4.7 Article

Direct monitoring of the stepwise condensation of kinetoplast DNA networks

Journal

SCIENTIFIC REPORTS
Volume 11, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-81045-6

Keywords

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Funding

  1. United States-Israel Binational Science Foundation, Jerusalem, Israel [2011156]
  2. Israel Science Foundation [1127/10, 1021/14]
  3. Minerva Center for Bio-Hybrid complex systems

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This study focused on the condensation of kinetoplast DNA (kDNA), the mitochondrial genome of kinetoplastids, and revealed the role of the replication protein UMSBP in decondensation and initiation of kDNA replication. The condensation of kDNA was found to proceed through a series of hierarchical steps, with multiple local condensation foci assembling into higher order condensation centers, influenced by the maxicircles component of kDNA. The structure of condensing kDNA intermediates shed light on the organization of the condensed kDNA network within the mitochondrial nucleoid.
Condensation and remodeling of nuclear genomes play an essential role in the regulation of gene expression and replication. Yet, our understanding of these processes and their regulatory role in other DNA-containing organelles, has been limited. This study focuses on the packaging of kinetoplast DNA (kDNA), the mitochondrial genome of kinetoplastids. Severe tropical diseases, affecting large human populations and livestock, are caused by pathogenic species of this group of protists. kDNA consists of several thousand DNA minicircles and several dozen DNA maxicircles that are linked topologically into a remarkable DNA network, which is condensed into a mitochondrial nucleoid. In vitro analyses implicated the replication protein UMSBP in the decondensation of kDNA, which enables the initiation of kDNA replication. Here, we monitored the condensation of kDNA, using fluorescence and atomic force microscopy. Analysis of condensation intermediates revealed that kDNA condensation proceeds via sequential hierarchical steps, where multiple interconnected local condensation foci are generated and further assemble into higher order condensation centers, leading to complete condensation of the network. This process is also affected by the maxicircles component of kDNA. The structure of condensing kDNA intermediates sheds light on the structural organization of the condensed kDNA network within the mitochondrial nucleoid.

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