biGMamAct:高效的CRISPR/Cas9介导对接大型功能性DNA货物在ACTB位置
Martin Pelosse1, Marco Marcia1
1EMBL Grenoble, European Molecular Biology Laboratory, 71 avenue des Martyrs, Grenoble Cedex 9 CS 90181, 38042, France.
Synthetic biology (Oxford, England)
|March 11, 2025
概括
研究人员开发了biGMamAct,这是一个新的系统,可以有效地将大型DNA有效载荷集成到哺乳动物基因组中. 这一突破使得能够创建稳定的细胞系用于先进的分子和细胞生物学研究.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 基因组工程是基因组工程.
背景情况:
- 先进的分子和细胞生物学研究需要在现场可视化宏分子复合体和代谢途径.
- 通过基因组编辑生成具有大量DNA载荷的稳定真核细胞系是具有挑战性的.
研究的目的:
- 开发一个系统,以高效,标准化组装和基因组集成哺乳动物细胞的大型DNA货物.
- 克服在生成稳定的细胞系的局限性,用于复杂的分子成像和功能研究.
主要方法:
- 设计了biGMamAct,一个模块化哺乳动物表达等离子体系统用于标准化克隆.
- 使用Cas9/sgRNA对在ACTB位点进行同源独立的向插入.
- 在基因组中组装和集成大型DNA货物 (例如18.3kb).
主要成果:
- 成功生成了一种稳定的细胞系,其DNA载荷为18.3kb,表达了6种光标记蛋白质.
- 证明了五个不同的亚细胞区的同时可视化.
- 协议使单个克隆的特征能够在从in silico设计开始的6周内实现.
结论:
- 该biGMamAct系统提供了一个高效的方法,用于将大型遗传模块集成到哺乳动物基因组中.
- 这有助于创建先进的细胞模型,用于多尺度结构功能研究和现场成像.
- 该协议可供具有标准分子生物学和细胞培养专业知识的研究人员使用.
相关概念视频
CRISPR
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced Short...
Homologous Recombination
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
Conservative Site-specific Recombination and Phase Variation
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
CRISPR and crRNAs
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
CRISPR/Cas9 Genome Editing
The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...


