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CRISPR-based modular assembly of a UAS-cDNA/ORF plasmid library for more than 5500 Drosophila genes conserved in humans

Genome Res. 2020-01; 
Wei P, Xue W,, Zhao Y, Ning G, Wang J,.
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GenCrispr Cas9 Genome Editing To evaluate sgRNAs targeting vector backbone sequences that are adjacent to the 5′ end of cDNAs or ORFs in cDNA/ORF plasmids, we performed in vitro CRISPR/Cas9 cleavage analysis of DNA substrates. A 5-μL CRISPR/Cas9 cleavage reaction contains 0.2 μL 1.22 μM S. pyogenes Cas9 (GenScript Z03386-50), 0.5 μL 20 ng/μL sgRNA, 0.015 pmol DNA substrate, 0.5 μL 10× Cas9 Buffer, and DEPC-treated water.  Get A Quote

摘要

Construction of a genome-wide transgenic UAS-cDNA/ORF library in Drosophila based on the binary GAL4/UAS system has been severely hampered by technical difficulties, although genome-wide cDNA or ORF resources of Drosophila, human, and mouse have been publicly available for more than a decade. Here, we developed a new method named CRISPR-based modular assembly (CRISPRmass) for the high-throughput construction of a genome-wide UAS-cDNA/ORF library from publicly available cDNA/ORF resources. Through cleavage of shared vector sequences of cDNA/ORF plasmids by CRISPR/Cas9 and subsequent insertion of UAS modules by Gibson assembly, the procedure of construction of such a library by CRISPRmass is standardized as massi... More

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