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DNA中天然T修饰的选择性化学标记

Selective Chemical Labeling of Natural T Modifications in DNA.

作者信息

Hardisty Robyn E, Kawasaki Fumiko, Sahakyan Aleksandr B, Balasubramanian Shankar

机构信息

†Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

‡Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, U.K.

出版信息

J Am Chem Soc. 2015 Jul 29;137(29):9270-2. doi: 10.1021/jacs.5b03730. Epub 2015 May 12.

Abstract

We present a chemical method to selectively tag and enrich thymine modifications, 5-formyluracil (5-fU) and 5-hydroxymethyluracil (5-hmU), found naturally in DNA. Inherent reactivity differences have enabled us to tag 5-fU chemoselectively over its C modification counterpart, 5-formylcytosine (5-fC). We rationalized the enhanced reactivity of 5-fU compared to 5-fC via ab initio quantum mechanical calculations. We exploited this chemical tagging reaction to provide proof of concept for the enrichment of 5-fU containing DNA from a pool that contains 5-fC or no modification. We further demonstrate that 5-hmU can be chemically oxidized to 5-fU, providing a strategy for the enrichment of 5-hmU. These methods will enable the mapping of 5-fU and 5-hmU in genomic DNA, to provide insights into their functional role and dynamics in biology.

摘要

我们提出了一种化学方法,用于选择性标记和富集天然存在于DNA中的胸腺嘧啶修饰——5-甲酰基尿嘧啶(5-fU)和5-羟甲基尿嘧啶(5-hmU)。固有的反应性差异使我们能够在其C修饰对应物5-甲酰基胞嘧啶(5-fC)上对5-fU进行化学选择性标记。我们通过从头算量子力学计算,阐明了5-fU与5-fC相比反应性增强的原因。我们利用这种化学标记反应,为从含有5-fC或无修饰的混合物中富集含5-fU的DNA提供了概念验证。我们进一步证明,5-hmU可以被化学氧化为5-fU,从而提供了一种富集5-hmU的策略。这些方法将能够对基因组DNA中的5-fU和5-hmU进行定位,从而深入了解它们在生物学中的功能作用和动态变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cb5/4521287/4e6744fba0b2/ja-2015-03730t_0001.jpg

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