Graded Otx2 activities demonstrate dose-sensitive eye and retina phenotypes

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dc.contributor.authorBernard, Clemenceko
dc.contributor.authorKim, Hyoung Taiko
dc.contributor.authorIbad, Raoul Toreroko
dc.contributor.authorLee, Eun Jungko
dc.contributor.authorSimonutti, Manuelko
dc.contributor.authorPicaud, Sergeko
dc.contributor.authorAcampora, Darioko
dc.contributor.authorSimeone, Antonioko
dc.contributor.authorDi Nardo, Ariel A.ko
dc.contributor.authorProchiantz, Alainko
dc.contributor.authorMoya, Kenneth L.ko
dc.contributor.authorKim, Jin Wooko
dc.date.accessioned2014-08-29T02:07:53Z-
dc.date.available2014-08-29T02:07:53Z-
dc.date.created2014-05-20-
dc.date.created2014-05-20-
dc.date.issued2014-04-
dc.identifier.citationHUMAN MOLECULAR GENETICS, v.23, no.7, pp.1742 - 1753-
dc.identifier.issn0964-6906-
dc.identifier.urihttp://hdl.handle.net/10203/188981-
dc.description.abstractIn the human, mutations of OTX2 (Orthodenticle homeobox 2 transcription factor) translate into eye malformations of variable expressivity (even between the two eyes of the same individual) and incomplete penetrance, suggesting the existence of subtle thresholds in OTX2 activity. We have addressed this issue by analyzing retinal structure and function in six mutant mice with graded Otx2 activity: Ofx2(+/+), Otx2(+/AA), Otx2(+/GFP), Otx2(AA/AA), Otx2(AA/GFP) and OtX2(GFP/GFP). Null mice (Otx2(GFP/GFP)) fail to develop the head and are embryonic lethal, and compound heterozygous Otx2(AA/GFP) mice show a truncated head and die at birth. All other genotypes develop until adulthood. We analyzed eye structure and visual physiology in the genotypes that develop until adulthood and report that phenotype severity parallels Otx2 activity. Otx2(+/AA) are only mildly affected whereas Otx2(+/GFP) are more affected than Otx2(+/AA) but less than Otx2(AA/AA) mice. Otx2(AA/AA) mice later manifest the most severe defects, with variable expressivity. Electrophysiological and histological analyses of the mouse retina revealed progressive death of bipolar cells and cone photoreceptors that is both Otx2 activity- and age-dependent with the same ranking of phenotypic severity. This study demonstrates the importance of gene dosage in the development of age-dependent pathologies and underscores the fact that small gene dosage differences can cause significant pathological states.-
dc.languageEnglish-
dc.publisherOXFORD UNIV PRESS-
dc.subjectPHOTORECEPTOR CELL FATE-
dc.subjectVISUAL-CORTEX-
dc.subjectPLASTICITY-
dc.subjectGENE-
dc.subjectMUTATIONS-
dc.subjectBINDING-
dc.subjectSPECIFICATION-
dc.subjectTRANSCRIPTION-
dc.subjectGASTRULATION-
dc.subjectHOMEOPROTEIN-
dc.titleGraded Otx2 activities demonstrate dose-sensitive eye and retina phenotypes-
dc.typeArticle-
dc.identifier.wosid000333267900006-
dc.identifier.scopusid2-s2.0-84906078169-
dc.type.rimsART-
dc.citation.volume23-
dc.citation.issue7-
dc.citation.beginningpage1742-
dc.citation.endingpage1753-
dc.citation.publicationnameHUMAN MOLECULAR GENETICS-
dc.identifier.doi10.1093/hmg/ddt562-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorKim, Jin Woo-
dc.contributor.nonIdAuthorBernard, Clemence-
dc.contributor.nonIdAuthorIbad, Raoul Torero-
dc.contributor.nonIdAuthorSimonutti, Manuel-
dc.contributor.nonIdAuthorPicaud, Serge-
dc.contributor.nonIdAuthorAcampora, Dario-
dc.contributor.nonIdAuthorSimeone, Antonio-
dc.contributor.nonIdAuthorDi Nardo, Ariel A.-
dc.contributor.nonIdAuthorProchiantz, Alain-
dc.contributor.nonIdAuthorMoya, Kenneth L.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusPHOTORECEPTOR CELL FATE-
dc.subject.keywordPlusVISUAL-CORTEX-
dc.subject.keywordPlusPLASTICITY-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusSPECIFICATION-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusGASTRULATION-
dc.subject.keywordPlusHOMEOPROTEIN-
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