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本文引用的文献

1
A large-scale resource for tissue-specific CRISPR mutagenesis in .大规模组织特异性 CRISPR 基因敲除资源库。
Elife. 2020 Feb 13;9:e53865. doi: 10.7554/eLife.53865.
2
Spz/Toll-6 signal guides organotropic metastasis in .Spz/Toll-6 信号指导器官趋向性转移。
Dis Model Mech. 2019 Oct 7;12(10):dmm039727. doi: 10.1242/dmm.039727.
3
Intellectual disability and autism spectrum disorders 'on the fly': insights from .智力残疾和自闭症谱系障碍“随机应变”:. 的见解
Dis Model Mech. 2019 May 13;12(5):dmm039180. doi: 10.1242/dmm.039180.
4
Tissue-specific (ts)CRISPR as an efficient strategy for in vivo screening in Drosophila.组织特异性 (ts)CRISPR 作为一种在果蝇体内进行筛选的有效策略。
Nat Commun. 2019 May 8;10(1):2113. doi: 10.1038/s41467-019-10140-0.
5
OMIM.org: leveraging knowledge across phenotype-gene relationships.OMIM.org:利用表型-基因关系中的知识。
Nucleic Acids Res. 2019 Jan 8;47(D1):D1038-D1043. doi: 10.1093/nar/gky1151.
6
FlyBase 2.0: the next generation.FlyBase 2.0:下一代。
Nucleic Acids Res. 2019 Jan 8;47(D1):D759-D765. doi: 10.1093/nar/gky1003.
7
Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease.遗传诊断对先前未确诊疾病患者的影响。
N Engl J Med. 2018 Nov 29;379(22):2131-2139. doi: 10.1056/NEJMoa1714458. Epub 2018 Oct 10.
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A Druggable Genome Screen Identifies Modifiers of α-Synuclein Levels via a Tiered Cross-Species Validation Approach.药物基因组筛选通过分层跨物种验证方法鉴定α-突触核蛋白水平的调节剂。
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大规模转基因资源库用于功能丧失和获得研究。

Large-Scale Transgenic Resource Collections for Loss- and Gain-of-Function Studies.

机构信息

Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, Massachusetts 02115

Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Genetics. 2020 Apr;214(4):755-767. doi: 10.1534/genetics.119.302964. Epub 2020 Feb 18.

DOI:10.1534/genetics.119.302964
PMID:32071193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7153935/
Abstract

The Transgenic RNAi Project (TRiP), a 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 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.

摘要

转基因 RNAi 项目(TRiP)是哈佛医学院的一个功能基因组学平台,于 2008 年启动,旨在生成和分发大规模的 RNA 干扰(RNAi)果蝇品系库。迄今为止,它已经生成了超过 15000 种 RNAi 果蝇品系。由于这涵盖了大多数基因,我们已经在很大程度上转向基于 CRISPR 技术的新资源的开发。在这里,我们介绍了我们公开可用的 RNAi 和 CRISPR 果蝇品系库的最新情况,并重点介绍了 TRiP-CRISPR 过表达(TRiP-OE)和 TRiP-CRISPR 敲除(TRiP-KO)库。TRiP-OE 品系表达靶向基因转录起始位点上游的单个向导 RNA。通过共表达与激活结构域融合的无催化活性 Cas9(VP64-p65-Rta 或协同激活介体)来触发基因激活。TRiP-KO 品系表达靶向一个或两个基因编码序列的一个或两个向导 RNA。通过共表达 Cas9 触发切割,允许在生殖系和体细胞组织中产生插入缺失。迄今为止,我们已经为社区生成了超过 5000 种 TRiP-OE 或 TRiP-KO 品系。这些资源为基因激活、基因沉默和基因组工程提供了多功能、变革性的工具。