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Replication dynamics of recombination-dependent replication forks

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Replication dynamics of recombination-dependent replication forks. / Naiman, Karel; Campillo-Funollet, Eduard; Watson, Adam T. et al.
In: Nature Communications, Vol. 12, No. 1, 923, 10.02.2021.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Naiman, K, Campillo-Funollet, E, Watson, AT, Budden, A, Miyabe, I & Carr, AM 2021, 'Replication dynamics of recombination-dependent replication forks', Nature Communications, vol. 12, no. 1, 923. https://doi.org/10.1038/s41467-021-21198-0

APA

Naiman, K., Campillo-Funollet, E., Watson, A. T., Budden, A., Miyabe, I., & Carr, A. M. (2021). Replication dynamics of recombination-dependent replication forks. Nature Communications, 12(1), Article 923. https://doi.org/10.1038/s41467-021-21198-0

Vancouver

Naiman K, Campillo-Funollet E, Watson AT, Budden A, Miyabe I, Carr AM. Replication dynamics of recombination-dependent replication forks. Nature Communications. 2021 Feb 10;12(1):923. doi: 10.1038/s41467-021-21198-0

Author

Naiman, Karel ; Campillo-Funollet, Eduard ; Watson, Adam T. et al. / Replication dynamics of recombination-dependent replication forks. In: Nature Communications. 2021 ; Vol. 12, No. 1.

Bibtex

@article{3bb8513f5b054e058ff8dddddf425e93,
title = "Replication dynamics of recombination-dependent replication forks",
abstract = "Replication forks restarted by homologous recombination are error prone and replicate both strands semi-conservatively using Pol δ. Here, we use polymerase usage sequencing to visualize in vivo replication dynamics of HR-restarted forks at an S. pombe replication barrier, RTS1, and model replication by Monte Carlo simulation. We show that HR-restarted forks synthesise both strands with Pol δ for up to 30 kb without maturing to a δ/ε configuration and that Pol α is not used significantly on either strand, suggesting the lagging strand template remains as a gap that is filled in by Pol δ later. We further demonstrate that HR-restarted forks progress uninterrupted through a fork barrier that arrests canonical forks. Finally, by manipulating lagging strand resection during HR-restart by deleting pku70, we show that the leading strand initiates replication at the same position, signifying the stability of the 3' single strand in the context of increased resection.",
author = "Karel Naiman and Eduard Campillo-Funollet and Watson, {Adam T.} and Alice Budden and Izumi Miyabe and Carr, {Antony M.}",
year = "2021",
month = feb,
day = "10",
doi = "10.1038/s41467-021-21198-0",
language = "English",
volume = "12",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "Nature Publishing Group",
number = "1",

}

RIS

TY - JOUR

T1 - Replication dynamics of recombination-dependent replication forks

AU - Naiman, Karel

AU - Campillo-Funollet, Eduard

AU - Watson, Adam T.

AU - Budden, Alice

AU - Miyabe, Izumi

AU - Carr, Antony M.

PY - 2021/2/10

Y1 - 2021/2/10

N2 - Replication forks restarted by homologous recombination are error prone and replicate both strands semi-conservatively using Pol δ. Here, we use polymerase usage sequencing to visualize in vivo replication dynamics of HR-restarted forks at an S. pombe replication barrier, RTS1, and model replication by Monte Carlo simulation. We show that HR-restarted forks synthesise both strands with Pol δ for up to 30 kb without maturing to a δ/ε configuration and that Pol α is not used significantly on either strand, suggesting the lagging strand template remains as a gap that is filled in by Pol δ later. We further demonstrate that HR-restarted forks progress uninterrupted through a fork barrier that arrests canonical forks. Finally, by manipulating lagging strand resection during HR-restart by deleting pku70, we show that the leading strand initiates replication at the same position, signifying the stability of the 3' single strand in the context of increased resection.

AB - Replication forks restarted by homologous recombination are error prone and replicate both strands semi-conservatively using Pol δ. Here, we use polymerase usage sequencing to visualize in vivo replication dynamics of HR-restarted forks at an S. pombe replication barrier, RTS1, and model replication by Monte Carlo simulation. We show that HR-restarted forks synthesise both strands with Pol δ for up to 30 kb without maturing to a δ/ε configuration and that Pol α is not used significantly on either strand, suggesting the lagging strand template remains as a gap that is filled in by Pol δ later. We further demonstrate that HR-restarted forks progress uninterrupted through a fork barrier that arrests canonical forks. Finally, by manipulating lagging strand resection during HR-restart by deleting pku70, we show that the leading strand initiates replication at the same position, signifying the stability of the 3' single strand in the context of increased resection.

U2 - 10.1038/s41467-021-21198-0

DO - 10.1038/s41467-021-21198-0

M3 - Journal article

C2 - 33568651

VL - 12

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

IS - 1

M1 - 923

ER -