Evidence map›Paper›PMID 21896657›Full record

ArticleGenes & development2011

Regulation of the Fanconi anemia pathway by a SUMO-like delivery network.

Kailin Yang, George-Lucian Moldovan, Patrizia Vinciguerra, Junko Murai, Shunichi Takeda, Alan D D'Andrea

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing 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

71 citing papers in PubMed, 116 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. ATAD5 functions as a regulatory platform for Ub-PCNA deubiquitination.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. SUMO and the DNA damage response.Biochemical Society transactions · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Structural basis of FANCD2 deubiquitination by USP1-UAF1.Nature structural & molecular biology · 2021
    Article
  17. Molecular Mechanisms of DUBs Regulation in Signaling and Disease.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Kailin YangDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA;
George-Lucian Moldovan
Patrizia Vinciguerra
Junko Murai
Shunichi Takeda
Alan D D'Andrea
Dana-Farber Cancer Institute · USKyoto University · JP

Funding

Transcription-Coupled & Replication-Associated Excision RepairP01CA092584 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI John A. Tainer · 2001 to 2026
$89.6M
MOLECULAR PATHOGENESIS OF FANCONI ANEMIAR01HL052725 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI ALAN D. D'ANDREA · 1994 to 2026
$5.9M
STRUCTURE AND FUNCTION OF THE ERYTHROPOIETIN RECEPTORR01DK043889 · NIDDK · DANA-FARBER CANCER INSTITUTE · PI D'ANDREA, ALAN D. · 1992 to 2014
$5.3M
NCI NIH HHS P01 CA092584NCI NIH HHS P01CA092584NHLBI NIH HHS R01 HL052725NHLBI NIH HHS R01HL52725NIDDK NIH HHS R01 DK043889NIDDK NIH HHS R01DK43889
6 · The paper itself

Abstract

The USP1/UAF1 complex deubiquitinates the Fanconi anemia protein FANCD2, thereby promoting homologous recombination and DNA cross-link repair. How USP1/UAF1 is targeted to the FANCD2/FANCI heterodimer has remained unknown. Here we show that UAF1 contains a tandem repeat of SUMO-like domains in its C terminus (SLD1 and SLD2). SLD2 binds directly to a SUMO-like domain-interacting motif (SIM) on FANCI. Deletion of the SLD2 sequence of UAF1 or mutation of the SIM on FANCI disrupts UAF1/FANCI binding and inhibits FANCD2 deubiquitination and DNA repair. The USP1/UAF1 complex also deubiquitinates PCNA-Ub, and deubiquitination requires the PCNA-binding protein hELG1. The SLD2 sequence of UAF1 binds to a SIM on hELG1, thus targeting the USP1/UAF1 complex to its PCNA-Ub substrate. We propose that the regulated targeting of USP1/UAF1 to its DNA repair substrates, FANCD2-Ub and PCNA-Ub, by SLD-SIM interactions coordinates homologous recombination and translesion DNA synthesis.

Indexed as

Gene Expression RegulationAdenosine TriphosphatasesAmino Acid SequenceAnimalsArabidopsis ProteinsATPases Associated with Diverse Cellular ActivitiesCell LineChickensDNA-Binding ProteinsEndopeptidasesFanconi Anemia Complementation Group ProteinsGene Knockdown TechniquesHeLa CellsHumansModels, MolecularNuclear ProteinsAdenosine TriphosphatasesArabidopsis ProteinsATAD5 protein, humanATPases Associated with Diverse Cellular ActivitiesDNA-Binding ProteinsEndopeptidasesFanconi Anemia Complementation Group ProteinsNuclear ProteinsProliferating Cell Nuclear AntigenSmall Ubiquitin-Related Modifier ProteinsUbiquitinUbiquitin-Specific ProteasesUSP1 protein, humanWDR48 protein, human

Identifiers

PMID21896657
PMCPMC3175720
OpenAlexW2112158920

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.