Methyl β-Cyclodextrin-sperm-mediated gene editing (MBCD-SMGE): a simple and efficient method for targeted mutant mouse production.

IF 3.7 3区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Biological Procedures Online Pub Date : 2024-01-26 DOI:10.1186/s12575-024-00230-9
Parisa Moradbeigi, Sara Hosseini, Mohammad Salehi, Asghar Mogheiseh
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Abstract

Background: Generating targeted mutant mice is a crucial technology in biomedical research. This study focuses on optimizing the CRISPR/Cas9 system uptake into sperm cells using the methyl β-cyclodextrin-sperm-mediated gene transfer (MBCD-SMGT) technique to generate targeted mutant blastocysts and mice efficiently. Additionally, the present study elucidates the roles of cholesterol and reactive oxygen species (ROS) in the exogenous DNA uptake by sperm.

Results: In this study, B6D2F1 mouse sperm were incubated in the c-TYH medium with different concentrations of MBCD (0, 0.75, 1, and 2 mM) in the presence of 20 ng/µl pCAG-eCas9-GFP-U6-gRNA (pgRNA-Cas9) for 30 min. Functional parameters, extracellular ROS, and the copy numbers of internalized plasmid per sperm cell were evaluated. Subsequently, in vitro fertilization (IVF) was performed and fertilization rate, early embryonic development, and transfection rate were assessed. Finally, our study investigated the potential of the MBCD-SMGT technique in combination with the CRISPR-Cas9 system, referred to as MBCD-SMGE (MBCD-sperm-mediated gene editing), for generating targeted mutant blastocysts and mice. Results indicated that cholesterol removal from the sperm membrane using MBCD resulted in a premature acrosomal reaction, an increase in extracellular ROS levels, and a dose-dependent influence on the copy numbers of the internalized plasmids per sperm cell. Moreover, the MBCD-SMGT technique led to a larger population of transfected motile sperm and a higher production rate of GFP-positive blastocysts. Additionally, the current study validated the targeted indel in blastocyst and mouse derived from MBCD-SMGE technique.

Conclusion: Overall, this study highlights the significant potential of the MBCD-SMGE technique for generating targeted mutant mice. It holds enormous promise for modeling human diseases and improving desirable traits in animals.

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甲基β-环糊精-精子介导的基因编辑(MBCD-SMGE):一种简单高效的靶向突变小鼠生产方法。
背景:产生靶向突变小鼠是生物医学研究中的一项重要技术。本研究的重点是利用甲基β-环糊精-精子介导的基因转移(MBCD-SMGT)技术优化CRISPR/Cas9系统在精子细胞中的吸收,从而高效地产生靶向突变囊胚和小鼠。此外,本研究还阐明了胆固醇和活性氧(ROS)在精子吸收外源 DNA 过程中的作用:本研究将 B6D2F1 小鼠精子置于含有不同浓度 MBCD(0、0.75、1 和 2 mM)的 c-TYH 培养基中,在 20 ng/µl pCAG-eCas9-GFP-U6-gRNA (pgRNA-Cas9)存在下培养 30 分钟。对功能参数、细胞外 ROS 和每个精子细胞内化质粒的拷贝数进行了评估。随后,进行了体外受精(IVF),并对受精率、早期胚胎发育和转染率进行了评估。最后,我们的研究调查了 MBCD-SMGT 技术与 CRISPR-Cas9 系统结合(称为 MBCD-SMGE(MBCD-精子介导的基因编辑))生成靶向突变囊胚和小鼠的潜力。结果表明,使用 MBCD 去除精子膜上的胆固醇会导致过早的顶体反应、细胞外 ROS 水平升高,并对每个精子细胞内化质粒的拷贝数产生剂量依赖性影响。此外,MBCD-SMGT 技术还能产生更多的转染运动精子和更高的 GFP 阳性囊胚生产率。此外,本研究还验证了 MBCD-SMGE 技术在囊胚和小鼠中产生的靶向吲哚:总之,本研究强调了 MBCD-SMGE 技术在产生靶向突变小鼠方面的巨大潜力。它为人类疾病建模和改善动物的理想性状带来了巨大希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biological Procedures Online
Biological Procedures Online 生物-生化研究方法
CiteScore
10.50
自引率
0.00%
发文量
16
审稿时长
>12 weeks
期刊介绍: iological Procedures Online publishes articles that improve access to techniques and methods in the medical and biological sciences. We are also interested in short but important research discoveries, such as new animal disease models. Topics of interest include, but are not limited to: Reports of new research techniques and applications of existing techniques Technical analyses of research techniques and published reports Validity analyses of research methods and approaches to judging the validity of research reports Application of common research methods Reviews of existing techniques Novel/important product information Biological Procedures Online places emphasis on multidisciplinary approaches that integrate methodologies from medicine, biology, chemistry, imaging, engineering, bioinformatics, computer science, and systems analysis.
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