Evidence map›Paper›PMID 29030393›Full record

ArticleThe Journal of cell biology2017

Fanconi anemia FANCD2 and FANCI proteins regulate the nuclear dynamics of splicing factors.

María Moriel-Carretero, Sara Ovejero, Marie Gérus-Durand, Dimos Vryzas, Angelos Constantinou

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Observational
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  4. Article
  5. Review
  6. Article
  7. Focal Point of Fanconi Anemia Signaling.International journal of molecular sciences · 2021
    Review
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  10. Article
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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

5 authors at 1 institution in 1 country.

María Moriel-CarreteroInstitute of Human Genetics, Centre National de la Recherche Scientifique UMR 9002, Université de Montpellier, Montpellier, France.ORCID 0000-0002-6770-3486
Sara OvejeroInstitute of Human Genetics, Centre National de la Recherche Scientifique UMR 9002, Université de Montpellier, Montpellier, France.ORCID 0000-0002-8354-856X
Marie Gérus-DurandInstitute of Human Genetics, Centre National de la Recherche Scientifique UMR 9002, Université de Montpellier, Montpellier, France.ORCID 0000-0002-4377-9857
Dimos VryzasInstitute of Human Genetics, Centre National de la Recherche Scientifique UMR 9002, Université de Montpellier, Montpellier, France.ORCID 0000-0001-5925-6658
Angelos ConstantinouInstitute of Human Genetics, Centre National de la Recherche Scientifique UMR 9002, Université de Montpellier, Montpellier, France angelos.constantinou@igh.cnrs.fr.ORCID 0000-0002-2994-8140
Université de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteins disabled in the cancer-prone disorder Fanconi anemia (FA) ensure the maintenance of chromosomal stability during DNA replication. FA proteins regulate replication dynamics, coordinate replication-coupled repair of interstrand DNA cross-links, and mitigate conflicts between replication and transcription. Here we show that FANCI and FANCD2 associate with splicing factor 3B1 (SF3B1), a key spliceosomal protein of the U2 small nuclear ribonucleoprotein (U2 snRNP). FANCI is in close proximity to SF3B1 in the nucleoplasm of interphase and mitotic cells. Furthermore, we find that DNA replication stress induces the release of SF3B1 from nuclear speckles in a manner that depends on FANCI and on the activity of the checkpoint kinase ATR. In chromatin, both FANCD2 and FANCI associate with SF3B1, prevent accumulation of postcatalytic intron lariats, and contribute to the timely eviction of splicing factors. We propose that FANCD2 and FANCI contribute to the organization of functional domains in chromatin, ensuring the coordination of DNA replication and cotranscriptional processes.

Indexed as

DNA ReplicationTranscription, GeneticAtaxia Telangiectasia Mutated ProteinsCell Line, TumorChromatinFanconi AnemiaFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group ProteinsFibroblastsGenes, ReporterHEK293 CellsHeLa CellsHumansMitosisOligopeptidesOsteoblastsAtaxia Telangiectasia Mutated ProteinsATR protein, humanChromatinFANCD2 protein, humanFANCI protein, humanFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group ProteinsFLAG peptideOligopeptidesPhosphoproteinsRibonucleoprotein, U2 Small NuclearRNA Splicing FactorsSF3B1 protein, human

Identifiers

PMID29030393
PMCPMC5716273
OpenAlexW2761488822

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.