| Literature DB >> 32071193 |
Jonathan Zirin1, Yanhui Hu2, Luping Liu2, Donghui Yang-Zhou2, Ryan Colbeth2, Dong Yan3, Ben Ewen-Campen2, Rong Tao2, Eric Vogt2, Sara VanNest2, Cooper Cavers2, Christians Villalta2, Aram Comjean2, Jin Sun4, Xia Wang4, Yu Jia4, Ruibao Zhu4, Ping Peng4, Jinchao Yu4, Da Shen4, Yuhao Qiu4, Limmond Ayisi2, Henna Ragoowansi2, Ethan Fenton2, Senait Efrem2, Annette Parks5, Kuniaki Saito6, Shu Kondo6, Liz Perkins2, Stephanie E Mohr2, Jianquan Ni7, Norbert Perrimon1,8.
Abstract
The Transgenic RNAi Project (TRiP), a Drosophila melanogaster functional genomics platform at Harvard Medical School, was initiated in 2008 to generate and distribute a genome-scale collection of RNA interference (RNAi) fly stocks. To date, it has generated >15,000 RNAi fly stocks. As this covers most Drosophila genes, we have largely transitioned to development of new resources based on CRISPR technology. Here, we present an update on our libraries of publicly available RNAi and CRISPR fly stocks, and focus on the TRiP-CRISPR overexpression (TRiP-OE) and TRiP-CRISPR knockout (TRiP-KO) collections. TRiP-OE stocks express single guide RNAs targeting upstream of a gene transcription start site. Gene activation is triggered by coexpression of catalytically dead Cas9 fused to an activator domain, either VP64-p65-Rta or Synergistic Activation Mediator. TRiP-KO stocks express one or two single guide RNAs targeting the coding sequence of a gene or genes. Cutting is triggered by coexpression of Cas9, allowing for generation of indels in both germline and somatic tissue. To date, we have generated >5000 TRiP-OE or TRiP-KO stocks for the community. These resources provide versatile, transformative tools for gene activation, gene repression, and genome engineering.Entities:
Keywords: CRISPR; Cas9; Drosophila; RNAi; knockout; overexpression; phenotypes; screens
Mesh:
Year: 2020 PMID: 32071193 PMCID: PMC7153935 DOI: 10.1534/genetics.119.302964
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562