Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain
the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in
Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles
and JavaScript.
DNA base editors are promising tools that can induce point mutations at desired sites in the genome. However, a major limitation in applying such systems is the prerequisite of a protospacer adjacent motif (PAM) sequence next to the target site. In a News and Views, Pratishtha Varshney and Gaurav Varshney discuss how SpRY-based DNA base editors, with highly flexible PAM recognition, greatly expand targetable sites in the genome and the possibilities for disease modeling in zebrafish.
The application of genome-editing tools to generate point mutations in animal models is of particular value for precise disease modeling, but the PAM requirement of Cas enzymes is a critical limiting factor. Two new studies demonstrate that SpRY variant displays efficient genome editing in a nearly PAM-less manner in zebrafish, expanding the targeting scope of base editors in this model.
A challenge in translational research is comparing behaviors across species. A new study combines a novel behavioral paradigm in rats and humans with reinforcement learning to infer shared computations for goal-directed navigation.
Rats undergoing the stress-enhanced fear learning procedure are usually housed in social isolation and exposed to a trauma-like experience of 15 massed electric footshocks. By showing that group-housed rats receiving fewer and lower-magnitude electric shocks still exhibit PTSD-relevant changes, this new study presents refinements of the procedure to reduce potential animal pain.