Department of Chemistry, Sun Yat-Sen University , Guangzhou 510275, China.
Department of Chemistry and Institute for Biophysical Dynamics, Howard Hughes Medical Institute, The University of Chicago , Chicago, Illinois 60637, United States.
J Am Chem Soc. 2017 Oct 18;139(41):14436-14442. doi: 10.1021/jacs.7b06381. Epub 2017 Oct 3.
N-Methyladenine (N-mA or 6 mA) is an epigenetic DNA modification in eukaryotic genomes. In contrast to the well-established roles of 5-methylcytosine for epigenetic regulation of gene expression, the functional roles of N-mA remain elusive. In particular, the impact of N-mA modification of the DNA template on RNA polymerase II (pol II) transcription elongation is not known. In this work, using the Saccharomyces cerevisiae pol II transcriptional elongation system as a model, we investigated the molecular mechanism of pol II recognition and processing of N-mA sites via both biochemical and structural approaches. We found that N-mA causes site-specific pol II pausing/stalling. Structural analysis revealed that while N-mA can reach the +1 template position, the stability of the N-mA and UTP base pairing is compromised. Taken together, we reveal that the presence of the 6-methyl group on adenine reduces incorporation efficiency and promotes backtracking translocation. Our studies with yeast pol II provide molecular insights into understanding the impacts of N-mA on pol II transcription dynamics in different organisms.
N6-甲基腺嘌呤(N6-mA 或 6 mA)是真核基因组中的一种表观遗传 DNA 修饰。与 5-甲基胞嘧啶在基因表达的表观遗传调控中的成熟作用相比,N6-mA 的功能作用仍不清楚。特别是,N6-mA 修饰 DNA 模板对 RNA 聚合酶 II(pol II)转录延伸的影响尚不清楚。在这项工作中,我们使用酿酒酵母 pol II 转录延伸系统作为模型,通过生化和结构方法研究了 pol II 识别和处理 N6-mA 位点的分子机制。我们发现 N6-mA 导致 pol II 特异性暂停/stalling。结构分析表明,尽管 N6-mA 可以到达+1 模板位置,但 N6-mA 和 UTP 碱基配对的稳定性受到损害。总之,我们揭示了腺嘌呤上 6-甲基的存在降低了掺入效率并促进了回溯易位。我们对酵母 pol II 的研究提供了分子见解,有助于理解 N6-mA 对不同生物体内 pol II 转录动力学的影响。