generation of double-strand breaks during processing of bimethylated CG dinucleotides. We conclude that the biochemical properties of ROS1 are consistent with its proposed role in protecting the plant genome from excess methylation.
机译:拟南芥ROS1属于植物5-甲基胞嘧啶DNA糖基化酶家族,可通过碱基切除引发DNA脱甲基。 ROS1显示出显着的切除5-meC的能力,并在较小的范围内表现出T,同时保留了有效区分C和U的能力。我们发现用卤素取代基取代C5-甲基大大降低了目标碱基的切除。此外,从错配中更有效地切除了5-meC,而T的切除仅在与G错配时发生。这些结果表明,ROS1特异性是由活性位点的选择性识别和靶碱基的热力学稳定性共同产生的。我们还发现ROS1是一种低周转率的催化剂,因为它与5-meC去除后紧密结合到剩下的无碱基位点。这种结合导致了该酶在含有多个5-meC残基的DNA底物上的高度分布行为,并可能有助于避免在双甲基化CG二核苷酸加工过程中产生双链断裂。我们得出结论,ROS1的生化特性与其在保护植物基因组免受过量甲基化的作用中所提出的作用是一致的。

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