How does Base Editing work?
- ScienceWise
- Apr 23
- 1 min read
Updated: Apr 24
Base editing is a form of gene editing that precisely alters single DNA bases, like changing "A" to "G" or "C" to "T", without creating breaks in the DNA. It uses a modified CRISPR-Cas9 system where a CRISPR-associated protein (Cas) is fused to a base-modifying enzyme, allowing for targeted chemical modifications of DNA bases.
Here's a more detailed explanation:
How it works:
1. Targeting:
A guide RNA molecule, similar to CRISPR-Cas9, directs the base editing complex to a specific DNA sequence.
2. Base modification:
The base-modifying enzyme, a deaminase, chemically converts one DNA base into another.
3. Repair:
Cellular repair mechanisms then take over, ensuring the modified base is correctly incorporated into the DNA.
Key features:
Precise:
Base editing allows for precise changes at the single-base level.
No DSBs:
Unlike traditional CRISPR-Cas9, base editing does not create double-strand breaks (DSBs), which can lead to unintended edits.
Versatile:
Base editors can be engineered to target different base pairs, enabling a range of edits.
Therapeutic potential:
Base editing holds promise for treating genetic diseases caused by single-base mutations.

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