Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/11493
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dc.contributor.authorGecz, J.en
dc.contributor.authorGedeon, A.en
dc.contributor.authorSutherland, G.en
dc.contributor.authorMulley, J.en
dc.date.issued1996en
dc.identifier.citationNature Genetics, 1996; 13(1):105-108en
dc.identifier.issn1061-4036en
dc.identifier.issn1546-1718en
dc.identifier.urihttp://hdl.handle.net/2440/11493-
dc.description.abstractFive folate-sensitive fragile sites have been characterized at the molecular level (FRAXA, FRAXE, FRAXF, FRA16A and FRA11B). Three of them (FRAXA, FRAXE and FRA11B) are associated with clinical problems, and two of the genes (FMR1 in FRAXA and CBL2 in FRA11B) have been identified. All of these fragile sites are associated with (CCG)n/(CGG)n triplet expansions which are hypermethylated beyond a critical size. FRAXE is a rare folate sensitive fragile site only recently recognized. Its cytogenetic expression was found to involve the amplification of a (CCG)n repeat adjacent to a CpG island. Normal alleles vary from 6 to 25 copies. Expansions of greater than 200 copies were found in FRAXE expressing males and their FRAXE associated CpG island was fully methylated. An association of FRAXE expression with concurrent methylation of the CpG island and mild non-specific mental handicap in males has been reported by several groups. We now report the cloning and characterization of a gene (FMR2) adjacent to FRAXE. Elements of FMR2 were initially identified from sequences deleted from a developmentally delayed boy. We correlate loss of FMR2 expression with (CCG)n expansion at FRAXE, demonstrating that this is a gene associated with the CpG island adjacent to FRAXE and contributes for FRAXE-associated mild mental retardation.en
dc.description.statementofresponsibilityJozef Gecz, Agi K. Gedeon, Grant R. Sutherland & John C. Mulleyen
dc.language.isoenen
dc.publisherNature Publishing Groupen
dc.rights© 1996 Nature Publishing Groupen
dc.subjectBrain; Chromosomes, Artificial, Yeast; Fetus; Humans; Mental Retardation; Fragile X Syndrome; Proteins; Trans-Activators; Nuclear Proteins; DNA Probes; Dinucleoside Phosphates; DNA Primers; Polymerase Chain Reaction; Pedigree; Gene Expression; Amino Acid Sequence; Base Sequence; Repetitive Sequences, Nucleic Acid; Sequence Homology, Amino Acid; Polymorphism, Genetic; Gene Library; Exons; Molecular Sequence Data; Child; Female; Maleen
dc.titleIdentification of the gene FMR2, associated with FRAXE mental retardationen
dc.typeJournal articleen
dc.identifier.rmid0030004272en
dc.identifier.doi10.1038/ng0596-105en
dc.identifier.pubid68278-
pubs.library.collectionGenetics publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Genetics publications

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