Photocaged Hoechst Enables Subnuclear Visualization and Cell Selective Staining of DNA in vivo

Selective targeting of DNA by means of fluorescent labeling has become a mainstay in the life sciences. While genetic engineering serves as a powerful technique and allows the visualization of nucleic acid by using DNA‐targeting fluorescent fusion proteins in a cell‐type‐ and subcellular‐specific manner, it relies on the introduction of foreign genes. On the other hand, DNA‐binding small fluorescent molecules can be used without genetic engineering, but they are not spatially restricted. Herein, we report a photocaged version of the DNA dye Hoechst33342 (pcHoechst), which can be uncaged by using UV to blue light for the selective staining of chromosomal DNA in subnuclear regions of live cells. Expanding its application to a vertebrate model organism, we demonstrate uncaging in epithelial cells and short‐term cell tracking in vivo in zebrafish. We envision pcHoechst as a valuable tool for targeting and interrogating DNA with precise spatiotemporal resolution in living cells and wild‐type organisms.

[1]  D. Torrents,et al.  Extrachromosomal circular DNA drives oncogenic genome remodeling in neuroblastoma , 2019, Nature Genetics.

[2]  A. Moskalensky,et al.  Long-wavelength photoremovable protecting groups: On the way to in vivo application , 2019, Computational and structural biotechnology journal.

[3]  M. Kellermayer,et al.  Green-Light Activatable, Water-Soluble Red-Shifted Coumarin Photocages. , 2019, Organic letters.

[4]  S. Hell,et al.  Rhodamine–Hoechst positional isomers for highly efficient staining of heterochromatin , 2018, Chemical science.

[5]  Z. Gartner,et al.  Cell-Specific Chemical Delivery Using a Selective Nitroreductase-Nitroaryl Pair. , 2018, ACS chemical biology.

[6]  Yoav Shechtman,et al.  Observing DNA in live cells. , 2018, Biochemical Society transactions.

[7]  G. Lukinavičius,et al.  The Use of Hoechst Dyes for DNA Staining and Beyond , 2018 .

[8]  Yevgenia Kozorovitskiy,et al.  Photoactivatable drugs for nicotinic optopharmacology , 2018, Nature Methods.

[9]  P. Klán,et al.  In Search of the Perfect Photocage: Structure-Reactivity Relationships in meso-Methyl BODIPY Photoremovable Protecting Groups. , 2017, Journal of the American Chemical Society.

[10]  S. Hell,et al.  Fluorescence nanoscopy in cell biology , 2017, Nature Reviews Molecular Cell Biology.

[11]  Mustafa Mir,et al.  Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9 , 2017, Nature Communications.

[12]  Robert F. Siliciano,et al.  Nuclear landscape of HIV-1 infection and integration , 2016, Nature Reviews Microbiology.

[13]  Bo Huang,et al.  Imaging Specific Genomic DNA in Living Cells. , 2016, Annual review of biophysics.

[14]  Shaojie Zhang,et al.  Multiplexed labeling of genomic loci with dCas9 and engineered sgRNAs using CRISPRainbow , 2016, Nature Biotechnology.

[15]  Stefan W. Hell,et al.  SiR–Hoechst is a far-red DNA stain for live-cell nanoscopy , 2015, Nature Communications.

[16]  Shaojie Zhang,et al.  Multicolor CRISPR labeling of chromosomal loci in human cells , 2015, Proceedings of the National Academy of Sciences.

[17]  Chunhui Huang,et al.  DNA gated photochromism and fluorescent switch in a thiazole orange modified diarylethene. , 2014, Chemical communications.

[18]  Tobias Moser,et al.  A new probe for super-resolution imaging of membranes elucidates trafficking pathways , 2014, The Journal of cell biology.

[19]  Keiko Kuwata,et al.  Hoechst tagging: a modular strategy to design synthetic fluorescent probes for live-cell nucleus imaging. , 2014, Chemical communications.

[20]  Luke A. Gilbert,et al.  Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System , 2013, Cell.

[21]  R. Givens,et al.  Photoremovable Protecting Groups in Chemistry and Biology: Reaction Mechanisms and Efficacy , 2012, Chemical reviews.

[22]  M. Cristina Cardoso,et al.  Targeted manipulation of heterochromatin rescues MeCP2 Rett mutants and re-establishes higher order chromatin organization , 2012, Nucleic acids research.

[23]  D. Berdnikova,et al.  Photoinduced in situ generation of a DNA-binding benzothiazoloquinolinium derivative. , 2012, Chemical communications.

[24]  Amy Hu,et al.  Selective esterase–ester pair for targeting small molecules with cellular specificity , 2012, Proceedings of the National Academy of Sciences.

[25]  G. Ya. Wiederschain,et al.  The Molecular Probes handbook. A guide to fluorescent probes and labeling technologies , 2011, Biochemistry (Moscow).

[26]  Martin Purschke,et al.  Phototoxicity of Hoechst 33342 in time-lapse fluorescence microscopy , 2010, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

[27]  R. Köster,et al.  The centrosome neither persistently leads migration nor determines the site of axonogenesis in migrating neurons in vivo , 2010, The Journal of cell biology.

[28]  Jan Ellenberg,et al.  Molecular crowding affects diffusion and binding of nuclear proteins in heterochromatin and reveals the fractal organization of chromatin , 2009, The EMBO journal.

[29]  Tobias Meckel,et al.  Live cell imaging of repetitive DNA sequences via GFP-tagged polydactyl zinc finger proteins , 2007, Nucleic acids research.

[30]  J. Ellenberg,et al.  Measuring structural dynamics of chromosomes in living cells by fluorescence microscopy. , 2007, Methods.

[31]  Heinrich Leonhardt,et al.  DNA labeling in living cells , 2005, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[32]  D. Häder,et al.  UV-induced DNA damage and repair: a review , 2002, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

[33]  D. Pinkel,et al.  Incidence of chromosome aberrations in mammalian sperm stained with Hoechst 33342 and UV-laser irradiated during flow sorting. , 1987, Mutation research.

[34]  R. Dickerson,et al.  Binding of Hoechst 33258 to the minor groove of B-DNA. , 1987, Journal of molecular biology.

[35]  J. Davies,et al.  Molecular Biology of the Cell , 1983, Bristol Medico-Chirurgical Journal.

[36]  P. Olive,et al.  Cytotoxicity, Mutagenicity and DNA damage by Hoechst 33342. , 1982, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[37]  R. Tsien A non-disruptive technique for loading calcium buffers and indicators into cells , 1981, Nature.