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HI-NESS: a family of genetically encoded DNA labels based on a bacterial nucleoid-associated protein
Author(s) -
FatemaZahra M. Rashid,
Eike K. Mahlandt,
Michiel van der Vaart,
Daphne E.C. Boer,
Mónica Varela,
Bram Henneman,
Daan J.W. Brocken,
Patrick Voskamp,
Anneloes Blok,
Thomas Shimizu,
Annemarie H. Meijer,
Martijn S. Luijsterburg,
Joachim Goedhart,
Frédéric Crémazy,
Remus T. Dame
Publication year - 2021
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkab993
Subject(s) - biology , chromatin , dna , nucleoid , dna replication , microbiology and biotechnology , circular bacterial chromosome , control of chromosome duplication , dna binding protein , genetics , seqa protein domain , gene , transcription factor , escherichia coli
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.

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