Optimizing Gene Editing with PARP1 CRISPR Plasmids 


Conceptual multicolored image of CRISPR gene editing technology on a dark background with geometric figures.

PARP1 CRISPR Plasmids provide researchers with cutting edge tools for refining cell transfection and gene editing protocols.

Santa Cruz Biotechnology, Inc.

Gene editing is revolutionizing the understanding of health and disease, providing researchers with vast opportunities to advance the development of novel treatment approaches. Traditionally, researchers used various methods to introduce double strand breaks (DSBs) into the genome, including transactivator-like effectors, meganucleases, and zinc finger nucleases. While useful, these techniques are limited in that they are time and labor intensive, less efficient, and can have unintended effects. In contrast, the clustered regularly interspaced short palindromic repeat (CRISPR)-associated protein-9 (Cas9) system (CRISPR/Cas9) is among the most sensitive and efficient methods for creating DNA DSBs, making it the leading gene editing technology. 

CRISPR/Cas9 is a naturally occurring immune protective process that bacteria use to destroy foreign genetic material.1 Researchers repurposed the CRISPR/Cas9 system for genetic engineering applications in mammalian cells, exploiting the molecular processes that introduce DSBs in specific sections of DNA, which are then repaired to turn certain genes on or off, or to correct genomic errors with extraordinary precision.2,3 This technology’s applications are far reaching, from cell culture and animal models to translational research that focuses on correcting genetic mutations in diseases such as cancer, hemophilia, and sickle cell disease.4

Researchers exploit plasmids, the small, closed circular DNA strands native to bacteria, as delivery vehicles in CRISPR/Cas9 gene editing protocols. Plasmids shuttle the CRISPR/Cas9 gene editing components to target cells and can be manipulated to control gene editing activity, including targeting multiple genes at a time. Plasmids can also deliver gene repair instructions and machinery. For example, poly (ADP-ribose) polymerase 1 (PARP1) is an enzyme that drives DNA repair and transcription.5 It is a critical aspect of CRISPR/Cas9 gene editing technology in part because it helps repair the DSBs created by the CRISPR/Cas9 system. PARP1 CRISPR plasmids can edit, knockout, or upregulate PARP1 gene expression depending on the specific instructions encoded in the plasmid. 

Given the fundamental role that CRISPR/Cas9 plasmids play in gene editing processes, plasmid quality is a key consideration for safe, effective, and reliable gene editing. Santa Cruz Biotechnology, Inc.’s PARP1 CRISPR plasmids are optimized for research use that can lead to disease treatment advances. For example, the PARP1 homology-directed repair (HDR) plasmid exploits the HDR pathway that enables precise DNA repair at the location of the CRISPR/Cas9 DSB site according to a targeted repair template. Moreover, the HDR plasmid can be engineered to include a gene that induces fluorescence, providing researchers with visual confirmation of successful transfection. The inclusion of an antibiotic resistance gene also allows researchers to select for cells that carry DSBs. For researchers engaged in gene editing, knowing whether cells have been successfully transfected and being able to select the specific cells that have DSBs is critical. Overall, such solutions help scientists take the guesswork out of sensitive and multi-step gene editing techniques, optimize workflows, and produce consistent and reliable data.

References

  1. Jinek M, et al. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science. 2012;337:816–21. 
  2. Ran FA, et al. Genome engineering using the CRISPR-Cas9 system. Nat Protoc. 2013;8:2281-2308.
  3. Hsu PD, et al. Development and applications of CRISPR-Cas9 for genome editing. Cell. 2014; 157:1262-78.
  4. Huang K, et al. In vivo delivery of CRISPR-Cas9 genome editing components for therapeutic applications. Biomaterials. 2022;291:121876.
  5. Ko HL, Ren EC. Functional aspects of PARP1 in DNA repair and transcription. Biomolecules. 2012;2(4):524-48. 
Santa Cruz Biotechnology Inc logo

Leave a Reply

Your email address will not be published. Required fields are marked *