Method Article

CRISPR-Mediated Base Editing Tools: A Genome Editing Technique to Induce Targeted Base Substitution

July 8th, 2025

In This Article

Abstract

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Source: See, J. E., et al. Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors. J. Vis. Exp. (2021).

This video explains the concept of CRISPR-mediated cytosine base editors for inducing targeted nucleotide substitution.

Protocol

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1. Creation of BRCA1 variants using CRISPR-mediated base editing tools

NOTE: If HAP1-BE3 cell lines is not used, BE3-encoding plasmid DNA can be co-transfected with BRCA1-targeting gRNA. Compared to co-transfection of BE3 and gRNA plasmids, transfection of gRNA plasmid to HAP-BE3 cells induce efficient base editing up to 3-fold at target locus in our hands.

  1. Seed 5 x 105 HAP1-BE3 cells (or HAP1 cells in case of co-transfection methods) per well in 24-well plates 1 day prior to transfection. At the time of transfection, culture cells to reach an appropriate density (70%–80% confluence).
  2. Transfect BRCA1-targeting gRNAs using the purchased transfection reagents (Table of Materials) according to the manufacturer’s protocol. Use 1 µg of BRCA1-targeting gRNAs (with 1 µg of BE3-encoding plasmid DNA in case of co-transfection methods) to induce C:G to T:A conversion at BRCA1 target sites. Incubate the cells at 37 °C and subculture every 3–4 days.
  3. Harvest the cell pellets 3, 10, and 24 days after transfection to analyze base editing efficiencies (Samples from 3 days after transfection are analyzed regrading as day 0 samples).
  4. Extract genomic DNA using the genomic DNA purification kit (Table of Materials).
    NOTE: We recommend optimizing transfection conditions with variable ratio of reagent to DNA. Optimal condition for HAP1 transfection is 4:1 ration of reagent to DNA in our hands.

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Lipofectamine 2000 Thermo Fisher Scientific 11668027Transfection reagent
Opti-MEM Gibco 31985070Transfection materials
FuGENE HD Transfection Reagent Promega E2311 Transfection reagent
Iscove’s modified Dulbecco’s medium Gibco 12440046Medium for HAP1 cells
lentiCas9-Blast Addgene 52962Plasmids DNA for lentiBE3 cloning
DNeasy Blood & Tissue KitQiagen69504Genomic DNA prep. kit

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Tags

CRISPR Base EditingCytosine Base EditorBRCA1 Gene TargetingGuide RNA DesignLentiviral TransfectionGenomic DNA ExtractionBase Editing EfficiencyHAP1 BE3 CellsCas9 EndonucleaseCytidine Deaminase

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