Evidence map›Paper›PMID 34819671›Full record

ArticleNature2021

Fam72a enforces error-prone DNA repair during antibody diversification.

Mélanie Rogier, Jacques Moritz, Isabelle Robert, Chloé Lescale, Vincent Heyer, Arthur Abello, Ophélie Martin, Katia Capitani, Morgane Thomas, Anne-Sophie Thomas-Claudepierre and 9 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 56 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

19 authors at 5 institutions in 3 countries.

Mélanie Rogier *Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.ORCID http://orcid.org/0000-0002-0522-8931
Jacques Moritz *Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.
Isabelle RobertInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.ORCID http://orcid.org/0000-0001-6533-8297
Chloé LescaleGenome Integrity, Immunity and Cancer Unit, Equipe Labellisée Ligue Contre Le Cancer, INSERM U1223, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0003-0622-1149
Vincent HeyerInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.
Arthur AbelloInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.
Ophélie MartinGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, UK.
Katia CapitaniCore Research Laboratory, ISPRO, Firenze, Italy.
Morgane ThomasCentre National de la Recherche Scientifique (CNRS), UMR7276, Institut National de la Santé et de la Recherche Médicale (INSERM), UMR1262-Contrôle de la Réponse Immune B et Lymphoproliférations, Université de Limoges, Limoges, France.
Anne-Sophie Thomas-ClaudepierreInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.
Brice LaffleurInstitut national de la santé et de la recherche médicale (INSERM), UMR1236, Université Rennes 1, Etablissement Français du Sang Bretagne, Rennes, France.
Florence JouanInstitut national de la santé et de la recherche médicale (INSERM), UMR1236, Université Rennes 1, Etablissement Français du Sang Bretagne, Rennes, France.
Eric PinaudCentre National de la Recherche Scientifique (CNRS), UMR7276, Institut National de la Santé et de la Recherche Médicale (INSERM), UMR1262-Contrôle de la Réponse Immune B et Lymphoproliférations, Université de Limoges, Limoges, France.ORCID http://orcid.org/0000-0001-7405-9273
Karin TarteInstitut national de la santé et de la recherche médicale (INSERM), UMR1236, Université Rennes 1, Etablissement Français du Sang Bretagne, Rennes, France.ORCID http://orcid.org/0000-0002-6809-917X
Michel CognéCentre National de la Recherche Scientifique (CNRS), UMR7276, Institut National de la Santé et de la Recherche Médicale (INSERM), UMR1262-Contrôle de la Réponse Immune B et Lymphoproliférations, Université de Limoges, Limoges, France.
Silvestro G ConticelloCore Research Laboratory, ISPRO, Firenze, Italy.ORCID http://orcid.org/0000-0002-4244-1846
Evi SoutoglouGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, UK.
Ludovic DerianoGenome Integrity, Immunity and Cancer Unit, Equipe Labellisée Ligue Contre Le Cancer, INSERM U1223, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0002-9673-9525
Bernardo Reina-San-MartinInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France. reinab@igbmc.fr.ORCID http://orcid.org/0000-0003-2083-6166
Centre National de la Recherche Scientifique · FRInserm · FRUniversity of Sussex · GBIstituto di Fisiologia Clinica · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient humoral responses rely on DNA damage, mutagenesis and error-prone DNA repair. Diversification of B cell receptors through somatic hypermutation and class-switch recombination are initiated by cytidine deamination in DNA mediated by activation-induced cytidine deaminase (AID)

Indexed as

B-LymphocytesDNA Mismatch RepairImmunoglobulin Class SwitchingImmunoglobulin Switch RegionMutationSomatic Hypermutation, ImmunoglobulinAnimalsCRISPR-Cas SystemsDNA GlycosylasesFemaleGenomeMaleMiceMitochondrial ProteinsUp-RegulationUracilDNA GlycosylasesFam72a protein, mouseMitochondrial ProteinsUng protein, mouseUracil

Identifiers

PMID34819671
OpenAlexW3217630413

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.