IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v15y2024i1d10.1038_s41467-024-50047-z.html
   My bibliography  Save this article

The Escherichia coli chromosome moves to the replisome

Author

Listed:
  • Konrad Gras

    (Uppsala University)

  • David Fange

    (Uppsala University)

  • Johan Elf

    (Uppsala University)

Abstract

In Escherichia coli, it is debated whether the two replisomes move independently along the two chromosome arms during replication or if they remain spatially confined. Here, we use high-throughput fluorescence microscopy to simultaneously determine the location and short-time-scale (1 s) movement of the replisome and a chromosomal locus throughout the cell cycle. The assay is performed for several loci. We find that (i) the two replisomes are confined to a region of ~250 nm and ~120 nm along the cell’s long and short axis, respectively, (ii) the chromosomal loci move to and through this region sequentially based on their distance from the origin of replication, and (iii) when a locus is being replicated, its short time-scale movement slows down. This behavior is the same at different growth rates. In conclusion, our data supports a model with DNA moving towards spatially confined replisomes at replication.

Suggested Citation

  • Konrad Gras & David Fange & Johan Elf, 2024. "The Escherichia coli chromosome moves to the replisome," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-50047-z
    DOI: 10.1038/s41467-024-50047-z
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-50047-z
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-50047-z?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Sarah M Mangiameli & Brian T Veit & Houra Merrikh & Paul A Wiggins, 2017. "The Replisomes Remain Spatially Proximal throughout the Cell Cycle in Bacteria," PLOS Genetics, Public Library of Science, vol. 13(1), pages 1-17, January.
    2. M. Charl Moolman & Sriram Tiruvadi Krishnan & Jacob W. J. Kerssemakers & Aafke van den Berg & Pawel Tulinski & Martin Depken & Rodrigo Reyes-Lamothe & David J. Sherratt & Nynke H. Dekker, 2014. "Slow unloading leads to DNA-bound β2-sliding clamp accumulation in live Escherichia coli cells," Nature Communications, Nature, vol. 5(1), pages 1-11, December.
    3. Martin Lindén & Vladimir Ćurić & Elias Amselem & Johan Elf, 2017. "Pointwise error estimates in localization microscopy," Nature Communications, Nature, vol. 8(1), pages 1-9, August.
    4. Aleksandre Japaridze & Christos Gogou & Jacob W. J. Kerssemakers & Huyen My Nguyen & Cees Dekker, 2020. "Direct observation of independently moving replisomes in Escherichia coli," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
    5. Avelino Javer & Zhicheng Long & Eileen Nugent & Marco Grisi & Kamin Siriwatwetchakul & Kevin D. Dorfman & Pietro Cicuta & Marco Cosentino Lagomarsino, 2013. "Short-time movement of E. coli chromosomal loci depends on coordinate and subcellular localization," Nature Communications, Nature, vol. 4(1), pages 1-8, October.
    6. Ismath Sadhir & Seán M. Murray, 2023. "Mid-cell migration of the chromosomal terminus is coupled to origin segregation in Escherichia coli," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Chen Zhang & Asha Mary Joseph & Laurent Casini & Justine Collier & Anjana Badrinarayanan & Suliana Manley, 2024. "Chromosome organization shapes replisome dynamics in Caulobacter crescentus," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    2. Janni Harju & Muriel C. F. Teeseling & Chase P. Broedersz, 2024. "Loop-extruders alter bacterial chromosome topology to direct entropic forces for segregation," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    3. Mikhail Metelev & Erik Lundin & Ivan L. Volkov & Arvid H. Gynnå & Johan Elf & Magnus Johansson, 2022. "Direct measurements of mRNA translation kinetics in living cells," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    4. Mareike Berger & Pieter Rein ten Wolde, 2022. "Robust replication initiation from coupled homeostatic mechanisms," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    5. Elena Espinosa & Jihane Challita & Jean-Michel Desfontaines & Christophe Possoz & Marie-Eve Val & Didier Mazel & Martial Marbouty & Romain Koszul & Elisa Galli & François-Xavier Barre, 2024. "MatP local enrichment delays segregation independently of tetramer formation and septal anchoring in Vibrio cholerae," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    6. David Geisel & Peter Lenz, 2022. "Machine learning classification of trajectories from molecular dynamics simulations of chromosome segregation," PLOS ONE, Public Library of Science, vol. 17(1), pages 1-33, January.
    7. Miloš Tišma & Florian Patrick Bock & Jacob Kerssemakers & Hammam Antar & Aleksandre Japaridze & Stephan Gruber & Cees Dekker, 2024. "Direct observation of a crescent-shape chromosome in expanded Bacillus subtilis cells," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    8. Ofir Shukron & David Holcman, 2017. "Transient chromatin properties revealed by polymer models and stochastic simulations constructed from Chromosomal Capture data," PLOS Computational Biology, Public Library of Science, vol. 13(4), pages 1-20, April.
    9. Agathe Couturier & Chloé Virolle & Kelly Goldlust & Annick Berne-Dedieu & Audrey Reuter & Sophie Nolivos & Yoshiharu Yamaichi & Sarah Bigot & Christian Lesterlin, 2023. "Real-time visualisation of the intracellular dynamics of conjugative plasmid transfer," Nature Communications, Nature, vol. 14(1), pages 1-15, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-50047-z. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.