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10.1038/s41467-018-05262-w

http://scihub22266oqcxt.onion/10.1038/s41467-018-05262-w
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C6057936!6057936!30042426
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suck abstract from ncbi


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pmid30042426      Nat+Commun 2018 ; 9 (ä): ä
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  • Introduction of pathogenic mutations into the mouse Psen1 gene by Base Editor and Target-AID #MMPMID30042426
  • Sasaguri H; Nagata K; Sekiguchi M; Fujioka R; Matsuba Y; Hashimoto S; Sato K; Kurup D; Yokota T; Saido TC
  • Nat Commun 2018[]; 9 (ä): ä PMID30042426show ga
  • Base Editor (BE) and Target-AID (activation-induced cytidine deaminase) are engineered genome-editing proteins composed of Cas9 and cytidine deaminases. These base-editing tools convert C:G base pairs to T:A at target sites. Here, we inject either BE or Target-AID mRNA together with identical single-guide RNAs (sgRNAs) into mouse zygotes, and compare the base-editing efficiencies of the two distinct tools in vivo. BE consistently show higher base-editing efficiency (10.0?62.8%) compared to that of Target-AID (3.4?29.8%). However, unexpected base substitutions and insertion/deletion formations are also more frequently observed in BE-injected mice or zygotes. We are able to generate multiple mouse lines harboring point mutations in the mouse presenilin 1 (Psen1) gene by injection of BE or Target-AID. These results demonstrate that BE and Target-AID are highly useful tools to generate mice harboring pathogenic point mutations and to analyze the functional consequences of the mutations in vivo.
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