Base Editing Efficiency

Base editing efficiency is the proportion of intended DNA base changes produced by a base editor at a target site, making it a key measure of precision and performance in genome engineering. In this CRISPR-based technique, a guide RNA directs a catalytically modified Cas protein to a complementary sequence, positioning a deaminase to convert cytosine to thymine or adenine to guanine without creating a double-strand DNA break. Efficiency depends on the editor, guide sequence, genomic location, delivery method, and cell type, while bystander edits can affect outcomes. Measuring it supports optimization for functional genomics, disease modeling, and potential therapeutic development.

Base Editing Efficiency - Related Videos

Research

JoVE EoE - Genome Editing Techniques

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

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2025

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

Education

JoVE Science Education - Advanced Biology

Genome Editing

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2023

A well-established technique for modifying specific sequences in the genome is gene targeting by homologous recombination, but this method can be laborious and only works in certain organisms. Recent advances have led to the development of “genome editing”, which works by inducing double-strand breaks in DNA using engineered nuclease enzymes guided to target genomic sites by either proteins or RNAs that recognize specific sequences. When a cell attempts to repair this damage, mutations can be...

Improved Genome Editing via Oviductal Nucleic Acids Delivery-based In Vivo Electroporation Technique for Knockout Mice Generation

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2025

The efficiency of the Improved Genome Editing via Oviductal Nucleic Acids Delivery (I-GONAD) method is comparable to traditional microinjection, which requires zygote collection from donor females and transfer to pseudo-pregnant females. This protocol demonstrates its effectiveness by introducing CRISPR/Cas9-induced mutations into the ROSA26 locus on chromosome 6.

Efficient Generation and Editing of Feeder-free IPSCs from Human Pancreatic Cells Using the CRISPR-Cas9 System

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Cited by 4 •

2017

This protocol describes in detail the generation of footprint-free induced pluripotent stem cells (iPSCs) from human pancreatic cells in feeder-free conditions, followed by editing using CRISPR/Cas9 ribonucleoproteins and characterization of the modified single-cell clones.

RNA Editing

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2020

RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...

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