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Modulating CRISPR gene drive activity through nucleocytoplasmic localization of Cas9 in .

Fungal Biol Biotechnol. 2019-01; 
GoeckelMegan E,BasgallErianna M,LewisIsabel C,GoettingSamantha C,YanYao,HalloranMegan,FinniganGrego
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Codon Optimization Second, custom genes were synthesized (GenScript, Piscataway, NJ) containing the 3′ most 180 bp of eGFP, a C-terminal NLS or NES signal, stop codon, and 191 bps of the 3′ UTR of CDC10. Get A Quote

摘要

The bacterial CRISPR/Cas genome editing system has provided a major breakthrough in molecular biology. One use of this technology is within a nuclease-based gene drive. This type of system can install a genetic element within a population at unnatural rates. Combatting of vector-borne diseases carried by metazoans could benefit from a delivery system that bypasses traditional Mendelian laws of segregation. Recently, laboratory studies in fungi, insects, and even mice, have demonstrated successful propagation of CRISPR gene drives and the potential utility of this type of mechanism. However, current gene drives still face challenges including evolved resistance, containment, and the consequences of... More

關鍵詞

Biotechnology,CRISPR,Cas9,Gene drive,Nucleocytoplasmic trafficking,Y
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