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CRISPR interference provides increased cell type-specificity compared to the Cre-loxP system.
Laster, Dominique J; Akel, Nisreen S; Hendrixson, James A; James, Alicen; Crawford, Julie A; Fu, Qiang; Berryhill, Stuart B; Thostenson, Jeff D; Nookaew, Intawat; O'Brien, Charles A; Onal, Melda.
Afiliação
  • Laster DJ; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Akel NS; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Hendrixson JA; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • James A; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Crawford JA; Center for Musculoskeletal Disease Research (CMDR), University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Fu Q; Division of Endocrinology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Berryhill SB; Center for Musculoskeletal Disease Research (CMDR), University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Thostenson JD; Division of Endocrinology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Nookaew I; Center for Musculoskeletal Disease Research (CMDR), University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • O'Brien CA; Division of Endocrinology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
  • Onal M; Department of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
iScience ; 26(8): 107428, 2023 Aug 18.
Article em En | MEDLINE | ID: mdl-37575184
ABSTRACT
Cre-mediated recombination is frequently used for cell type-specific loss of function (LOF) studies. A major limitation of this system is recombination in unwanted cell types. CRISPR interference (CRISPRi) has been used effectively for global LOF in mice. However, cell type-specific CRISPRi, independent of recombination-based systems, has not been reported. To test the feasibility of cell type-specific CRISPRi, we produced two novel knock-in mouse models that achieve gene suppression when used together one expressing dCas9KRAB under the control of a cell type-specific promoter and the other expressing a single guide RNA from a safe harbor locus. We then compared the phenotypes of mice in which the same gene was targeted by either CRISPRi or the Cre-loxP system, with cell specificity conferred by Dmp1 regulatory elements in both cases. We demonstrate that CRISPRi is effective for cell type-specific LOF and that it provides improved cell type-specificity compared to the Cre-loxP system.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos