Evidence map›Paper›PMID 32167469›Full record

ArticleeLife2020

Monoubiquitination by the human Fanconi anemia core complex clamps FANCI:FANCD2 on DNA in filamentous arrays.

Winnie Tan, Sylvie van Twest, Andrew Leis, Rohan Bythell-Douglas, Vincent J Murphy, Michael Sharp, Michael W Parker, Wayne Crismani, Andrew J Deans

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 78 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Winnie TanGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.ORCID 0000-0003-3229-4157
Sylvie van TwestGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.ORCID 0000-0001-5602-0906
Andrew LeisBio21 Institute, University of Melbourne, Parkville, Australia.ORCID 0000-0003-4905-9401
Rohan Bythell-DouglasGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.ORCID 0000-0002-3823-8749
Vincent J MurphyGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.
Michael SharpGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.ORCID 0000-0002-1019-3729
Michael W ParkerBio21 Institute, University of Melbourne, Parkville, Australia.ORCID 0000-0002-3101-1138
Wayne CrismaniGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.ORCID 0000-0003-0143-8293
Andrew J DeansGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Australia.ORCID 0000-0002-5271-4422
The University of Melbourne · AUSt Vincents Institute of Medical Research · AU

Funding

Maddie Riewoldt's Vision MRV2016Maddie Riewoldt's Vision SVI-MRV2017GNational Breast Cancer Foundation IIRS-19-017National Health and Medical Research Council GNT1117183National Health and Medical Research Council GNT1123100National Health and Medical Research Council GNT1123100 and GNT1181110National Health and Medical Research Council GNT1129757National Health and Medical Research Council GNT1156343National Health and Medical Research Council GNT1181110Victorian Government OIS Program
6 · The paper itself

Abstract

fanciFANCD2 monoubiquitination is a critical event for replication fork stabilization by the Fanconi anemia (FA) DNA repair pathway. It has been proposed that at stalled replication forks, monoubiquitinated-FANCD2 serves to recruit DNA repair proteins that contain ubiquitin-binding motifs. Here, we have reconstituted the FA pathway in vitro to study functional consequences of FANCI:FANCD2 monoubiquitination. We report that monoubiquitination does not promote any specific exogenous protein:protein interactions, but instead stabilizes FANCI:FANCD2 heterodimers on dsDNA. This clamping requires monoubiquitination of only the FANCD2 subunit. We further show using electron microscopy that purified monoubiquitinated FANCI:FANCD2 forms filament-like arrays on long dsDNA. Our results reveal how monoubiquitinated FANCI:FANCD2, defective in many cancer types and all cases of FA, is activated upon DNA binding.

Indexed as

DNA DamageDNA RepairDNA ReplicationFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group ProteinsHumansUbiquitinationFANCD2 protein, humanFANCI protein, humanFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group ProteinsbiochemistrychromosomesDNA repairFanconi anemiagene expressionhumanubiquitinxenopus

Identifiers

PMID32167469
PMCPMC7156235
OpenAlexW3011361504

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.