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本文引用的文献

1
Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases.利用工程化锌指核酸酶在斑马鱼中进行靶向基因失活。
Nat Biotechnol. 2008 Jun;26(6):695-701. doi: 10.1038/nbt1398. Epub 2008 May 25.
2
Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleases.利用设计的锌指核酸酶在斑马鱼中进行可遗传的靶向基因破坏。
Nat Biotechnol. 2008 Jun;26(6):702-8. doi: 10.1038/nbt1409. Epub 2008 May 25.
3
Standardized reagents and protocols for engineering zinc finger nucleases by modular assembly.通过模块化组装构建锌指核酸酶的标准化试剂和方案。
Nat Protoc. 2006;1(3):1637-52. doi: 10.1038/nprot.2006.259.
4
Gene targeting using zinc finger nucleases.使用锌指核酸酶进行基因靶向。
Nat Biotechnol. 2005 Aug;23(8):967-73. doi: 10.1038/nbt1125.

用于斑马鱼基因的锌指基因敲除技术

Zinc finger-based knockout punches for zebrafish genes.

作者信息

Ekker Stephen C

机构信息

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

出版信息

Zebrafish. 2008 Summer;5(2):121-3. doi: 10.1089/zeb.2008.9988.

DOI:10.1089/zeb.2008.9988
PMID:18554175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2849655/
Abstract

The ability to manipulate the genome is critical to develop and test hypotheses based on genetics. Knockdown strategies focused on RNAi and/or morpholinos are excellent genetic tools, but they come with substantial technical limitations. A new gene targeting approach employing synthetic zinc finger nuclease (ZFN) technology is a powerful and complementary approach to directly modify genetic loci for many diverse applications, notably enhancing Danio rerio (the zebrafish) as an experimental organism for understanding human disease. This ZFN-based technology to generate targeted knockouts in this aquatic animal opens the door to an array of new biological models of human disease and genetic testing.

摘要

操纵基因组的能力对于基于遗传学提出和检验假设至关重要。专注于RNA干扰和/或吗啉代的敲低策略是出色的遗传学工具,但它们存在重大技术限制。一种采用合成锌指核酸酶(ZFN)技术的新型基因靶向方法是一种强大的补充方法,可直接修饰基因座以用于多种不同应用,特别是增强斑马鱼作为理解人类疾病的实验生物的作用。这种基于ZFN技术在这种水生动物中产生靶向敲除的方法为一系列人类疾病新生物模型和基因检测打开了大门。