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Updated: Dec 20, 2025

Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors
Published on: February 28, 2021
A dual-deaminase CRISPR base editor enables concurrent adenine and cytosine editing
Julian Grünewald1,2,3, Ronghao Zhou1,2, Caleb A Lareau1,4
1Molecular Pathology Unit, Massachusetts General Hospital, Charlestown, MA, USA.
Abstract:
Existing adenine and cytosine base editors induce only a single type of modification, limiting the range of DNA alterations that can be created. Here we describe a CRISPR-Cas9-based synchronous programmable adenine and cytosine editor (SPACE) that can concurrently introduce A-to-G and C-to-T substitutions with minimal RNA off-target edits. SPACE expands the range of possible DNA sequence alterations, broadening the research applications of CRISPR base editors.
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