Unconstrained genome targeting with near-PAMless engineered CRISPR-Cas9 variants
Author(s) -
Russell T. Walton,
Kathleen A. Christie,
Madelynn N. Whittaker,
Benjamin P. Kleinstiver
Publication year - 2020
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aba8853
Subject(s) - crispr , cas9 , nuclease , genome editing , computational biology , genome engineering , genome , biology , dna , limiting , genetics , gene , mechanical engineering , engineering
A PAMless base editor CRISPR-Cas DNA base editing typically requires a specific motif for targeting known as a protospacer-adjacent motif (PAM). This requirement limits the sequences within a genome that can be targeted. Waltonet al. engineered specific variants of theStreptococcus pyogenes Cas9 enzyme named SpG and SpRY that could recognize and edit a wider array of PAMs. Using SpRY, the authors were able to correct previously uneditable mutations associated with human disease. Although off-target effects were observed for these engineered Cas enzymes at levels similar to those of the wild-type enzyme, depending on the context, these engineered enzymes widen the potential applications of precision genome editing.Science , this issue p.290
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom