Počet záznamů: 1  

Image analysis workflows to reveal the spatial organization of cell nuclei and chromosomes

  1. 1.
    SYSNO ASEP0566546
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevImage analysis workflows to reveal the spatial organization of cell nuclei and chromosomes
    Tvůrce(i) Randall, R. S. (CH)
    Jourdain, C. (DE)
    Nowicka, Anna (UEB-Q) ORCID
    Kaduchová, Kateřina (UEB-Q) ORCID
    Kubová, M. (CZ)
    Ayoub, M. A. (DE)
    Schubert, V. (DE)
    Tatout, C. (FR)
    Colas, I. (FR)
    Kalyanikrishna, A. (DE)
    Desset, S. (FR)
    Mermet, S. (FR)
    Boulaflous-Stevens, A. (FR)
    Kubalová, I. (CZ)
    Mandáková, T. (CZ)
    Heckmann, S. (DE)
    Lysák, M. A. (CZ)
    Panatta, M. (CH)
    Santoro, R. (DE)
    Schubert, D. (DE)
    Pečinka, Aleš (UEB-Q) ORCID, RID
    Routh, D. (CH)
    Baroux, C. (CH)
    Celkový počet autorů23
    Zdroj.dok.Nucleus. - : Taylor & Francis - ISSN 1949-1034
    Roč. 13, č. 1 (2022), s. 277-299
    Poč.str.23 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slova3D organization ; chromatin ; chromosome ; crossovers ; image analysis ; meiosis ; metaphase ; mitosis ; nuclear bodies ; nuclear speckles ; Nucleus ; oligo FISH ; pachytene ; quantification ; RNA Pol II ; segmentation ; sim ; spatial distribution ; STED imaging ; transcription factories
    Obor OECDCell biology
    CEPEF16_019/0000827 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    LM2018129 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    GA21-02929S GA ČR - Grantová agentura ČR
    Způsob publikováníOpen access
    Institucionální podporaUEB-Q - RVO:61389030
    UT WOS000898422400001
    EID SCOPUS85143064143
    DOI10.1080/19491034.2022.2144013
    AnotaceNucleus, chromatin, and chromosome organization studies heavily rely on fluorescence microscopy imaging to elucidate the distribution and abundance of structural and regulatory components. Three-dimensional (3D) image stacks are a source of quantitative data on signal intensity level and distribution and on the type and shape of distribution patterns in space. Their analysis can lead to novel insights that are otherwise missed in qualitative-only analyses. Quantitative image analysis requires specific software and workflows for image rendering, processing, segmentation, setting measurement points and reference frames and exporting target data before further numerical processing and plotting. These tasks often call for the development of customized computational scripts and require an expertise that is not broadly available to the community of experimental biologists. Yet, the increasing accessibility of high- and super-resolution imaging methods fuels the demand for user-friendly image analysis workflows. Here, we provide a compendium of strategies developed by participants of a training school from the COST action INDEPTH to analyze the spatial distribution of nuclear and chromosomal signals from 3D image stacks, acquired by diffraction-limited confocal microscopy and super-resolution microscopy methods (SIM and STED). While the examples make use of one specific commercial software package, the workflows can easily be adapted to concurrent commercial and open-source software. The aim is to encourage biologists lacking custom-script-based expertise to venture into quantitative image analysis and to better exploit the discovery potential of their images. Abbreviations: 3D FISH: three-dimensional fluorescence in situ hybridization, 3D: three-dimensional, ASY1: ASYNAPTIC 1, CC: chromocenters, CO: Crossover, DAPI: 4',6-diamidino-2-phenylindole, DMC1: DNA MEIOTIC RECOMBINASE 1, DSB: Double-Strand Break, FISH: fluorescence in situ hybridization, GFP: GREEN FLUORESCENT PROTEIN, HEI10: HUMAN ENHANCER OF INVASION 10, NCO: Non-Crossover, NE: Nuclear Envelope, Oligo-FISH: oligonucleotide fluorescence in situ hybridization, RNPII: RNA Polymerase II, SC: Synaptonemal Complex, SIM: structured illumination microscopy, ZMM (ZIP: MSH4: MSH5 and MER3 proteins), ZYP1: ZIPPER-LIKE PROTEIN 1.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2023
    Elektronická adresahttps://doi.org/10.1080/19491034.2022.2144013
Počet záznamů: 1  

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