Related Experiment Video
Updated: Jun 30, 2025

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
Published on: March 31, 2022
Developmental progression of DNA double-strand break repair deciphered by a single-allele resolution mutation
Zhiqian Li1,2, Lang You1,2, Anita Hermann1,2
1Department of Cell and Developmental Biology, University of California, San Diego, La Jolla, CA, 92093, USA.
Abstract:
DNA double-strand breaks (DSBs) are repaired by a hierarchically regulated network of pathways. Factors influencing the choice of particular repair pathways, however remain poorly characterized. Here we develop an Integrated Classification Pipeline (ICP) to decompose and categorize CRISPR/Cas9 generated mutations on genomic target sites in complex multicellular insects. The ICP outputs graphic rank ordered classifications of mutant alleles to visualize discriminating DSB repair fingerprints generated from different target sites and alternative inheritance patterns of CRISPR components. We uncover highly reproducible lineage-specific mutation fingerprints in individual organisms and a developmental progression wherein Microhomology-Mediated End-Joining (MMEJ) or Insertion events predominate during early rapid mitotic cell cycles, switching to distinct subsets of Non-Homologous End-Joining (NHEJ) alleles, and then to Homology-Directed Repair (HDR)-based gene conversion. These repair signatures enable marker-free tracking of specific mutations in dynamic populations, including NHEJ and HDR events within the same samples, for in-depth analysis of diverse gene editing events.
Related Concept Videos
Fixing Double-strand Breaks
Homologous Recombination
Long-patch Base Excision Repair
Mismatch Repair
Base Excision Repair
The first step of...
Restarting Stalled Replication Forks

