HI-NESS: a family of genetically encoded DNA labels based on a bacterial nucleoid-associated protein

Author:

Rashid Fatema-Zahra M12,Mahlandt Eike3,van der Vaart Michiel4,Boer Daphne E C5,Varela Alvarez Monica4,Henneman Bram1,Brocken Daan J W1,Voskamp Patrick6,Blok Anneloes J1,Shimizu Thomas S7,Meijer Annemarie H4,Luijsterburg Martijn S5,Goedhart Joachim3ORCID,Crémazy Frédéric G E1,Dame Remus T12ORCID

Affiliation:

1. Macromolecular Biochemistry, Leiden Institute of Chemistry, Leiden University, Leiden 2333CC, The Netherlands

2. Centre for Microbial Cell Biology, Leiden University, Leiden, The Netherlands

3. Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam 1098XH, The Netherlands

4. Animal Sciences, Institute of Biology Leiden, Leiden University, Leiden 2333CC, The Netherlands

5. Department of Human Genetics, Leiden University Medical Center, Leiden 2333ZC, The Netherlands

6. Biophysical Structural Chemistry, Leiden Institute of Chemistry, Leiden University, Leiden 2333CC, The Netherlands

7. Systems Biology, AMOLF Institute, Amsterdam 1098XG, The Netherlands

Abstract

Abstract The interplay between three-dimensional chromosome organisation and genomic processes such as replication and transcription necessitates in vivo studies of chromosome dynamics. Fluorescent organic dyes are often used for chromosome labelling in vivo. The mode of binding of these dyes to DNA cause its distortion, elongation, and partial unwinding. The structural changes induce DNA damage and interfere with the binding dynamics of chromatin-associated proteins, consequently perturbing gene expression, genome replication, and cell cycle progression. We have developed a minimally-perturbing, genetically encoded fluorescent DNA label consisting of a (photo-switchable) fluorescent protein fused to the DNA-binding domain of H-NS — a bacterial nucleoid-associated protein. We show that this DNA label, abbreviated as HI-NESS (H-NS-based indicator for nucleic acid stainings), is minimally-perturbing to genomic processes and labels chromosomes in eukaryotic cells in culture, and in zebrafish embryos with preferential binding to AT-rich chromatin.

Funder

Netherlands Organization for Scientific Research

Foundation for Fundamental Research on Matter

Human Frontier Science Program

Publisher

Oxford University Press (OUP)

Subject

Genetics

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