Genome editing is critical for the development of tools that provide inroads into understanding the mechanisms underlying many biological processes, including development and disease. In addition to various methods applied in several model organisms, CRISPR/Cas9-based genome editing has emerged as a powerful technology that both broadens and accelerates genome editing in the last decade. CRISPR/Cas9 tools allow efficient modulation of both genetic and epigenetic structures within a cell or an organism. These tools can be utilized not only for deletion and insertion of sequences within the genome, but also for targeting and recruitment of various modulators into specific loci. Within the wealth of currently developed methods, the CRISPR/Cas9 realm constitutes a valuable addition for designing screens that address numerous bio/medical questions. However, it is challenging to design, adapt, modulate, and deliver the epi/genome editing tools into the given cell or organism. Depending on the model system and/or disease process, the methodology could be complicated, requiring careful optimization. In order to enhance the accessibility and utility of genome editing approaches across bio/medical sciences, it is necessary to collect and detail those applications that have been successful. This Methods Collection highlights different epi/genome editing approaches and methods utilized by leading experts to understand, model, treat and/or modulate the mechanisms involved in development and disease processes to advance such applications across the biomedical sciences.
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Cited by 10
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2023
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Harald Hartweger1, Rajeev Gautam2, Yoshiaki Nishimura2, Fabian Schmidt3,5, Kai-Hui Yao1, Amelia Escolano1,6, Mila Jankovic1, Malcolm A. Martin2, Michel C. Nussenzweig1,4
1Laboratory of Molecular Immunology, The Rockefeller University, 2Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 3Laboratory of Retrovirology, The Rockefeller University, 4Howard Hughes Medical Institute, The Rockefeller University, 5Laboratory of Applied Virology and Precision Medicine, King Abdullah University of Science and Technology (KAUST), 6Vaccine and Immunotherapy Center, Wistar Institute
Ablating target genes in hepatocytes with Cre-recombinase transgenic Plasmodium
Samarchith Kurup*1
1University of Georgia