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.
Large-Scale Transgenic Drosophila Resource Collections for Loss- and Gain-of-Function Studies.
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作者:Zirin Jonathan, Hu Yanhui, Liu Luping, Yang-Zhou Donghui, Colbeth Ryan, Yan Dong, Ewen-Campen Ben, Tao Rong, Vogt Eric, VanNest Sara, Cavers Cooper, Villalta Christians, Comjean Aram, Sun Jin, Wang Xia, Jia Yu, Zhu Ruibao, Peng Ping, Yu Jinchao, Shen Da, Qiu Yuhao, Ayisi Limmond, Ragoowansi Henna, Fenton Ethan, Efrem Senait, Parks Annette, Saito Kuniaki, Kondo Shu, Perkins Liz, Mohr Stephanie E, Ni Jianquan, Perrimon Norbert
| 期刊: | Genetics | 影响因子: | 5.100 |
| 时间: | 2020 | 起止号: | 2020 Apr;214(4):755-767 |
| doi: | 10.1534/genetics.119.302964 | ||
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