Literature DB >> 7874164

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

J E Parrish1, B A Oostra, A J Verkerk, C S Richards, J Reynolds, A S Spikes, L G Shaffer, D L Nelson.   

Abstract

Three folate-sensitive fragile sites, termed FRAXA, FRAXE and FRAXF, have been identified on the distal end of chromosome Xq. The first two contain expanded, hypermethylated and unstable CGG (or GCC) repeats within CpG islands. We now report the isolation of similar sequences responsible for the third fragile site, FRAXF. A 5-kilobase EcoRI fragment derived from a cosmid coincident with the cytogenetic anomaly detects expanded, methylated and unstable sequences in five individuals who exhibit fragile sites in distal Xq; these individuals have normal repeat lengths at both FRAXA and FRAXE. By sequence analysis, the expanded region contains a GCC repeat. PCR and sequence analysis of chromosomes from the general population indicates that the repeat is polymorphic (6 to 29 triplets), and is stable upon transmission.

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Year:  1994        PMID: 7874164     DOI: 10.1038/ng1194-229

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  39 in total

1.  Homozygotes for FRA16B are normal.

Authors:  T Hocking; W Feichtinger; M Schmid; E A Haan; E Baker; G R Sutherland
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  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

3.  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

4.  Evidence for chromosome fragility at the frataxin locus in Friedreich ataxia.

Authors:  Daman Kumari; Bruce Hayward; Asako J Nakamura; William M Bonner; Karen Usdin
Journal:  Mutat Res       Date:  2015-08-30       Impact factor: 2.433

5.  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

6.  FRAXE expansion is not a common etiological factor among developmentally delayed males.

Authors:  D J Allingham-Hawkins; P N Ray
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

7.  The enigma of common fragile sites.

Authors:  I Simonic; G S Gericke
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

8.  A heritable folate-sensitive fragile site on chromosome 2p 11.2 (FRA2L).

Authors:  S Schuffenhauer; G Lederer; J Murken
Journal:  Chromosome Res       Date:  1996-04       Impact factor: 5.239

9.  Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

Authors:  D Mishmar; A Rahat; S W Scherer; G Nyakatura; B Hinzmann; Y Kohwi; Y Mandel-Gutfroind; J R Lee; B Drescher; D E Sas; H Margalit; M Platzer; A Weiss; L C Tsui; A Rosenthal; B Kerem
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-07       Impact factor: 11.205

10.  Fragile X syndrome is less common than previously estimated.

Authors:  J E Morton; S Bundey; T P Webb; F MacDonald; P M Rindl; S Bullock
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

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