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本文引用的文献

1
Production of p53 gene knockout rats by homologous recombination in embryonic stem cells.利用胚胎干细胞中的同源重组生产 p53 基因敲除大鼠。
Nature. 2010 Sep 9;467(7312):211-3. doi: 10.1038/nature09368. Epub 2010 Aug 11.
2
Generation of genetically modified rats from embryonic stem cells.从胚胎干细胞生成基因修饰大鼠。
Proc Natl Acad Sci U S A. 2010 Aug 10;107(32):14223-8. doi: 10.1073/pnas.1009582107. Epub 2010 Jul 26.
3
Targeted genome modification in mice using zinc-finger nucleases.利用锌指核酸酶对小鼠进行靶向基因组修饰。
Genetics. 2010 Oct;186(2):451-9. doi: 10.1534/genetics.110.117002. Epub 2010 Jul 13.
4
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。
Clin Sci (Lond). 2010 Jul 6;119(8):303-11. doi: 10.1042/CS20100201.
5
Zinc-finger nuclease-driven targeted integration into mammalian genomes using donors with limited chromosomal homology.锌指核酸酶驱动的靶向整合到哺乳动物基因组中,使用有限同源染色体的供体。
Nucleic Acids Res. 2010 Aug;38(15):e152. doi: 10.1093/nar/gkq512. Epub 2010 Jun 8.
6
Functional genomics, proteomics, and regulatory DNA analysis in isogenic settings using zinc finger nuclease-driven transgenesis into a safe harbor locus in the human genome.在同源环境中使用锌指核酸酶驱动的转基因技术进行功能基因组学、蛋白质组学和调控 DNA 分析,将其转入人类基因组中的安全港位点。
Genome Res. 2010 Aug;20(8):1133-42. doi: 10.1101/gr.106773.110. Epub 2010 May 27.
7
Generating knockout rats by transposon mutagenesis in spermatogonial stem cells.利用精原干细胞中的转座子突变生成基因敲除大鼠。
Nat Methods. 2010 Jun;7(6):443-5. doi: 10.1038/nmeth.1461. Epub 2010 May 16.
8
The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance.自发性高血压大鼠的基因组序列:分析与功能意义。
Genome Res. 2010 Jun;20(6):791-803. doi: 10.1101/gr.103499.109. Epub 2010 Apr 29.
9
Efficient mammalian germline transgenesis by cis-enhanced Sleeping Beauty transposition.通过顺式增强的睡美人转座实现高效的哺乳动物种系转基因。
Transgenic Res. 2011 Feb;20(1):29-45. doi: 10.1007/s11248-010-9386-5. Epub 2010 Mar 30.
10
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.

大鼠基因打靶:进展与机遇。

Gene targeting in the rat: advances and opportunities.

机构信息

Department of Dermatology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.

出版信息

Trends Genet. 2010 Dec;26(12):510-8. doi: 10.1016/j.tig.2010.08.006. Epub 2010 Oct 1.

DOI:10.1016/j.tig.2010.08.006
PMID:20869786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2991520/
Abstract

The rat has long been a model favored by physiologists, pharmacologists and neuroscientists. However, over the past two decades, many investigators in these fields have turned to the mouse because of its gene modification technologies and extensive genomic resources. Although the genomic resources of the rat have nearly caught up, gene targeting has lagged far behind, limiting the value of the rat for many investigators. In the past two years, advances in transposon- and zinc finger nuclease (ZFN)-mediated gene knockout as well as the establishment and culturing of embryonic and inducible pluripotent stem cells have created new opportunities for rat genetic research. Here, we provide a high-level description and the potential uses of these new technologies for investigators using the rat for biomedical research.

摘要

大鼠长期以来一直是生理学家、药理学家和神经科学家所青睐的模型。然而,在过去的二十年中,由于其基因修饰技术和广泛的基因组资源,这些领域的许多研究人员都转向了小鼠。尽管大鼠的基因组资源已近赶上,但基因靶向技术却远远落后,这限制了大鼠在许多研究人员中的应用价值。在过去的两年中,转座子和锌指核酸酶(ZFN)介导的基因敲除技术的进步以及胚胎和诱导多能干细胞的建立和培养为大鼠遗传研究创造了新的机会。在这里,我们为使用大鼠进行生物医学研究的研究人员提供了这些新技术的高级描述和潜在用途。