Evidence map›Paper›PMID 21779178›Full record

ArticlePLoS genetics2011

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.

Maria Clara Bonaglia, Roberto Giorda, Silvana Beri, Cristina De Agostini, Francesca Novara, Marco Fichera, Lucia Grillo, Ornella Galesi, Annalisa Vetro, Roberto Ciccone and 45 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 4 pooled it
8.8field-weighted citation impact, top 2% 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

114 citing papers in PubMed, 4 syntheses or guidelines pooled it, 229 citations in OpenAlex.

  1. Pooled it
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  17. Updated consensus guidelines on the management of Phelan-McDermid syndrome.American journal of medical genetics. Part A · 2023
    Review
  18. Article
  19. A comprehensive map of hotspots of de novo telomere addition inbioRxiv : the preprint server for biology · 2023
    Article
  20. Article

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

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

55 authors at 20 institutions in 6 countries.

Maria Clara BonagliaCytogenetics Laboratory, Scientific Institute E. Medea, Bosisio Parini, Italy. clara.bonaglia@bp.lnf.it
Roberto Giorda
Silvana Beri
Cristina De Agostini
Francesca Novara
Marco Fichera
Lucia Grillo
Ornella Galesi
Annalisa Vetro
Roberto Ciccone
Maria Teresa Bonati
Sabrina Giglio
Renzo Guerrini
Sara Osimani
Susan Marelli
Claudio Zucca
Rita Grasso
Renato Borgatti
Elisa Mani
Cristina Motta
Massimo Molteni
Corrado Romano
Donatella Greco
Santina Reitano
Anna Baroncini
Elisabetta Lapi
Antonella Cecconi
Giulia Arrigo
Maria Grazia Patricelli
Chiara Pantaleoni
Stefano D'Arrigo
Daria Riva
Francesca Sciacca
Bernardo Dalla Bernardina
Leonardo Zoccante
Francesca Darra
Cristiano Termine
Emanuela Maserati
Stefania Bigoni
Emanuela Priolo
Armand Bottani
Stefania Gimelli
Frederique Bena
Alfredo Brusco
Eleonora di Gregorio
Irene Bagnasco
Ursula Giussani
Lucio Nitsch
Pierluigi Politi
Maria Luisa Martinez-Frias
Maria Luisa Martínez-Fernández
Nieves Martínez Guardia
Anna Bremer
Britt-Marie Anderlid
Orsetta Zuffardi
IRCCS Eugenio Medea · ITOasi Maria SS · ITUniversity of Pavia · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITAzienda Ospedaliera Universitaria Integrata Verona · ITLaboratoire de Génie Électrique et Électronique de Paris · FRMeyer Children's Hospital · ITIRCCS Ospedale San Raffaele · ITKarolinska Institutet · SEUniversidad Complutense de Madrid · ESUniversity of Insubria · ITUniversity of Turin · ITAzienda Ospedaliera S.Maria · ITCentro de Genética Clínica · PTFederico II University Hospital · ITHospital Universitario Severo Ochoa · ESIRCCS Istituto Auxologico Italiano · ITOspedale Martini · ITOspedale Santa Maria Annunziata · ITUniversity of Bergamo · IT

Funding

Telethon GGP06208
6 · The paper itself

Abstract

In this study, we used deletions at 22q13, which represent a substantial source of human pathology (Phelan/McDermid syndrome), as a model for investigating the molecular mechanisms of terminal deletions that are currently poorly understood. We characterized at the molecular level the genomic rearrangement in 44 unrelated patients with 22q13 monosomy resulting from simple terminal deletions (72%), ring chromosomes (14%), and unbalanced translocations (7%). We also discovered interstitial deletions between 17-74 kb in 9% of the patients. Haploinsufficiency of the SHANK3 gene, confirmed in all rearrangements, is very likely the cause of the major neurological features associated with PMS. SHANK3 mutations can also result in language and/or social interaction disabilities. We determined the breakpoint junctions in 29 cases, providing a realistic snapshot of the variety of mechanisms driving non-recurrent deletion and repair at chromosome ends. De novo telomere synthesis and telomere capture are used to repair terminal deletions; non-homologous end-joining or microhomology-mediated break-induced replication is probably involved in ring 22 formation and translocations; non-homologous end-joining and fork stalling and template switching prevail in cases with interstitial 22q13.3. For the first time, we also demonstrated that distinct stabilizing events of the same terminal deletion can occur in different early embryonic cells, proving that terminal deletions can be repaired by multistep healing events and supporting the recent hypothesis that rare pathogenic germline rearrangements may have mitotic origin. Finally, the progressive clinical deterioration observed throughout the longitudinal medical history of three subjects over forty years supports the hypothesis of a role for SHANK3 haploinsufficiency in neurological deterioration, in addition to its involvement in the neurobehavioral phenotype of PMS.

Indexed as

Chromosome DeletionAdolescentAdultAgedAged, 80 and overBase SequenceChildChild, PreschoolChromosome DisordersChromosomes, Human, Pair 22Comparative Genomic HybridizationFemaleHumansInfantInfant, NewbornMale

Identifiers

PMID21779178
PMCPMC3136441
OpenAlexW2144839123

What OpenQuestion holds

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LicenceCC BY
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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.