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利用高效 TALEN 系统进行体内基因组编辑。

In vivo genome editing using a high-efficiency TALEN system.

机构信息

Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

Nature. 2012 Nov 1;491(7422):114-8. doi: 10.1038/nature11537. Epub 2012 Sep 23.

DOI:10.1038/nature11537
PMID:23000899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3491146/
Abstract

The zebrafish (Danio rerio) is increasingly being used to study basic vertebrate biology and human disease with a rich array of in vivo genetic and molecular tools. However, the inability to readily modify the genome in a targeted fashion has been a bottleneck in the field. Here we show that improvements in artificial transcription activator-like effector nucleases (TALENs) provide a powerful new approach for targeted zebrafish genome editing and functional genomic applications. Using the GoldyTALEN modified scaffold and zebrafish delivery system, we show that this enhanced TALEN toolkit has a high efficiency in inducing locus-specific DNA breaks in somatic and germline tissues. At some loci, this efficacy approaches 100%, including biallelic conversion in somatic tissues that mimics phenotypes seen using morpholino-based targeted gene knockdowns. With this updated TALEN system, we successfully used single-stranded DNA oligonucleotides to precisely modify sequences at predefined locations in the zebrafish genome through homology-directed repair, including the introduction of a custom-designed EcoRV site and a modified loxP (mloxP) sequence into somatic tissue in vivo. We further show successful germline transmission of both EcoRV and mloxP engineered chromosomes. This combined approach offers the potential to model genetic variation as well as to generate targeted conditional alleles.

摘要

斑马鱼(Danio rerio)越来越多地被用于研究基本的脊椎动物生物学和人类疾病,具有丰富的体内遗传和分子工具。然而,无法以靶向方式轻易地修饰基因组一直是该领域的一个瓶颈。在这里,我们展示了改进的人工转录激活因子样效应物核酸酶(TALEN)为靶向斑马鱼基因组编辑和功能基因组应用提供了一种强大的新方法。使用改良的 GoldyTALEN 支架和斑马鱼传递系统,我们表明这种增强的 TALEN 工具包在诱导体细胞核和生殖组织中的特定基因座的 DNA 断裂方面具有很高的效率。在某些基因座上,这种效率接近 100%,包括模拟基于 morpholino 的靶向基因敲低所观察到的表型的体细胞中双等位基因转换。使用此更新的 TALEN 系统,我们成功地使用单链 DNA 寡核苷酸通过同源定向修复精确修饰斑马鱼基因组中预设位置的序列,包括在体内将自定义设计的 EcoRV 位点和改良的 loxP (mloxP) 序列引入体细胞组织。我们进一步展示了 EcoRV 和 mloxP 工程染色体在生殖系中的成功传递。这种组合方法具有模拟遗传变异以及产生靶向条件等位基因的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/f4ff325d41c7/nihms405887f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/0dbe5a8529d9/nihms405887f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/7e658bb322f8/nihms405887f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/9101718cfc16/nihms405887f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/051c56685271/nihms405887f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/f4ff325d41c7/nihms405887f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/0dbe5a8529d9/nihms405887f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/7e658bb322f8/nihms405887f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/9101718cfc16/nihms405887f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/051c56685271/nihms405887f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a566/3491146/f4ff325d41c7/nihms405887f5.jpg

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Nucleic Acids Res. 2012 Sep;40(16):8001-10. doi: 10.1093/nar/gks518. Epub 2012 Jun 7.
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Aligning with the 3Rs: alternative models for research into muscle development and inherited myopathies.与 3Rs 保持一致:肌肉发育和遗传性肌肉疾病研究的替代模型。
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