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Updated: Nov 1, 2025

Genome Editing in Mammalian Cell Lines using CRISPR-Cas
Published on: April 11, 2019
Recent advances in CRISPR technologies for genome editing
Myeonghoon Song1, Taeyoung Koo2,3,4
1Department of life and Nanopharmaceutical Sciences, College of Pharmacy, Kyung Hee University, Seoul, Republic of Korea.
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) system revolutionized genome editing, enabling precise genetic manipulation across diverse organisms. Ongoing advancements aim to enhance CRISPR/Cas tools and address current limitations for broader applications.
Area of Science:
- Molecular Biology
- Genetics
- Biotechnology
Background:
- The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) system has emerged as a transformative technology in genome editing.
- CRISPR/Cas-based precise genome editing is now a widely adopted platform in various organisms, from plants to animals.
Purpose of the Study:
- To review recent advancements in CRISPR/Cas-based genome editing tools.
- To discuss the ongoing development and modifications of the CRISPR/Cas system for enhanced efficiency and fidelity.
- To highlight limitations and concerns associated with current CRISPR/Cas technologies.
Main Methods:
- Review of recent scientific literature on CRISPR/Cas tools.
- Analysis of modifications to Cas effector proteins for diverse genetic manipulations.
- Examination of strategies to overcome limitations in CRISPR/Cas applications.
Main Results:
- CRISPR/Cas systems have been extensively modified, enabling precise genome editing, base editing, transposition, recombination, and epigenetic regulation.
- Continuous development is addressing challenges such as off-target effects, limited targeting scope, and delivery issues.
- A diverse array of CRISPR/Cas-based tools are available for genetic manipulation.
Conclusions:
- CRISPR/Cas technology has revolutionized genome editing with broad applicability.
- Ongoing research focuses on improving CRISPR/Cas tools' efficiency, specificity, and delivery for therapeutic and engineering purposes.
- Understanding limitations and concerns is crucial for responsible development and application of CRISPR/Cas technologies.
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