Bringing in the right combination of people with different perspectives and abilities can take a team to new heights. And just like that savvy diverse team, a new epigenome editing tool called the Spy-Snoop-Sun-Avi (SSSavi) system recruits diverse effector molecules in an interchangeable and orderly way to understand how combinations of DNA and histone modifications […]
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Search Results for: epigenetic editing
Epigenetic Inheritance During DNA Replication: A State Lying Somewhere Between Symmetry and Instability
Emerging research has provided evidence for the critical importance of the inheritance of epigenetic states, whether that be DNA methylation, histone modifications, or even non-coding RNAs. Now, three recent studies focusing on the mechanism involved in passing down this information from parental to daughter cells while they replicate their DNA and divide in vitro provide […]
“Dynamite” Study Uses TNT To Destroy Epigenetic Memories in Human iPSCs
While lingering memories can represent unwelcome guests, destroying them with the power of dynamite may seem like overkill! However, a volatile new study now describes TNT or transient-naïve-treatment as a simple means of ridding human induced pluripotent stem cells (hiPSC) of their epigenetic memories and improving their therapeutic potential. An explosive epigenetic team headed by […]
eBook: Epigenetics of Cancer & Disease Risk
The application of epigenetic approaches to disease research is moving quickly and hundreds of new papers are published every year, from virology to neurobiology and cancer. In this eBook, we present short summaries of interesting discoveries that caught our attention in each of these areas. Table of Contents Chapter 1: Epigenetics in Disease Risk Taking […]
Multiplexed Epigenome Editing Rouses a “Sleeping Dog” to Treat a Neurodevelopmental Disorder
“Let sleeping dogs lie” is sound advice for those who want to stay out of trouble! However, an eye-opening epigenome editing study now suggests that rousing the “sleeping” methyl CpG-binding protein 2 (MECP2) gene from the inactive X chromosome may represent a therapeutic opportunity for girls with Rett Syndrome – an X-linked neurodevelopmental disorder that […]