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利用CRISPR/Cas9介导的胚胎干细胞靶向技术生成两种去甲肾上腺素能特异性多巴胺-β-羟化酶-FLPo基因敲入小鼠

Generation of Two Noradrenergic-Specific Dopamine-Beta-Hydroxylase-FLPo Knock-In Mice Using CRISPR/Cas9-Mediated Targeting in Embryonic Stem Cells.

作者信息

Sun Jenny J, Ray Russell

机构信息

Department of Neuroscience, Baylor College of Medicine, Houston, Texas, United States of America.

McNair Medical Institute, Baylor College of Medicine, Houston, Texas, United States of America.

出版信息

PLoS One. 2016 Jul 21;11(7):e0159474. doi: 10.1371/journal.pone.0159474. eCollection 2016.

Abstract

CRISPR/Cas9 mediated DNA double strand cutting is emerging as a powerful approach to increase rates of homologous recombination of large targeting vectors, but the optimization of parameters, equipment and expertise required remain barriers to successful mouse generation by single-step zygote injection. Here, we sought to apply CRISPR/Cas9 methods to traditional embryonic stem (ES) cell targeting followed by blastocyst injection to overcome the common issues of difficult vector construction and low targeting efficiency. To facilitate the study of noradrenergic function, which is implicated in myriad behavioral and physiological processes, we generated two different mouse lines that express FLPo recombinase under control of the noradrenergic-specific Dopamine-Beta-Hydroxylase (DBH) gene. We found that by co-electroporating a circular vector expressing Cas9 and a locus-specific sgRNA, we could target FLPo to the DBH locus in ES cells with shortened 1 kb homology arms. Two different sites in the DBH gene were targeted; the translational start codon with 6-8% targeting efficiency, and the translational stop codon with 75% targeting efficiency. Using this approach, we established two mouse lines with DBH-specific expression of FLPo in brainstem catecholaminergic populations that are publically available on MMRRC (MMRRC_041575-UCD and MMRRC_041577-UCD). Altogether, this study supports simplified, high-efficiency Cas9/CRISPR-mediated targeting in embryonic stem cells for production of knock-in mouse lines in a wider variety of contexts than zygote injection alone.

摘要

CRISPR/Cas9介导的DNA双链切割正成为一种提高大型靶向载体同源重组率的强大方法,但所需参数、设备和专业知识的优化仍然是通过单步受精卵注射成功培育小鼠的障碍。在此,我们试图将CRISPR/Cas9方法应用于传统的胚胎干细胞(ES细胞)靶向,随后进行囊胚注射,以克服载体构建困难和靶向效率低的常见问题。为了便于研究涉及无数行为和生理过程的去甲肾上腺素能功能,我们培育了两种不同的小鼠品系,它们在去甲肾上腺素能特异性多巴胺-β-羟化酶(DBH)基因的控制下表达FLPo重组酶。我们发现,通过共电穿孔表达Cas9的环状载体和位点特异性sgRNA,我们可以将FLPo靶向ES细胞中的DBH位点,同源臂缩短至1 kb。我们靶向了DBH基因中的两个不同位点;翻译起始密码子的靶向效率为6-8%,翻译终止密码子的靶向效率为75%。使用这种方法,我们建立了两个小鼠品系,其脑干儿茶酚胺能群体中FLPo具有DBH特异性表达,可在MMRRC上公开获得(MMRRC_041575-UCD和MMRRC_041577-UCD)。总之,本研究支持在胚胎干细胞中进行简化、高效的Cas9/CRISPR介导的靶向,以在比单独受精卵注射更广泛的背景下生产敲入小鼠品系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e423/4956144/97d8cc513711/pone.0159474.g001.jpg

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