Evidence map›Paper›PMID 23388460›Full record

ArticleCell cycle (Georgetown, Tex.)2013

Recruitment of DNA polymerase eta by FANCD2 in the early response to DNA damage.

Dechen Fu, Fred Duafalia Dudimah, Jun Zhang, Anna Pickering, Jayabal Paneerselvam, Manikandan Palrasu, Hong Wang, Peiwen Fei

Open access · hybridAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

42 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Focal Point of Fanconi Anemia Signaling.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Multifaceted Fanconi Anemia Signaling.Trends in genetics : TIG · 2018
    Review
  15. Fanconi Anemia Signaling and Cancer.Trends in cancer · 2017
    Review
  16. Article
  17. FANCD2 and DNA Damage.International journal of molecular sciences · 2017
    Review
  18. Article
  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

8 authors at 5 institutions in 1 country.

Dechen FuUniversity of Hawaii Cancer Center (UHCC), University of Hawaii, Honolulu, HI, USA.
Fred Duafalia Dudimah
Jun Zhang
Anna Pickering
Jayabal Paneerselvam
Manikandan Palrasu
Hong Wang
Peiwen Fei
University of Hawaii Cancer CenterUniversity of Hawaiʻi at Mānoa · USCancer Center of Hawaii · USMayo Clinic · USUniversity of Minnesota Rochester · US

Funding

Roles of the Fanconi Anemia Pathway in Bladder TumorigenesisR01CA136532 · NCI · UNIVERSITY OF MINNESOTA · PI FEI, PEIWEN · 2009 to 2013
$1.5M
NCI NIH HHS R01 CA136532PHS HHS CAR01CA136532
6 · The paper itself

Abstract

How Fanconi anemia (FA) protein D2 (FANCD2) performs DNA damage repair remains largely elusive. We report here that translesion synthesis DNA polymerase (pol) eta is a novel mediator of FANCD2 function. We found that wild type (wt) FANCD2, not K561R (mt) FANCD2, can interact with pol eta. Upon DNA damage, the interaction of pol eta with FANCD2 occurs earlier than that with PCNA, which is in concert with our finding that FANCD2 monoubiquitination peaks at an earlier time point than that of PCNA monoubiquitination. FANCD2-null FA patient cells (PD20) carrying histone H2B-fused pol eta and wtFANCD2, respectively, show a similar tendency of low Mitomycin C (MMC) sensitivity, while cells transfected with empty vector control or pol eta alone demonstrate a similar high level of MMC sensitivity. It therefore appears that FANCD2 monoubiquitination plays a similar anchor role as histone to bind DNA in regulating pol eta. Collectively, our study indicates that, in the early phase of DNA damage response, FANCD2 plays crucial roles in recruiting pol eta to the sites of DNA damage for repair.

Indexed as

DNA DamageCell LineChromatinDNA-Directed DNA PolymeraseFanconi Anemia Complementation Group D2 ProteinHeLa CellsHistonesHumansMitomycinModels, BiologicalMultiprotein ComplexesMutationProliferating Cell Nuclear AntigenProtein BindingProtein Structure, TertiaryUbiquitinated ProteinsChromatinDNA-Directed DNA PolymeraseFANCD2 protein, humanFanconi Anemia Complementation Group D2 ProteinHistonesMitomycinMultiprotein ComplexesProliferating Cell Nuclear AntigenRad30 proteinUbiquitinated ProteinsY-Family DNA Polymerasescancer susceptibility syndromeDNA polymerase etaearly DNA damage responseerror-free TLFANCD2genome stabilityPCNAthe FA tumor suppressor pathwaytranslesion synthesisXP-V

Identifiers

PMID23388460
PMCPMC3610727
OpenAlexW2023489614

What OpenQuestion holds

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Registered trials

None linked

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.