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Zinc-finger nucleases: new strategies to target the rat genome.锌指核酸酶:靶向大鼠基因组的新策略。
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2
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3
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本文引用的文献

1
Direct reprogramming of rat neural precursor cells and fibroblasts into pluripotent stem cells.将大鼠神经前体细胞和纤维母细胞直接重编程为多能干细胞。
PLoS One. 2010 Mar 24;5(3):e9838. doi: 10.1371/journal.pone.0009838.
2
Generation of knockout rats with X-linked severe combined immunodeficiency (X-SCID) using zinc-finger nucleases.利用锌指核酸酶生成 X 连锁重症联合免疫缺陷(X-SCID)敲除大鼠。
PLoS One. 2010 Jan 25;5(1):e8870. doi: 10.1371/journal.pone.0008870.
3
Genome editing with modularly assembled zinc-finger nucleases.使用模块化组装锌指核酸酶进行基因组编辑。
Nat Methods. 2010 Feb;7(2):91; author reply 91-2. doi: 10.1038/nmeth0210-91a.
4
Generation of a triple-gene knockout mammalian cell line using engineered zinc-finger nucleases.利用基因工程锌指核酸酶生成三基因敲除哺乳动物细胞系。
Biotechnol Bioeng. 2010 May 1;106(1):97-105. doi: 10.1002/bit.22654.
5
Generation of gene-specific mutated rats using zinc-finger nucleases.利用锌指核酸酶生成基因特异性突变大鼠。
Methods Mol Biol. 2010;597:211-25. doi: 10.1007/978-1-60327-389-3_15.
6
The rat genome database curators: who, what, where, why.大鼠基因组数据库管理者:何人、何事、何地、为何。
PLoS Comput Biol. 2009 Nov;5(11):e1000582. doi: 10.1371/journal.pcbi.1000582. Epub 2009 Nov 26.
7
BAK and BAX deletion using zinc-finger nucleases yields apoptosis-resistant CHO cells.使用锌指核酸酶进行 BAK 和 BAX 缺失可产生抗凋亡的 CHO 细胞。
Biotechnol Bioeng. 2010 Feb 1;105(2):330-40. doi: 10.1002/bit.22541.
8
Efficient targeting of expressed and silent genes in human ESCs and iPSCs using zinc-finger nucleases.利用锌指核酸酶有效靶向人类胚胎干细胞和诱导多能干细胞中的表达基因和沉默基因。
Nat Biotechnol. 2009 Sep;27(9):851-7. doi: 10.1038/nbt.1562. Epub 2009 Aug 13.
9
Targeted manipulation of mammalian genomes using designed zinc finger nucleases.利用设计的锌指核酸酶对哺乳动物基因组进行靶向操作。
Biochem Biophys Res Commun. 2009 Oct 9;388(1):56-61. doi: 10.1016/j.bbrc.2009.07.112. Epub 2009 Jul 25.
10
Knockout rats via embryo microinjection of zinc-finger nucleases.通过胚胎显微注射锌指核酸酶制备基因敲除大鼠。
Science. 2009 Jul 24;325(5939):433. doi: 10.1126/science.1172447.

锌指核酸酶:靶向大鼠基因组的新策略。

Zinc-finger nucleases: new strategies to target the rat genome.

机构信息

Cardiovascular Research Center, Medical College of Wisconsin, Milwaukee, 53226, USA.

出版信息

Clin Sci (Lond). 2010 Jul 6;119(8):303-11. doi: 10.1042/CS20100201.

DOI:10.1042/CS20100201
PMID:20615201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3549593/
Abstract

The importance of genetic laboratory models, such as mice and rats, becomes evident when there is a poor understanding of the nature of human disease. Many rat models for human disease, created over the years by phenotype-driven strategies, now provide a foundation for the identification of their genetic determinants. These models are especially valuable with the emerging need for validation of genes found in genome-wide association studies for complex diseases. The manipulation of the rat genome using engineered zinc-finger nucleases now introduces a key technology for manipulating the rat genome, which is broadly applicable. The ability to generate knockout rat models using zinc-finger nuclease technology will now enable its full emergence as an exceptional physiological and genetic research model.

摘要

当人们对人类疾病的本质缺乏了解时,遗传实验室模型(如老鼠)的重要性就变得显而易见了。多年来,许多用于人类疾病的大鼠模型都是通过表型驱动策略创建的,现在为鉴定其遗传决定因素提供了基础。随着对全基因组关联研究中发现的复杂疾病相关基因进行验证的需求不断增加,这些模型尤其具有价值。利用工程化锌指核酸酶对大鼠基因组进行操作,为大鼠基因组的操作引入了一项关键技术,具有广泛的适用性。利用锌指核酸酶技术生成基因敲除大鼠模型的能力,将使其作为一种出色的生理和遗传研究模型而全面崛起。