5HN2
Base Pairing and Structure Insights into the 5-Formylcytosine in RNA Duplex
5HN2 の概要
エントリーDOI | 10.2210/pdb5hn2/pdb |
分子名称 | RNA (5'-R(*GP*UP*AP*(OFC)P*GP*UP*AP*C)-3'), SODIUM ION (3 entities in total) |
機能のキーワード | rna, 5-formylcytosine |
由来する生物種 | synthetic construct |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 15350.42 |
構造登録者 | |
主引用文献 | Wang, R.,Luo, Z.,He, K.,Delaney, M.O.,Chen, D.,Sheng, J. Base pairing and structural insights into the 5-formylcytosine in RNA duplex. Nucleic Acids Res., 44:4968-4977, 2016 Cited by PubMed Abstract: 5-Formylcytidine (f(5)C), a previously discovered natural nucleotide in the mitochondrial tRNA of many species including human, has been recently detected as the oxidative product of 5-methylcytidine (m(5)C) through 5-hydroxymethylcytidine (hm(5)C) in total RNA of mammalian cells. The discovery indicated that these cytosine derivatives in RNA might also play important epigenetic roles similar as in DNA, which has been intensively investigated in the past few years. In this paper, we studied the base pairing specificity of f(5)C in different RNA duplex contexts. We found that the 5-formyl group could increase duplex thermal stability and enhance base pairing specificity. We present three high-resolution crystal structures of an octamer RNA duplex [5'-GUA(f(5)C)GUAC-3']2 that have been solved under three crystallization conditions with different buffers and pH values. Our results showed that the 5-formyl group is located in the same plane as the cytosine base and forms an intra-residue hydrogen bond with the amino group in the N4 position. In addition, this modification increases the base stacking between the f(5)C and the neighboring bases while not causing significant global and local structure perturbations. This work provides insights into the effects of 5-formylcytosine on RNA duplex. PubMed: 27079978DOI: 10.1093/nar/gkw235 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.5 Å) |
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