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利用CRISPR/Cas9技术并显微注射到受精卵中高效制备肌肉生长抑制素基因敲除绵羊

Efficient Generation of Myostatin Knock-Out Sheep Using CRISPR/Cas9 Technology and Microinjection into Zygotes.

作者信息

Crispo M, Mulet A P, Tesson L, Barrera N, Cuadro F, dos Santos-Neto P C, Nguyen T H, Crénéguy A, Brusselle L, Anegón I, Menchaca A

机构信息

Unidad de Animales Transgénicos y de Experimentación (UATE), Institut Pasteur de Montevideo, Montevideo, Uruguay.

INSERM UMR 1064, Center for Research in Transplantation and Immunology-ITUN, Nantes, France.

出版信息

PLoS One. 2015 Aug 25;10(8):e0136690. doi: 10.1371/journal.pone.0136690. eCollection 2015.

Abstract

While CRISPR/Cas9 technology has proven to be a valuable system to generate gene-targeted modified animals in several species, this tool has been scarcely reported in farm animals. Myostatin is encoded by MSTN gene involved in the inhibition of muscle differentiation and growth. We determined the efficiency of the CRISPR/Cas9 system to edit MSTN in sheep and generate knock-out (KO) animals with the aim to promote muscle development and body growth. We generated CRISPR/Cas9 mRNAs specific for ovine MSTN and microinjected them into the cytoplasm of ovine zygotes. When embryo development of CRISPR/Cas9 microinjected zygotes (n = 216) was compared with buffer injected embryos (n = 183) and non microinjected embryos (n = 173), cleavage rate was lower for both microinjected groups (P<0.05) and neither was affected by CRISPR/Cas9 content in the injected medium. Embryo development to blastocyst was not affected by microinjection and was similar among the experimental groups. From 20 embryos analyzed by Sanger sequencing, ten were mutant (heterozygous or mosaic; 50% efficiency). To obtain live MSTN KO lambs, 53 blastocysts produced after zygote CRISPR/Cas9 microinjection were transferred to 29 recipient females resulting in 65.5% (19/29) of pregnant ewes and 41.5% (22/53) of newborns. From 22 born lambs analyzed by T7EI and Sanger sequencing, ten showed indel mutations at MSTN gene. Eight showed mutations in both alleles and five of them were homozygous for indels generating out-of frame mutations that resulted in premature stop codons. Western blot analysis of homozygous KO founders confirmed the absence of myostatin, showing heavier body weight than wild type counterparts. In conclusion, our results demonstrate that CRISPR/Cas9 system was a very efficient tool to generate gene KO sheep. This technology is quick and easy to perform and less expensive than previous techniques, and can be applied to obtain genetically modified animal models of interest for biomedicine and livestock.

摘要

虽然CRISPR/Cas9技术已被证明是在多个物种中生成基因靶向修饰动物的有价值系统,但该工具在农场动物中的报道却很少。肌肉生长抑制素由MSTN基因编码,参与抑制肌肉分化和生长。我们确定了CRISPR/Cas9系统编辑绵羊MSTN基因并生成基因敲除(KO)动物的效率,旨在促进肌肉发育和身体生长。我们生成了针对绵羊MSTN的CRISPR/Cas9 mRNA,并将其显微注射到绵羊受精卵的细胞质中。当将显微注射CRISPR/Cas9的受精卵(n = 216)的胚胎发育与注射缓冲液的胚胎(n = 183)和未显微注射的胚胎(n = 173)进行比较时,两个显微注射组的卵裂率均较低(P<0.05),且均不受注射培养基中CRISPR/Cas9含量的影响。胚胎发育到囊胚不受显微注射的影响,且在各实验组中相似。通过桑格测序分析的20个胚胎中,有10个是突变体(杂合或嵌合体;效率为50%)。为了获得活的MSTN基因敲除羔羊,将受精卵CRISPR/Cas9显微注射后产生的53个囊胚移植到29只受体母羊中,怀孕母羊的比例为65.5%(19/29),新生羔羊的比例为41.5%(22/53)。通过T7EI和桑格测序分析的22只出生羔羊中,有10只在MSTN基因处出现插入缺失突变。8只在两个等位基因中均出现突变,其中5只为插入缺失的纯合子,产生了移码突变,导致提前出现终止密码子。对纯合基因敲除始祖羊的蛋白质免疫印迹分析证实没有肌肉生长抑制素,其体重比野生型羊更重。总之,我们的结果表明CRISPR/Cas9系统是生成基因敲除绵羊的非常有效的工具。该技术操作快速简便,比以前的技术成本更低,可用于获得生物医学和家畜领域感兴趣的转基因动物模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7db/4549068/1cbbaf0e5929/pone.0136690.g001.jpg

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