Evidence map›Paper›PMID 30082684›Full record

ArticleNature communications2018

AND-1 fork protection function prevents fork resection and is essential for proliferation.

Takuya Abe, Ryotaro Kawasumi, Michele Giannattasio, Sabrina Dusi, Yui Yoshimoto, Keiji Miyata, Koyuki Umemura, Kouji Hirota, Dana Branzei

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed.

  1. Article
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  7. Review
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  9. Article
  10. Review
  11. Article
  12. RAD52 prevents accumulation ofbioRxiv : the preprint server for biology · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. The TIMELESS effort for timely DNA replication and protection.Cellular and molecular life sciences : CMLS · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Takuya AbeIFOM, the FIRC Institute of Molecular Oncology, Via Adamello 16, 20139, Milan, Italy.
Ryotaro KawasumiIFOM, the FIRC Institute of Molecular Oncology, Via Adamello 16, 20139, Milan, Italy.ORCID http://orcid.org/0000-0002-6527-6329
Michele GiannattasioIFOM, the FIRC Institute of Molecular Oncology, Via Adamello 16, 20139, Milan, Italy.ORCID http://orcid.org/0000-0001-7099-5718
Sabrina DusiIFOM, the FIRC Institute of Molecular Oncology, Via Adamello 16, 20139, Milan, Italy.
Yui YoshimotoDepartment of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Minamiosawa 1-1, Hachioji-shi, Tokyo, 192-0397, Japan.
Keiji MiyataDepartment of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Minamiosawa 1-1, Hachioji-shi, Tokyo, 192-0397, Japan.
Koyuki UmemuraDepartment of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Minamiosawa 1-1, Hachioji-shi, Tokyo, 192-0397, Japan.
Kouji HirotaDepartment of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Minamiosawa 1-1, Hachioji-shi, Tokyo, 192-0397, Japan.ORCID http://orcid.org/0000-0003-1676-979X
Dana BranzeiIFOM, the FIRC Institute of Molecular Oncology, Via Adamello 16, 20139, Milan, Italy. dana.branzei@ifom.eu.

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) IG 14171Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) IG 18976EC | European Research Council (ERC) 242928EC | European Research Council (ERC) 682190European Research Council 242928
6 · The paper itself

Abstract

AND-1/Ctf4 bridges the CMG helicase and DNA polymerase alpha, facilitating replication. Using an inducible degron system in avian cells, we find that AND-1 depletion is incompatible with proliferation, owing to cells accumulating in G2 with activated DNA damage checkpoint. Replication without AND-1 causes fork speed slow-down and accumulation of long single-stranded DNA (ssDNA) gaps at the replication fork junction, with these regions being converted to DNA double strand breaks (DSBs) in G2. Strikingly, resected forks and DNA damage accumulation in G2, but not fork slow-down, are reverted by treatment with mirin, an MRE11 nuclease inhibitor. Domain analysis of AND-1 further revealed that the HMG box is important for fast replication but not for proliferation, whereas conversely, the WD40 domain prevents fork resection and subsequent DSB-associated lethality. Thus, our findings uncover a fork protection function of AND-1/Ctf4 manifested via the WD40 domain that is essential for proliferation and averts genome instability.

Indexed as

Cell ProliferationDNA ReplicationGene Expression RegulationAnimalsChickensDNA-Binding ProteinsDNA Breaks, Double-StrandedDNA Polymerase IDNA RepairDNA, Single-StrandedG2 PhaseHistonesHumansMutationProtein BindingProtein DomainsDNA-Binding ProteinsDNA Polymerase IDNA, Single-StrandedH2AX protein, humanHistonesWDHD1 protein, human

Identifiers

PMID30082684
PMCPMC6079002

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.