Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/73273
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorShoubridge, C.en
dc.contributor.authorTan, M.en
dc.contributor.authorSeiboth, G.en
dc.contributor.authorGecz, J.en
dc.date.issued2012en
dc.identifier.citationHuman Molecular Genetics, 2012; 21(7):1639-1647en
dc.identifier.issn0964-6906en
dc.identifier.issn1460-2083en
dc.identifier.urihttp://hdl.handle.net/2440/73273-
dc.description.abstractMutations in the Aristaless-related homeobox (ARX) gene are one of the most frequent causes of X-linked intellectual disability (ID). Several missense mutations, clustered in the paired-type homeodomain of ARX, have been identified. These mutations lead to a range of phenotypes from X-linked lissencephaly with abnormal genitalia to seizure disorders without brain malformations including X-linked infantile spasms with ID (ISSX-ID) and X-linked myoclonic epilepsy with spasticity and ID (XMESID). The effect of these mutations on the DNA-binding and transcriptional activity has been evaluated. Luciferase reporter assays showed altered repression activity of ARX by all mutations, causing brain malformations and ISSX-ID phenotypes, but not by the P353L mutation implicated in a milder phenotype of XMESID. Similarly, transient overexpression of wild-type ARX repressed endogenous expression of known ARX targets, LMO1 and SHOX2, when measured by real-time quantitative polymerase chain reaction. Overall, the molecular consequence of missense mutations correlated well with the severity of the clinical phenotype. In all mutations tested, except P353L, the DNA binding was abolished. Electrophoretic mobility shift assay results were validated using chromatin immunoprecipitation following overexpression of normal and selected missense mutations. Unlike wild-type ARX and clinically less severe mutations, the mutations leading to severe clinical phenotypes were not able to specifically bind to DNA upstream of known, endogenous ARX-regulated genes, LMO1 and SHOX2. In conclusion, the missense mutations in the ARX homeodomain represent loss-of-function mutations, which lead to a reduced or complete loss of DNA binding and as a consequence, a loss of transcriptional repression.en
dc.description.statementofresponsibilityCheryl Shoubridge, May Huey Tan, Grace Seiboth, and Jozef Géczen
dc.language.isoenen
dc.publisherOxford Univ Pressen
dc.rights© The Author 2011.en
dc.subjectCell Nucleus; Humans; DNA-Binding Proteins; Homeodomain Proteins; Transcription Factors; Repressor Proteins; DNA; Transcription, Genetic; Protein Structure, Tertiary; Active Transport, Cell Nucleus; Mutation, Missense; HEK293 Cells; LIM Domain Proteinsen
dc.titleARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repressionen
dc.typeJournal articleen
dc.identifier.rmid0020117285en
dc.identifier.doi10.1093/hmg/ddr601en
dc.identifier.pubid25524-
pubs.library.collectionPaediatrics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidShoubridge, C. [0000-0002-0157-3084]en
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.