One promising therapeutic approach for FA is to eliminate the root cause of the disease by contracting the expanded GAA repeat in the FXN gene using genome editing technologies. Genome editing technologies have revolutionized research by democratizing genetic changes and expanding our ability to make customizable modifications to the human genome. In this project, Dr Rufino-Ramos will explore a variety of CRISPR-based editing tools to contract the GAA repeats, which will correct the FXN defect and thereby restore frataxin expression. To minimize unwanted genetic modifications in other parts of the genome (called off-targets) by restricting the duration of expression of the genome editing tools, Dr Rufino-Ramos proposes to deliver these enzymes in a transient manner using cell derived vesicles, called extracellular vesicles (EVs). EVs encapsulate, protect, and permit targeting the CRISPR tools to the intended cells for a short period of time—long enough to contract the GAA repeats but short enough to minimize the risk of unwanted genome edits. Together, this research will explore safe and effective methods to treat FA through synergistic optimization of genome editing and delivery approaches.
Postdoctoral Fellowship | Gene & Stem Cell Therapy
Developing and delivering of novel gene editing technologies to contract GAA repeats in Friedreich’s ataxia
Grant Awarded | Mar 2024
David Rufino-Ramos, PhD
Harvard Medical School
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The FARA Grant Program is proud to award a Postdoctoral Fellowship to David Rufino-Ramos, PhD at Harvard Medical School to study the application of several CRISPR-derived editing tools to contract the GAA repeats.
Co-sponsor: fara Australia
LAY SUMMARY
Can we find new ways of removing the GAA repeats?
Related Research Publications
Click editing enables programmable genome writing using DNA polymerases and HUH endonucleases
Joana Ferreira da Silva, Connor J Tou, Emily M King, Madeline L Eller, David Rufino-Ramos, Linyuan Ma, Christopher R Cromwell, Jasna Metovic, Friederike M C Benning, Luke H Chao, Florian S Eichler, Benjamin P Kleinstiver