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- W4311764526 abstract "Rats were more frequently used than mice to model human disease before mouse embryonic stem cells (mESCs) revolutionized genetic engineering in mice. Rat ESCs (rESCs) were first reported over 10 years ago, yet they are not as frequently used as mESCs. CRISPR-based gene editing in zygotes is widely used in rats but is limited by the difficulty of inserting or replacing DNA sequences larger than about 10 kb. We report here the generation of germline-competent rESC lines from several rat strains. These rESC lines maintain their potential for germline transmission after serial targeting with bacterial artificial chromosome (BAC)-based targeting vectors, and CRISPR-Cas9 cutting can increase targeting efficiency. Using these methods, we have successfully replaced entire rat genes spanning up to 101 kb with the human ortholog." @default.
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- W4311764526 date "2023-01-01" @default.
- W4311764526 modified "2023-10-01" @default.
- W4311764526 title "Production of large, defined genome modifications in rats by targeting rat embryonic stem cells" @default.
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- W4311764526 doi "https://doi.org/10.1016/j.stemcr.2022.11.012" @default.
- W4311764526 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36525967" @default.
- W4311764526 hasPublicationYear "2023" @default.
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