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Enhanced Efficiency of flySAM by Optimization of sgRNA Parameters in Drosophila.


ABSTRACT: The flySAM/CRISPRa system has recently emerged as a powerful tool for gain-of-function studies in Drosophila melanogaster This system includes Gal4/UAS-driven dCas9 activators and U6 promoter-controlled sgRNA. Having established dCas9 activators superior to other combinations, to further enhance the efficiency of the targeting activators we systematically optimized the parameters of the sgRNA. Interestingly, the most efficient sgRNAs were found to accumulate in the region from -150bp to -450bp upstream of the transcription start site (TSS), and the activation efficiency showed a strong positive correlation with the GC content of the sgRNA targeting sequence. In addition, the target region is dominant to the GC content, as sgRNAs targeting areas beyond -600bp from the TSS lose efficiency even when containing 75% GC. Surprisingly, when comparing the activities of sgRNAs targeting to either DNA strand, sgRNAs targeting to the non-template strand outperform those complementary to the template strand, both in cells and in vivo In summary, we define criteria for sgRNA design which will greatly facilitate the application of CRISPRa in gain-of-function studies.

SUBMITTER: Mao D 

PROVIDER: S-EPMC7718753 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Enhanced Efficiency of flySAM by Optimization of sgRNA Parameters in <i>Drosophila</i>.

Mao Decai D   Jia Yu Y   Peng Ping P   Shen Da D   Ren Xingjie X   Zhu Ruibao R   Qiu Yuhao Y   Han Yuting Y   Yu Jinchao J   Che Qinyun Q   Li Yutong Y   Lu Xinyi X   Liu Lu-Ping LP   Wang Zhao Z   Liu Qingfei Q   Sun Jin J   Ni Jian-Quan JQ  

G3 (Bethesda, Md.) 20201203 12


The flySAM/CRISPRa system has recently emerged as a powerful tool for gain-of-function studies in <i>Drosophila melanogaster</i> This system includes Gal4/UAS-driven dCas9 activators and U6 promoter-controlled sgRNA. Having established dCas9 activators superior to other combinations, to further enhance the efficiency of the targeting activators we systematically optimized the parameters of the sgRNA. Interestingly, the most efficient sgRNAs were found to accumulate in the region from -150bp to -  ...[more]

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