Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series
Identifieur interne : 002B56 ( Ncbi/Curation ); précédent : 002B55; suivant : 002B57Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series
Auteurs : J. Van De Leemput [États-Unis, Royaume-Uni] ; F. Wavrant-De Vrièze [États-Unis] ; I. Rafferty [États-Unis] ; Jm Bras [États-Unis] ; P. Giunti [Royaume-Uni] ; Emc Fisher [Royaume-Uni] ; J. Hardy [Royaume-Uni] ; Ab Singleton [États-Unis] ; H. Houlden [Royaume-Uni]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2010.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Inositol 1,4,5-Trisphosphate Receptors.
- classification : Spinocerebellar Ataxias.
- genetics : Exons, Point Mutation, Spinocerebellar Ataxias.
- methods : Sequence Analysis, DNA.
- Adolescent, Adult, Cohort Studies, Female, Humans, Male, Middle Aged, Young Adult.
Abstract
Spinocerebellar ataxia type 15 and 16 (SCA15/16) are autosomal dominant cerebellar ataxias that are slowly progressive with a predominantly pure ataxia phenotype (ADCA III). The locus for SCA15 was first mapped to 3p24.2–3pter and subsequently full or partial deletions in the
Url:
DOI: 10.1002/mds.22970
PubMed: 20437544
PubMed Central: 2864955
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PMC:2864955Le document en format XML
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</affiliation>
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</affiliation>
</author>
<author><name sortKey="Giunti, P" sort="Giunti, P" uniqKey="Giunti P" first="P" last="Giunti">P. Giunti</name>
<affiliation wicri:level="1"><nlm:aff id="A2"> Department of Molecular Neuroscience and Reta Lila Weston Laboratories, Institute of Neurology, UCL, Queen Square House, London WC1N 3BG, United Kingdom</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
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</affiliation>
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<author><name sortKey="Fisher, Emc" sort="Fisher, Emc" uniqKey="Fisher E" first="Emc" last="Fisher">Emc Fisher</name>
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<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea> Department of Neurodegenerative Disease, Institute of Neurology, UCL, Queen Square House, London WC1N 3BG</wicri:regionArea>
<wicri:noRegion>London WC1N 3BG</wicri:noRegion>
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</author>
<author><name sortKey="Hardy, J" sort="Hardy, J" uniqKey="Hardy J" first="J" last="Hardy">J. Hardy</name>
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<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea> Department of Molecular Neuroscience and Reta Lila Weston Laboratories, Institute of Neurology, UCL, Queen Square House, London WC1N 3BG</wicri:regionArea>
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</affiliation>
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<author><name sortKey="Singleton, Ab" sort="Singleton, Ab" uniqKey="Singleton A" first="Ab" last="Singleton">Ab Singleton</name>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea> Laboratory of Neurogenetics, National Institute on Aging, National Institutes ofHealth, 35 Convent Drive, 20892, Bethesda, MD</wicri:regionArea>
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</affiliation>
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<author><name sortKey="Houlden, H" sort="Houlden, H" uniqKey="Houlden H" first="H" last="Houlden">H. Houlden</name>
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<wicri:noRegion>London WC1N 3BG</wicri:noRegion>
</affiliation>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Cohort Studies</term>
<term>Exons (genetics)</term>
<term>Female</term>
<term>Humans</term>
<term>Inositol 1,4,5-Trisphosphate Receptors (genetics)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Point Mutation (genetics)</term>
<term>Sequence Analysis, DNA (methods)</term>
<term>Spinocerebellar Ataxias (classification)</term>
<term>Spinocerebellar Ataxias (genetics)</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Inositol 1,4,5-Trisphosphate Receptors</term>
</keywords>
<keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Spinocerebellar Ataxias</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Exons</term>
<term>Point Mutation</term>
<term>Spinocerebellar Ataxias</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Sequence Analysis, DNA</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Young Adult</term>
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<front><div type="abstract" xml:lang="en"><p id="P1">Spinocerebellar ataxia type 15 and 16 (SCA15/16) are autosomal dominant cerebellar ataxias that are slowly progressive with a predominantly pure ataxia phenotype (ADCA III). The locus for SCA15 was first mapped to 3p24.2–3pter and subsequently full or partial deletions in the <italic>inositol 1,4,5-triphosphate receptor type 1</italic>
(<italic>ITPR1</italic>
) gene were identified in several ADCA III families that segregated with the disease. A single missense coding variant has been described, but the pathogenicity of this change has not been proven. We sequenced the entire coding region and flanking regions of <italic>ITPR1</italic>
in unrelated ADCA III families (<italic>n</italic>
=38) that were negative for large deletions on whole genome arrays, and for which SCAs 1, 2, 3, 6, 7, 8, 11, 12, 14, 17 and the Friedreich’s ataxia expansion were excluded in all probands. Mutation at SCA5, 10 and 27 was also excluded in some families. A number of coding and non-coding polymorphisms were identified but no <italic>ITPR1</italic>
mutations were found. The results indicate that point mutations in <italic>ITPR1</italic>
are at best a rare cause of ADCA III.</p>
</div>
</front>
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