| Literature DB >> 32710419 |
Solmaz Khosravi1, Steven Dreissig1, Patrick Schindele2, Felix Wolter2, Twan Rutten1, Holger Puchta3, Andreas Houben4.
Abstract
Chromatin organization is highly dynamic in living cells. Therefore, it might have a regulatory role over biological mechanisms like transcription, replication, and DNA repair. To elucidate how these mechanisms are regulated, it is required to establish imaging methods to visualize the chromatin dynamic in living cells. Here, we provide a protocol for a live plant cell imaging technique based on application of two orthologs of the bacterial clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (Cas9) from Streptococcus pyogenes and Staphylococcus aureus. This technique uses the inactive variants of Cas9 combined with different fluorescent proteins (GFP and mRuby) and telomere-specific guide RNA to target telomeric repeats in Nicotiana benthamiana. Our immuno-FISH data revealed that signals arising from the CRISPR/dCas9 method are specifically belonging to telomeric regions.Entities:
Keywords: CRISPR/dCas9; Chromatin organization; Guide RNA; Live-cell imaging; Nicotiana benthamiana; Telomere
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Year: 2020 PMID: 32710419 DOI: 10.1007/978-1-0716-0712-1_20
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745