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优化用于CRISPR/Cas9系统应用的胚胎采集方法,并使用该方法生成福库汀基因敲除大鼠。

Optimizing Embryo Collection for Application of CRISPR/Cas9 System and Generation of Fukutin Knockout Rat Using This Method.

作者信息

Seol Dong-Won, Park Byoung-Jin, Koo Deog-Bon, Kim Ji-Su, Jeon Yong-Hyun, Lee Jae-Eon, Park Joon-Suk, Jang Hoon, Wee Gabbine

机构信息

Preclinical Research Center, Daegu-Gyeongbuk Medical Innovation Foundation (KMEDIHUB), Daegu 41061, Republic of Korea.

Non-Clinical Evaluation Center, Osong Medical Innovation Foundation (KBIO Health), Cheongju 28160, Republic of Korea.

出版信息

Curr Issues Mol Biol. 2024 Apr 23;46(5):3752-3762. doi: 10.3390/cimb46050234.

Abstract

Rat animal models are widely used owing to their relatively superior cognitive abilities and higher similarity compared with mouse models to human physiological characteristics. However, their use is limited because of difficulties in establishing embryonic stem cells and performing genetic modifications, and insufficient embryological research. In this study, we established optimal superovulation and fertilized-egg transfer conditions, including optimal hormone injection concentration (≥150 IU/kg of PMSG and hCG) and culture medium (mR1ECM), to obtain high-quality zygotes and establish in vitro fertilization conditions for rats. Next, sgRNA with optimal targeting activity was selected by performing PCR analysis and the T7E1 assay, and the CRISPR/Cas9 system was used to construct a rat model for muscular dystrophy by inducing a deficiency in the gene without any off-target effect detected. The production of knockout rats was phenotypically confirmed by observing a drop-in body weight to one-third of that of the control group. In summary, we succeeded in constructing the first muscular dystrophy disease rat model using the CRISPR/CAS9 system for increasing future prospects of producing various animal disease models and encouraging disease research using rats.

摘要

大鼠动物模型因其相对优越的认知能力以及与小鼠模型相比在生理特征上与人类具有更高的相似性而被广泛使用。然而,由于建立胚胎干细胞和进行基因改造存在困难以及胚胎学研究不足,其应用受到限制。在本研究中,我们建立了最佳的超排卵和受精卵移植条件,包括最佳激素注射浓度(≥150 IU/kg的孕马血清促性腺激素和人绒毛膜促性腺激素)和培养基(mR1ECM),以获得高质量的受精卵并建立大鼠体外受精条件。接下来,通过进行PCR分析和T7E1检测选择具有最佳靶向活性的sgRNA,并使用CRISPR/Cas9系统通过诱导该基因缺陷来构建肌营养不良大鼠模型,未检测到任何脱靶效应。通过观察体重降至对照组的三分之一,对敲除大鼠的产生进行了表型确认。总之,我们成功地使用CRISPR/CAS9系统构建了首个肌营养不良疾病大鼠模型,以增加未来生产各种动物疾病模型的前景,并鼓励使用大鼠进行疾病研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce09/11120416/36200456df5b/cimb-46-00234-g001.jpg

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