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通过化学标记结合质谱分析测定甲酰化 DNA 和 RNA。

Determination of formylated DNA and RNA by chemical labeling combined with mass spectrometry analysis.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.

出版信息

Anal Chim Acta. 2017 Aug 15;981:1-10. doi: 10.1016/j.aca.2017.06.009. Epub 2017 Jun 19.

Abstract

Nucleic acids carry diverse chemical modifications that exert critical influences in a variety of cellular processes in living organisms. In addition to methylation, the emerging DNA and RNA formylation has been reported to play functional roles in various physiological processes. However, the amounts of formylated DNA and RNA are extremely low and detection of DNA and RNA formylation is therefore a challenging task. To address this issue, we developed a strategy by chemical labeling combined with in-tube solid-phase microextraction - ultra high performance liquid chromatography - electrospray ionization - tandem mass spectrometry (in-tube SPME-UPLC-ESI-MS/MS) analysis for the sensitive determination of DNA and RNA formylation. Using the developed method, we were able to simultaneously measure six formylated nucleosides, including 5-formyl-2'-deoxycytidine (5-fodC), 5-formylcytidine (5-forC), 5-formyl-2'-deoxyuridine (5-fodU), 5-formyluridine (5-forU), 2'-O-methyl-5-formylcytidine (5-forCm) and 2'-O-methyl-5- formyluridine (5-forUm), from DNA and RNA of cultured human cells and multiple mammalian tissues. The detection limits of these formylated nucleosides improved by 307-884 folds using Girard's P (GirP) labeling coupled with in-tube SPME-UPLC-ESI-MS/MS analysis. It was worth noting that 5-forU, 5-forCm and 5-forUm which have not been detected in human sample before, were discovered in cultured human cells and tissues in the current study. In addition, we observed significant increase of 5-forC and 5-forU in RNA (p = 0.027 for 5-forC; p = 0.028 for 5-forU) and 5-fodU in DNA (p = 0.002) in human thyroid carcinoma tissues compared to normal tissues adjacent to the tumor using synthesized stable isotope GirP (d-GirP)-assisted quantification. Our results indicated that aberrant DNA and RNA formylation may contribute to the tumor formation and development. In addition, monitoring of DNA and RNA formylation may also serve as indicator for cancer diagnostics. Taken together, the developed chemical labeling combined with in-tube SPME-UPLC-ESI-MS/MS analysis can facilitate the in-depth functional study of DNA and RNA formylation.

摘要

核酸携带多种化学修饰,这些修饰在生物体的各种细胞过程中发挥着关键影响。除了甲基化之外,新兴的 DNA 和 RNA 甲酰化已被报道在各种生理过程中发挥功能作用。然而,甲酰化 DNA 和 RNA 的含量极低,因此检测 DNA 和 RNA 甲酰化是一项具有挑战性的任务。为了解决这个问题,我们开发了一种化学标记结合管内固相微萃取-超高效液相色谱-电喷雾电离-串联质谱(in-tube SPME-UPLC-ESI-MS/MS)分析的策略,用于灵敏地测定 DNA 和 RNA 甲酰化。使用所开发的方法,我们能够同时测量来自培养的人类细胞和多种哺乳动物组织的 DNA 和 RNA 中的六种甲酰化核苷,包括 5-甲酰基-2'-脱氧胞苷(5-fodC)、5-甲酰胞苷(5-forC)、5-甲酰基-2'-脱氧尿苷(5-fodU)、5-甲酰尿苷(5-forU)、2'-O-甲基-5-甲酰胞苷(5-forCm)和 2'-O-甲基-5-甲酰尿苷(5-forUm)。使用 Girard 的 P(GirP)标记结合管内固相微萃取-超高效液相色谱-电喷雾电离-串联质谱分析,这些甲酰化核苷的检测限提高了 307-884 倍。值得注意的是,以前在人类样本中未检测到的 5-forU、5-forCm 和 5-forUm 在本研究中在培养的人类细胞和组织中被发现。此外,与肿瘤相邻的正常组织相比,我们观察到人类甲状腺癌组织中 RNA 中的 5-forC 和 5-forU(5-forC 的 p=0.027;5-forU 的 p=0.028)和 DNA 中的 5-fodU(p=0.002)显著增加,使用合成的稳定同位素 GirP(d-GirP)辅助定量。我们的结果表明,异常的 DNA 和 RNA 甲酰化可能有助于肿瘤的形成和发展。此外,DNA 和 RNA 甲酰化的监测也可以作为癌症诊断的指标。总之,开发的化学标记结合管内固相微萃取-超高效液相色谱-电喷雾电离-串联质谱分析可以促进对 DNA 和 RNA 甲酰化的深入功能研究。

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