Literature DB >> 8334699

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

S J Knight1, A V Flannery, M C Hirst, L Campbell, Z Christodoulou, S R Phelps, J Pointon, H R Middleton-Price, A Barnicoat, M E Pembrey.   

Abstract

We have cloned the fragile site FRAXE and demonstrate that individuals with this fragile site possess amplifications of a GCC repeat adjacent to a CpG island in Xq28 of the human X chromosome. Normal individuals have 6-25 copies of the GCC repeat, whereas mentally retarded, FRAXE-positive individuals have > 200 copies and also have methylation at the CpG island. This situation is similar to that seen at the FRAXA locus and is another example in which a trinucleotide repeat expansion is associated with a human genetic disorder. In contrast with the fragile X syndrome, the GCC repeat can expand or contract and is equally unstable when passed through the male or female line. These results also have implications for the understanding of chromosome fragility.

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Year:  1993        PMID: 8334699     DOI: 10.1016/0092-8674(93)90300-f

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  122 in total

1.  Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability.

Authors:  A Hellman; A Rahat; S W Scherer; A Darvasi; L C Tsui; B Kerem
Journal:  Mol Cell Biol       Date:  2000-06       Impact factor: 4.272

2.  Analysis of replication timing at the FRA10B and FRA16B fragile site loci.

Authors:  O Handt; E Baker; S Dayan; S M Gartler; E Woollatt; R I Richards; R S Hansen
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

3.  The first case of the FRAXE form of inherited mental retardation in Croatia.

Authors:  Silva Hećimović; Ruzica Bago; Dubravka Muzinić; Davor Begović; Kresimir Pavelić
Journal:  Eur J Pediatr       Date:  2002-02       Impact factor: 3.183

Review 4.  Modifiers and mechanisms of multi-system polyglutamine neurodegenerative disorders: lessons from fly models.

Authors:  Moushami Mallik; Subhash C Lakhotia
Journal:  J Genet       Date:  2010-12       Impact factor: 1.166

5.  Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.

Authors:  L Basel-Vanagaite; A Alkelai; R Straussberg; N Magal; D Inbar; M Mahajna; M Shohat
Journal:  J Med Genet       Date:  2003-10       Impact factor: 6.318

6.  Silencing of metallothionein-I gene in mouse lymphosarcoma cells by methylation.

Authors:  S Majumder; K Ghoshal; Z Li; Y Bo; S T Jacob
Journal:  Oncogene       Date:  1999-11-04       Impact factor: 9.867

7.  A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.

Authors:  S J Knight; R J Ritchie; L Chakrabarti; G Cross; G R Taylor; R F Mueller; J Hurst; J Paterson; J R Yates; D J Dow; K E Davies
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

8.  Cartographic study: breakpoints in 1574 families carrying human reciprocal translocations.

Authors:  O Cohen; C Cans; M Cuillel; J L Gilardi; H Roth; M A Mermet; P Jalbert; J Demongeot
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

9.  FRAXF in a patient with chromosome 8 duplication.

Authors:  A M Vianna-Morgante; R C Mingroni-Netto; A C Barbosa; P A Otto; C Rosenberg
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

10.  A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.

Authors:  Paras Garg; Bharati Jadhav; Oscar L Rodriguez; Nihir Patel; Alejandro Martin-Trujillo; Miten Jain; Sofie Metsu; Hugh Olsen; Benedict Paten; Beate Ritz; R Frank Kooy; Jozef Gecz; Andrew J Sharp
Journal:  Am J Hum Genet       Date:  2020-09-15       Impact factor: 11.025

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