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Mitochondrial Nucleoids: Superresolution microscopy analysis

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    SYSNO ASEP0504242
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMitochondrial Nucleoids: Superresolution microscopy analysis
    Author(s) Ježek, Petr (FGU-C) RID, ORCID
    Špaček, Tomáš (FGU-C) RID, ORCID
    Tauber, Jan (FGU-C) RID, ORCID
    Pavluch, Vojtěch (FGU-C) RID, ORCID
    Source TitleInternational Journal of Biochemistry and Cell Biology. - : Elsevier - ISSN 1357-2725
    Roč. 106, Jan (2019), s. 21-25
    Number of pages5 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsmtDNA ; nucleoids ; 3D superresolution microscopy ; TFAM
    Subject RIVEA - Cell Biology
    OECD categoryCell biology
    R&D ProjectsGA16-04788S GA ČR - Czech Science Foundation (CSF)
    GA17-01813S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportFGU-C - RVO:67985823
    UT WOS000456221500003
    EID SCOPUS85056466270
    DOI10.1016/j.biocel.2018.10.012
    AnnotationThe mitochondrion owns an autonomous genome. Double-stranded circular mitochondrial DNA (mtDNA) is organized in complexes with a packing/stabilizing transcription factor TFAM, having multiple roles, and proteins of gene expression machinery in structures called nucleoids. From hundreds to thousands nucleoids exist distributed in the matrix of mitochondria] reticulum network. A single mtDNA molecule contained within the single nucleoid is a currently preferred but questioned model. Nevertheless, mtDNA replication should lead transiently to its doubling within a nucleoid. However, nucleoid division has not yet been documented in detail. A 3D superresolution microscopy is required to resolve nucleoid biology occurring in similar to 100 nm space, having an advantage over electron microscopy tomography in resolving the particular protein components. We discuss stochastic vs. stimulated emission depletion microscopy yielding wide vs. narrow nucleoid size distribution, respectively. Nucleoid clustering into spheroids fragmented from the continuous mitochondria] network, likewise possible nucleoid attachment to the inner membrane is reviewed.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2020
    Electronic addresshttps://doi.org/10.1016/j.biocel.2018.10.012
Number of the records: 1  

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