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Structural Elements of DNA and RNA Eukaryotic Expression Vectors for In Vitro and In Vivo Genome Editor Delivery
A A Zagoskin1, M V Zakharova1, M O Nagornykh1,2
1Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, 142290 Pushchino, Russia.
Molecular Biology
|December 19, 2022
Summary
Gene editing technologies offer new possibilities in medicine and agriculture. This review focuses on nonviral methods for delivering gene editing tools, crucial for safe and effective therapeutic applications.
Area of Science:
- Biotechnology
- Molecular Biology
- Genetics
Background:
- Gene editing technologies, utilizing programmable nucleases, are advancing fields like healthcare and agriculture.
- A significant hurdle for therapeutic gene editing is the efficient and safe delivery of editors into target cells and tissues.
- Both viral and nonviral systems are established methods for delivering gene editing components.
Purpose of the Study:
- To review the structural characteristics of nonviral expression vectors for gene editing.
- To explore various delivery methodologies for these nonviral vectors.
- To cover in vitro and in vivo applications of nonviral gene editing delivery systems.
Main Methods:
- Literature review of nonviral DNA and RNA-based expression vectors.
- Analysis of gene editor delivery techniques.
- Examination of in vitro and in vivo experimental approaches.
Main Results:
- Nonviral vectors offer diverse structural designs for gene editing applications.
- Various delivery strategies exist for nonviral gene editing systems.
- Successful in vitro and in vivo delivery methods have been identified.
Conclusions:
- Nonviral vectors are a viable alternative for gene editor delivery.
- Understanding vector design and delivery methods is key to therapeutic success.
- Further research into nonviral systems will enhance gene editing applications.
Keywords:
Cas9GENE THERAPYIVT RNANANOPARTICLESTALENZFNexpression DNA vectorgenome editingmRNA-based deliveryMore Related Videos
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