Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/91829
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dc.contributor.authorMontagne, L.en
dc.contributor.authorRaimondo, A.en
dc.contributor.authorDelobel, B.en
dc.contributor.authorDuban-Bedu, B.en
dc.contributor.authorNoblet, F.en
dc.contributor.authorDechaume, A.en
dc.contributor.authorBersten, D.en
dc.contributor.authorMeyre, D.en
dc.contributor.authorWhitelaw, M.en
dc.contributor.authorFroguel, P.en
dc.contributor.authorBonnefond, A.en
dc.date.issued2014en
dc.identifier.citationObesity, 2014; 22(12):2621-2624en
dc.identifier.issn1930-7381en
dc.identifier.issn1930-739Xen
dc.identifier.urihttp://hdl.handle.net/2440/91829-
dc.descriptionArticle first published online: 19 SEP 2014en
dc.description.abstractOBJECTIVE: Several deletions of chromosome 6q, including SIM1, were reported in obese patients with developmental delay. Furthermore, rare loss-of-function SIM1 mutations were shown to contribute to severe obesity, yet the role of these mutations in developmental delay remained unclear. Here, SIM1 in children with neurodevelopmental abnormalities was screened and the functional effect of the identified mutations was investigated. METHODS: SIM1 was sequenced in 283 children presenting with developmental delay and at least overweight. The effect of the identified mutations on SIM1 transcriptional activity in stable human cell lines was assessed using luciferase gene reporter assays. RESULTS: Two novel mutations (c.886A>G/p.R296G and c.925A>G/p.S309G) in two boys with variable degrees of cognitive deficits and weight issues were identified. The child mutated for p.R296G presented with a generally more severe phenotype than the p.S309G carrier (obesity, compulsive eating, neonatal hypotonia versus overweight only), while both mutations had strong loss-of-function effects on SIM1 transcriptional activity. CONCLUSIONS: Severe loss-of-function SIM1 mutations can be associated with a spectrum of developmental delay phenotypes and obesity. Our data suggest that SIM1 sequencing should be performed more systematically in patients with developmental delay, even in the absence of severe obesity. These results deserve further SIM1 screening studies.en
dc.description.statementofresponsibilityLouise Montagne, Anne Raimondo, Bruno Delobel, Bénédicte Duban-Bedu, Fanny Stutzmann Noblet, Aurélie Dechaume, David C. Bersten, David Meyre, Murray L. Whitelaw, Philippe Froguel, and Amélie Bonnefonden
dc.language.isoenen
dc.publisherWileyen
dc.rights© 2014 The Obesity Societyen
dc.subjectHumans; Obesity, Morbid; Luciferases; Repressor Proteins; DNA Mutational Analysis; Developmental Disabilities; Phenotype; Child; Female; Male; Basic Helix-Loop-Helix Transcription Factors; Transcriptional Activationen
dc.titleIdentification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delayen
dc.typeJournal articleen
dc.identifier.rmid0030012702en
dc.identifier.doi10.1002/oby.20886en
dc.identifier.pubid120413-
pubs.library.collectionMolecular and Biomedical Science publicationsen
pubs.library.teamDS03en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
Appears in Collections:Molecular and Biomedical Science publications

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