In vivo tracing of the Cytokeratin 14 lineages using self-cleaving guide RNAs and CRISPR/Cas9

Dev Biol. 2023 Dec:504:120-127. doi: 10.1016/j.ydbio.2023.09.011. Epub 2023 Oct 7.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CRISPR-Cas Systems* / genetics
  • Integrases / genetics
  • Keratin-14 / genetics
  • Keratin-14 / metabolism
  • Mice
  • Mice, Transgenic
  • Promoter Regions, Genetic / genetics
  • RNA Polymerase II* / genetics
  • RNA Polymerase II* / metabolism

Substances

  • Integrases
  • Keratin-14
  • RNA Polymerase II
  • Krt14 protein, mouse