Evidence map›Paper›PMID 20347429›Full record

ArticleMolecular cell2010

MHF1-MHF2, a histone-fold-containing protein complex, participates in the Fanconi anemia pathway via FANCM.

Thiyam Ramsing Singh, Dorina Saro, Abdullah Mahmood Ali, Xiao-Feng Zheng, Chang-hu Du, Michael W Killen, Aristidis Sachpatzidis, Kebola Wahengbam, Andrew J Pierce, Yong Xiong and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

129 citing papers in PubMed, 195 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Recent advances in plant kinetochore research.Frontiers in cell and developmental biology · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Biochemical and crystallization analysis of the CENP-SX-DNA complex.Acta crystallographica. Section F, Structural biology communications · 2022
    Article
  12. Review
  13. Type-I Interferon Signaling in Fanconi Anemia.Frontiers in cellular and infection microbiology · 2022
    Review
  14. Kinetochore Architecture Employs Diverse Linker Strategies Across Evolution.Frontiers in cell and developmental biology · 2022
    Review
  15. Article
  16. Review
  17. Article
  18. Structural analysis of the chicken FANCM-MHF complex and its stability.Acta crystallographica. Section F, Structural biology communications · 2021
    Article
  19. Article
  20. Review

69 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Thiyam Ramsing SinghDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
Dorina Saro
Abdullah Mahmood Ali
Xiao-Feng Zheng
Chang-hu Du
Michael W Killen
Aristidis Sachpatzidis
Kebola Wahengbam
Andrew J Pierce
Yong Xiong
Patrick Sung
Amom Ruhikanta Meetei
Cincinnati Children's Hospital Medical Center · USYale University · USUniversity of Kentucky · US

Funding

YEAST DNA REPAIR GENES AND PROTEINS OF THE RAD52 GROUPR01ES007061 · NIEHS · YALE UNIVERSITY · PI Patrick Sung · 1995 to 2026
$9.4M
Roles of the RecQ Helicases BLM and RECQ5 in Genome MaintenanceR01ES015632 · NIEHS · YALE UNIVERSITY · PI SUNG, PATRICK · 2007 to 2017
$3.9M
Function and Regulation of FANCM in Fanconi AnemiaR01HL084082 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI MEETEI, RUHIKANTA AMOM · 2007 to 2011
$2.1M
NHLBI NIH HHS HL084082NHLBI NIH HHS R01 HL084082NIEHS NIH HHS ES015632NIEHS NIH HHS ES07061NIEHS NIH HHS R01 ES007061NIEHS NIH HHS R01 ES015632
6 · The paper itself

Abstract

FANCM is a Fanconi anemia nuclear core complex protein required for the functional integrity of the FANC-BRCA pathway of DNA damage response and repair. Here we report the isolation and characterization of two histone-fold-containing FANCM-associated proteins, MHF1 and MHF2. We show that suppression of MHF1 expression results in (1) destabilization of FANCM and MHF2, (2) impairment of DNA damage-induced monoubiquitination and foci formation of FANCD2, (3) defective chromatin localization of FA nuclear core complex proteins, (4) elevated MMC-induced chromosome aberrations, and (5) sensitivity to MMC and camptothecin. We also provide biochemical evidence that MHF1 and MHF2 assemble into a heterodimer that binds DNA and enhances the DNA branch migration activity of FANCM. These findings reveal critical roles of the MHF1-MHF2 dimer in DNA damage repair and genome maintenance through FANCM.

Indexed as

Protein FoldingProtein MultimerizationCell Line, TumorDNADNA-Binding ProteinsDNA HelicasesFanconi AnemiaHistonesHumansProtein BindingDNADNA-Binding ProteinsDNA HelicasesFANCM protein, humanHistones

Identifiers

PMID20347429
PMCPMC2848122
OpenAlexW1965495050

What OpenQuestion holds

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Read underepoch 390

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.