Exosome/Liposome-like Nanoparticles: New Carriers for CRISPR Genome Editing in Plants

被引:39
作者
Alghuthaymi, Mousa A. [1 ]
Ahmad, Aftab [2 ,3 ]
Khan, Zulqurnain [4 ]
Khan, Sultan Habibullah [3 ]
Ahmed, Farah K. [5 ]
Faiz, Sajid [6 ]
Nepovimova, Eugenie [7 ]
Kuca, Kamil [7 ]
Abd-Elsalam, Kamel A. [8 ]
机构
[1] Shaqra Univ, Sci & Humanities Coll, Biol Dept, Alquwayiyah 19245, Saudi Arabia
[2] Univ Agr Faisalabad, Dept Biochem, Faisalabad 38040, Pakistan
[3] Univ Agr Faisalabad, Ctr Adv Studies Agr & Food Secur CASAFS, Faisalabad 38040, Pakistan
[4] MNS Univ Agr, Inst Plant Breeding & Biotechnol, Multan 60000, Pakistan
[5] Cairo Univ, Fac Agr, Biotechnol English Program, Giza 12613, Egypt
[6] Univ Haripur, Dept Plant Breeding & Genet, Haripur 22620, Pakistan
[7] Univ Hradec Kralove, Fac Sci, Dept Chem, Hradec Kralove 50003, Czech Republic
[8] Agr Res Ctr ARC, Plant Pathol Res Inst, 9 Gamaa St, Giza 12619, Egypt
关键词
genome editing; CRISPR; nanoparticles; exosomes and liposomes; SOLID-LIPID NANOPARTICLES; GENE DELIVERY; CAS9; RIBONUCLEOPROTEIN; TARGETED MUTAGENESIS; EFFICIENT DELIVERY; HIGHLY EFFICIENT; DRUG-DELIVERY; MAGNETIC NANOPARTICLES; MEDIATED DELIVERY; SYSTEM COMPONENTS;
D O I
10.3390/ijms22147456
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rapid developments in the field of plant genome editing using clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein (Cas) systems necessitate more detailed consideration of the delivery of the CRISPR system into plants. Successful and safe editing of plant genomes is partly based on efficient delivery of the CRISPR system. Along with the use of plasmids and viral vectors as cargo material for genome editing, non-viral vectors have also been considered for delivery purposes. These non-viral vectors can be made of a variety of materials, including inorganic nanoparticles, carbon nanotubes, liposomes, and protein- and peptide-based nanoparticles, as well as nanoscale polymeric materials. They have a decreased immune response, an advantage over viral vectors, and offer additional flexibility in their design, allowing them to be functionalized and targeted to specific sites in a biological system with low cytotoxicity. This review is dedicated to describing the delivery methods of CRISPR system into plants with emphasis on the use of non-viral vectors.
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页数:22
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