By Nessa Carey (ed.)
Epigenetics is among the quickest relocating fields in drug discovery, with virtually each huge pharmaceutical corporation and a considerable variety of biotechnology businesses focusing on epigenetic tactics to regard ailments starting from melanoma to Huntington’s affliction and from irritation to sickle mobilephone anaemia.
The e-book is established in 3 major sections. the 1st part introduces epigenetics and clarify its significance at either a phenomenological and molecular point. the second one part is going directly to evaluation how all of the enormous breakthroughs in drug discovery during this box have constructed, with a robust emphasis on case histories. the ultimate part highlights the continuing demanding situations in developing secure and efficacious epigenetic drugs.
Written and edited by means of specialists in the box from either and academia, this booklet presents a useful advisor to this constructing box for medicinal chemists operating in academia and within the pharmaceutical industry.
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Additional info for Epigenetics for Drug Discovery
6 Epigenetic Crosstalk – Integrating Histone Modification and DNA Methylation A final topic is the level of integration between the different epigenetic processes. g. chromatin remodelling enzymes can be recruited by histone modifications), but also in long-term gene silencing via integration of DNA methylation with short-term histone modifications like acetylation and lysine methylation. This crosstalk is apparent in the mechanism of mark deposition, but also the ways the various marks impact on transcription.
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4 Mechanisms of histone crosstalk. Interactions between histones can have both positive and negative effects on the writing, reading and erasing processes. (A) Modification A (red mark) stimulates interactions with writers, readers and erasers of nearby modifications. (i) Modification A recruits the writer of mark C (yellow). (ii) Modification A stabilises the association of a reader protein with mark B (green), allowing recruitment of effector complexes. (iii) Modification A recruits an eraser of B.