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Genome Editing in Mammalian Cell Lines using CRISPR-Cas
Published on: April 11, 2019
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Gene editing for cell engineering: trends and applications.
Sanjeev K Gupta1,2, Pratyoosh Shukla1
1a Department of Microbiology, Enzyme Technology and Protein Bioinformatics Laboratory , Maharshi Dayanand University , Rohtak , Haryana , India.
Critical Reviews in Biotechnology
|August 19, 2016
Summary
Modern gene editing tools like CRISPR-Cas9 enable efficient manipulation of yeast and mammalian cells for producing therapeutic proteins. Multiplexed gene editing accelerates product development, improving yield, quality, and affordability.
Area of Science:
- Molecular Biology
- Biotechnology
- Genetic Engineering
Background:
- Gene editing tools like CRISPR, TALENs, and ZFNs facilitate host genome manipulation.
- Industrial production hosts such as yeast and mammalian cells can be modified for cost-effective recombinant protein development.
Purpose of the Study:
- To review modern gene editing tools for host genome modification.
- To emphasize CRISPR-Cas9's multiplexing capabilities for yeast and CHO cell genetic manipulation.
Main Methods:
- Review of CRISPR, TALENs, and ZFNs gene editing technologies.
- Focus on multiplexed gene editing strategies for knock-in/knock-out events.
Main Results:
- Multiplexed gene editing revolutionizes knock-out and knock-in events in yeast and CHO cells.
- Enables high, stable, and consistent transgene expression for therapeutic proteins like monoclonal antibodies.
Conclusions:
- CRISPR-Cas9 facilitates rapid genetic manipulation of production hosts.
- Leads to faster product development with improved yield, quality, and affordability.
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