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* These authors contributed equally
We present a protocol for CRISPR-based modular assembly (CRISPRmass), a method for high-throughput construction of UAS-cDNA/ORF plasmid library in Drosophila using publicly available cDNA/ORF resources. CRISPRmass can be applied to editing various plasmid libraries.
Functional genomics screening offers a powerful approach to probe gene function and relies on the construction of genome-wide plasmid libraries. Conventional approaches for plasmid library construction are time-consuming and laborious. Therefore, we recently developed a simple and efficient method, CRISPR-based modular assembly (CRISPRmass), for high-throughput construction of a genome-wide upstream activating sequence-complementary DNA/open reading frame (UAS-cDNA/ORF) plasmid library. Here, we present a protocol for CRISPRmass, taking as an example the construction of a GAL4/UAS-based UAS-cDNA/ORF plasmid library. The protocol includes massively parallel two-step test tube reactions followed by bacterial transformation. The first step is to linearize the existing complementary DNA (cDNA) or open reading frame (ORF) cDNA or ORF library plasmids by cutting the shared upstream vector sequences adjacent to the 5' end of cDNAs or ORFs using CRISPR/Cas9 together with single guide RNA (sgRNA), and the second step is to insert a UAS module into the linearized cDNA or ORF plasmids using a single step reaction. CRISPRmass allows the simple, fast, efficient, and cost-effective construction of various plasmid libraries. The UAS-cDNA/ORF plasmid library can be utilized for gain-of-function screening in cultured cells and for constructing a genome-wide transgenic UAS-cDNA/ORF library in Drosophila.
Unbiased whole-genome genetic screening is a powerful approach for identifying genes involved in a given biological process and elucidating its mechanism. Therefore, it is widely used in various fields of biological research. Approximately 60% of Drosophila genes are conserved in humans1,2, and ~75% of human disease genes have homologs in Drosophila3. Genetic screening is mainly divided into two types: loss of function (LOF) and gain of function (GOF). LOF genetic screens in Drosophila have played a critical role in elucidating mechanisms that govern nearly ev....
1. Determination of optimal Cas9/sgRNA cleavage site upstream of cDNA/ORF
We applied CRISPRmass to generate a genome-wide UAS-cDNA/ORF plasmid library using 3402 cDNA/ORF clones bearing pOT2 vector backbone from the DGRC Gold Collection. We randomly analyzed only one colony for each UAS-cDNA/ORF construct, and subsequent restriction analysis with PstI indicated that 98.6% of UAS-cDNA/ORF constructs were created successfully9. The rationale for using PstI for restriction analysis of UAS-cDNA/ORF constructs bearing pOT2 vector backbone is as follows. There are two PstI si.......
The most critical steps of CRISPRmass are the design of sgRNAs and the evaluation of sgRNAs. Selection of highly efficient sgRNAs for Cas9 is key to the success of CRISPRmass. If very few or no colonies are observed on the majority of antibiotic-containing LB plates after the transformation of E. coli with single-step reaction assembly products, check plasmid digestion by agarose gel electrophoresis. If plasmids are not well digested, check Cas9 activity, sgRNA degradation and plasmid quality; if plasmids are well digest.......
This work was sponsored by the National Natural Science Foundation of China (32071135 and 31471010), the Shanghai Pujiang Program (14PJ1405900), and the Natural Science Foundation of Shanghai (19ZR1446400).
....Name | Company | Catalog Number | Comments |
Aluminum Cooling Block | Aikbbio | ADMK-0296 | To perform bacterial transformation |
DEPC-Treated Water | Invitrogen | AM9906 | |
Gel Extraction Kit | Omega | D2500 | To purify DNA from agarose gel |
Gel Imaging System | Tanon | 2500B | |
HiScribe T7 Quick High Yield RNA Synthesis Kit | NEB | E2050 | |
NEBuilder HiFi DNA Assembly Master Mix | NEB | E2621 | |
Plasmid Mini Kit | Omega | D6943 | To isolate plasmid DNA from bacterial cells |
Q5 Hot Start High-Fidelity 2x Master Mix | NEB | M0494 | |
S. pyogenes Cas9 | GenScript | Z03386 | |
Shaking Incubator | Shanghai Zhichu | ZQLY-180V | |
T series Multi-Block Thermal Cycler | LongGene | T20 | To perform PCR |
Trans10 Chemically Competent Cell | TranGen BioTech | CD101 | |
Ultraviolet spectrophotometer | Shimadzu | BioSpec-nano | To measure concentration of DNA or RNA |
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