Literature DB >> 29605860

An Application-Directed, Versatile DNA FISH Platform for Research and Diagnostics.

Eleni Gelali1, Joaquin Custodio1, Gabriele Girelli1, Erik Wernersson1, Nicola Crosetto1, Magda Bienko2.   

Abstract

DNA fluorescence in situ hybridization (DNA FISH) has emerged as a powerful microscopy technique that allows a unique view into the composition and arrangement of the genetic material in its natural context-be it the cell nucleus in interphase, or chromosomes in metaphase spreads. The core principle of DNA FISH is the ability of fluorescently labeled DNA probes (either double- or single-stranded DNA fragments) to bind to their complementary sequences in situ in cells or tissues, revealing the location of their target as fluorescence signals detectable with a fluorescence microscope. Numerous variants and improvements of the original DNA FISH method as well as a vast repertoire of applications have been described since its inception more than 4 decades ago. In recent years, the development of many new fluorescent dyes together with drastic advancements in methods for probe generation (Boyle et al., Chromosome Res 19:901-909, 2011; Beliveau et al., Proc Natl Acad Sci U S A 109:21301-21306, 2012; Bienko et al., Nat Methods 10:122-124, 2012), as well as improvements in the resolution of microscopy technologies, have boosted the number of DNA FISH applications, particularly in the field of genome architecture (Markaki et al., Bioessays 34:412-426, 2012; Beliveau et al., Nat Commun 6:7147, 2015). However, despite these remarkable steps forward, choosing which type of DNA FISH sample preparation protocol, probe design, hybridization procedure, and detection method is best suited for a given application remains still challenging for many research labs, preventing a more widespread use of this powerful technology. Here, we present a comprehensive platform to help researchers choose which DNA FISH protocol is most suitable for their particular application. In addition, we describe computational pipelines that can be implemented for efficient DNA FISH probe design and for signal quantification. Our goal is to make DNA FISH a versatile and streamlined technique that can be easily implemented by both research and diagnostic labs.

Keywords:  Cytogenetics; DNA fluorescence in situ hybridization; Genome architecture; High-definition DNA FISH; Superresolution microscopy

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Year:  2018        PMID: 29605860     DOI: 10.1007/978-1-4939-7768-0_17

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  iFISH is a publically available resource enabling versatile DNA FISH to study genome architecture.

Authors:  Eleni Gelali; Gabriele Girelli; Masahiro Matsumoto; Erik Wernersson; Joaquin Custodio; Ana Mota; Maud Schweitzer; Katalin Ferenc; Xinge Li; Reza Mirzazadeh; Federico Agostini; John P Schell; Fredrik Lanner; Nicola Crosetto; Magda Bienko
Journal:  Nat Commun       Date:  2019-04-09       Impact factor: 14.919

Review 2.  Single-Cell RNA Sequencing (scRNA-seq) in Cardiac Tissue: Applications and Limitations.

Authors:  Mingqiang Wang; Mingxia Gu; Ling Liu; Yu Liu; Lei Tian
Journal:  Vasc Health Risk Manag       Date:  2021-10-02

3.  Simultaneous visualization of DNA loci in single cells by combinatorial multi-color iFISH.

Authors:  Ana Mota; Maud Schweitzer; Erik Wernersson; Nicola Crosetto; Magda Bienko
Journal:  Sci Data       Date:  2022-02-10       Impact factor: 6.444

  3 in total

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