By Yujun George Zheng
Epigenetic Technological Applications is a compilation of state of the art applied sciences concerned with epigenetic learn. Epigenetics is an exhilarating new box of biology learn, and plenty of applied sciences are invented and built particularly for epigenetics examine. With chapters overlaying the newest advancements in crystallography, computational modeling, the makes use of of histones, and extra, Epigenetic Technological Applications addresses the query of ways those new principles, approaches, and concepts might be utilized to present epigenetics learn, and the way they could hold pushing discovery ahead and past the epigenetic realm.
- Discusses applied sciences which are severe for epigenetic study and application
- Includes epigenetic functions for cutting-edge technologies
- Contains an international viewpoint at the way forward for epigenetics
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Extra resources for Epigenetic Technological Applications
And Frommer et al. [34,35]. In these studies, which are often referenced as the beginning of the “bisulfite revolution,” sodium bisulfite was utilized to convert cytosine to uracil residues in denatured single-stranded DNA, while methylated cytosine residues, which are not reactive to sodium bisulfite, did not convert. The bisulfite conversion reaction is carried out through three steps with the first being sulphonation of cytosine, followed by hydrolytic deamination and subsequent alkali desulphonation, which yields the final product of uracil.
Lastly, methods such as TAB-Seq, OxBS-Seq, and Aba-Seq have been developed that can take advantage of next-generation sequencing to provide mapping of genome-wide 5mC or 5hmC at very high resolutions. It is the combination of all these technological advances, both past and present, which will provide the foundation and fuel the epigenetic revolution as we move forward. Furthermore, it is highly probable that new and unimaginable epigenetic tools will be proposed in the future that might completely change our perspective on mammalian epigenetic DNA modification.
Not surprisingly, after the development of these 5hmC antibodies, an ELISA-based method was proposed for the quantitative measurement of total genomic 5hmC. Since the 5mC and 5hmC modifications are structurally very similar there was some concern about the 5mC and 5hmC antibodies cross reactivity. Fortunately, a research group has recently reexamined the specificity of these antibodies and determined that they were indeed highly specific with little to no cross-reactivity . Enzymatic techniques were also developed for the measurement of either genomic 5mC or 5hmC [23,24].