The current gold-standard for genetic lineage tracing in transgenic mice is based on cell-type specific expression of Cre recombinase. As an alternative, we developed a cell-type specific CRISPR/spCas9 system for lineage tracing. This method relies on RNA polymerase II promoter driven self-cleaving guide RNAs (scgRNA) to achieve tissue-specificity. To demonstrate proof-of-principle for this approach a transgenic mouse was generated harbouring a knock-in of a scgRNA into the Cytokeratin 14 (Krt14) locus. Krt14 expression marks the stem cells of squamous epithelium in the skin and oral mucosa. The scgRNA targets a Stop cassette preceding a fluorescent reporter in the Ai9-tdtomato mouse. Ai9-tdtomato reporter mice harbouring this allele along with a spCas9 transgene demonstrated precise marking of the Krt14 lineage. We conclude that RNA polymerase II promoter driven scgRNAs enable the use of CRISPR/spCas9 for genetic lineage tracing.
In vivo tracing of the Cytokeratin 14 lineages using self-cleaving guide RNAs and CRISPR/Cas9.
利用自切割向导 RNA 和 CRISPR/Cas9 对细胞角蛋白 14 谱系进行体内追踪
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作者:Tiyaboonchai Amita, Wakefield Leslie, Vonada Anne, May Catherine L, Dorrell Craig, Enicks David, Sairavi Anusha, Kaestner Klaus H, Grompe Markus
| 期刊: | Developmental Biology | 影响因子: | 2.100 |
| 时间: | 2023 | 起止号: | 2023 Dec;504:120-127 |
| doi: | 10.1016/j.ydbio.2023.09.011 | 研究方向: | 细胞生物学 |
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