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Inducible DNA Demethylation Mediated by the Maize Suppressor-mutator Transposon-Encoded TnpA Protein

机译:玉米抑制子-突变体转座子编码的TnpA蛋白介导的诱导型DNA去甲基化。

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摘要

Heritable epigenetic inactivation of the maize Suppressor-mutator (Spm) transposon is associated with promoter methylation, and its reversal is mediated by the transposon-encoded TnpA protein. We have developed an assay that permits demethylation of the Spm sequence to be controlled by inducing the expression of TnpA in plant cells. Using this assay, we show that demethylation is a rapid, active process. TnpA is a weak transcriptional activator, and deletions that abolish its transcriptional activity also eliminate its demethylation activity. We show that cell cycle and DNA synthesis inhibitors interfere with TnpA-mediated Spm demethylation. We further show that TnpA has a much lower affinity for fully methylated than for hemimethylated or unmethylated DNA fragments derived from Spm termini. Based on these observations, we suggest that TnpA binds to the postreplicative, hemimethylated Spm sequence and promotes demethylation either by creating an appropriate demethylation substrate or by itself participating in or recruiting a demethylase.
机译:玉米抑制子-突变体(Spm)转座子的可遗传表观遗传失活与启动子甲基化有关,其逆转由转座子编码的TnpA蛋白介导。我们已经开发出一种测定方法,该方法可以通过诱导植物细胞中TnpA的表达来控制Spm序列的去甲基化。使用该测定法,我们表明去甲基化是一个快速,活跃的过程。 TnpA是一种弱转录激活因子,废除其转录活性的缺失也消除了其去甲基化活性。我们表明细胞周期和DNA合成抑制剂干扰TnpA介导的Spm去甲基化。我们进一步表明,TnpA对完全甲基化的亲和力比对源自Spm末端的半甲基化或未甲基化的DNA片段的亲和力低得多。基于这些观察结果,我们建议TnpA与复制后的半甲基化Spm序列结合,并通过创建合适的脱甲基底物或自身参与或募集脱甲基酶来促进脱甲基。

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