4.7 Review

Detection of Genomic Uracil Patterns

期刊

出版社

MDPI
DOI: 10.3390/ijms22083902

关键词

uracil-DNA; dot blot; in situ detection; PCR-based U-DNA detection; genome-wide uracil mapping

资金

  1. National Research, Development and Innovation Office of Hungary [K 119493, NKP-2018-1.2.1-NKP-2018-00005]
  2. BME-Biotechnology FIKP grant of EMMI (BME FIKP-BIO)

向作者/读者索取更多资源

The appearance of uracil in DNA is a common genomic modification, with three different routes of formation, two of which do not require specific enzymes. Efficient uracil-DNA detection methods are crucial to understanding the potential roles of genomic uracil.
The appearance of uracil in the deoxyuridine moiety of DNA is among the most frequently occurring genomic modifications. Three different routes can result in genomic uracil, two of which do not require specific enzymes: spontaneous cytosine deamination due to the inherent chemical reactivity of living cells, and thymine-replacing incorporation upon nucleotide pool imbalances. There is also an enzymatic pathway of cytosine deamination with multiple DNA (cytosine) deaminases involved in this process. In order to describe potential roles of genomic uracil, it is of key importance to utilize efficient uracil-DNA detection methods. In this review, we provide a comprehensive and critical assessment of currently available uracil detection methods with special focus on genome-wide mapping solutions. Recent developments in PCR-based and in situ detection as well as the quantitation of genomic uracil are also discussed.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据