| Literature DB >> 36255617 |
Lena Hess1, Verena Moos1, Christian Seiser2.
Abstract
Class I histone deacetylases (HDACs) are important regulators of cellular functions in health and disease. HDAC1, HDAC2, HDAC3, and HDAC8 are promising targets for the treatment of cancer, neurological, and immunological disorders. These enzymes have both catalytic and non-catalytic functions in the regulation of gene expression. We here describe the generation of a genetic toolbox by the CRISPR/Cas9 methodology in nearly haploid human tumor cells. This novel model system allows to discriminate between catalytic and structural functions of class I HDAC enzymes and to mimic the treatment with specific HDAC inhibitors.Entities:
Keywords: CRISPR/Cas9; HDAC inactivation; HDAC inhibition; Knock-in; Knockout; Transgenic cells
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Year: 2023 PMID: 36255617 DOI: 10.1007/978-1-0716-2788-4_4
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745