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Generation and characterization of inducible KRAB-dCas9 iPSCs from primates for cross-species CRISPRi.
Edenhofer, Fiona C; Térmeg, Anita; Ohnuki, Mari; Jocher, Jessica; Kliesmete, Zane; Briem, Eva; Hellmann, Ines; Enard, Wolfgang.
Afiliação
  • Edenhofer FC; Anthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians-Universität München, 82152 Planegg, Germany.
  • Térmeg A; Anthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians-Universität München, 82152 Planegg, Germany.
  • Ohnuki M; Anthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians-Universität München, 82152 Planegg, Germany.
  • Jocher J; Institute for the Advanced Study of Human Biology, Kyoto University, Kyoto 606-8501, Japan.
  • Kliesmete Z; Hakubi Center, Kyoto University, Kyoto 606-8501, Japan.
  • Briem E; Anthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians-Universität München, 82152 Planegg, Germany.
  • Hellmann I; Anthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians-Universität München, 82152 Planegg, Germany.
  • Enard W; Anthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians-Universität München, 82152 Planegg, Germany.
iScience ; 27(6): 110090, 2024 Jun 21.
Article em En | MEDLINE | ID: mdl-38947524
ABSTRACT
Comparisons of molecular phenotypes across primates provide unique information to understand human biology and evolution, and single-cell RNA-seq CRISPR interference (CRISPRi) screens are a powerful approach to analyze them. Here, we generate and validate three human, three gorilla, and two cynomolgus iPS cell lines that carry a dox-inducible KRAB-dCas9 construct at the AAVS1 locus. We show that despite variable expression levels of KRAB-dCas9 among lines, comparable downregulation of target genes and comparable phenotypic effects are observed in a single-cell RNA-seq CRISPRi screen. Hence, we provide valuable resources for performing and further extending CRISPRi in human and non-human primates.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article