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通过 和 基因编辑受精卵,高效快速地生成相关疾病的小鼠模型。

Efficient and Fast Generation of Relevant Disease Mouse Models by and Gene Editing of Zygotes.

机构信息

Molecular and Translational Oncology Division, Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain.

Instituto de Investigación Sanitaria Hospital 12 de octubre (imas12), Madrid, Spain.

出版信息

CRISPR J. 2022 Jun;5(3):422-434. doi: 10.1089/crispr.2022.0013.

DOI:10.1089/crispr.2022.0013
PMID:35686982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9233508/
Abstract

Knockout mice for human disease-causing genes provide valuable models in which new therapeutic approaches can be tested. Electroporation of genome editing tools into zygotes, or within oviducts, allows for the generation of targeted mutations in a shorter time. We have generated mouse models deficient in genes involved in metabolic rare diseases (Primary Hyperoxaluria Type 1 Pyruvate Kinase Deficiency) or in a tumor suppressor gene (). Pairs of guide RNAs were designed to generate controlled deletions that led to the absence of protein. or ribonucleoprotein (RNP) electroporation rendered more than 90% and 30% edited newborn animals, respectively. Mice lines with edited alleles were established and disease hallmarks have been verified in the three models that showed a high consistency of results and validating RNP electroporation into zygotes as an efficient technique for disease modeling without the need to outsource to external facilities.

摘要

敲除人类致病基因的小鼠为新的治疗方法提供了有价值的模型,可以在这些模型中进行测试。将基因组编辑工具电穿孔到受精卵或输卵管中,可以在更短的时间内产生靶向突变。我们已经成功构建了几种代谢罕见病(1 型原发性高草酸尿症和丙酮酸激酶缺乏症)或抑癌基因()的基因敲除小鼠模型。设计了两对向导 RNA 来产生导致蛋白缺失的可控缺失。分别对 或核糖核蛋白(RNP)进行电穿孔,使超过 90%和 30%的新生动物发生编辑。建立了具有编辑等位基因的小鼠系,并在三种模型中验证了疾病特征,这些模型的结果具有高度一致性,证明了将 RNP 电穿孔到受精卵中是一种有效的疾病建模技术,无需外包给外部机构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/32ce52188e31/crispr.2022.0013_figure7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/6d17346f5520/crispr.2022.0013_figure1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/e6c6c47844a7/crispr.2022.0013_figure2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/16ae81fe0292/crispr.2022.0013_figure3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/95e20a67dbc8/crispr.2022.0013_figure4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/926908571ffa/crispr.2022.0013_figure5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/af6ae79fa04d/crispr.2022.0013_figure6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/32ce52188e31/crispr.2022.0013_figure7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/6d17346f5520/crispr.2022.0013_figure1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/e6c6c47844a7/crispr.2022.0013_figure2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/16ae81fe0292/crispr.2022.0013_figure3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/95e20a67dbc8/crispr.2022.0013_figure4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/926908571ffa/crispr.2022.0013_figure5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/af6ae79fa04d/crispr.2022.0013_figure6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eaf/9233508/32ce52188e31/crispr.2022.0013_figure7.jpg

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