Literature DB >> 7561966

Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm.

A Massari1, M Gennarelli, E Menegazzo, A Pizzuti, V Silani, I Mastrogiacomo, E Pagani, C Angelini, G Scarlato, G Novelli.   

Abstract

We have analysed the [AGC] expansion in leucocytes, muscle and sperm from 17 individuals affected by myotonic dystrophy (DM). Skeletal muscle showed a larger repeat number than leucocytes in the same patient. A similar degree of expansion was detected in differently affected muscles of a single patient. The germline mutation (< or = 350 repeats) was expanded in somatic cells of the progeny in all patients examined. Our results provide evidence of an early postzygotic instability of the [AGC] repeat in DM.

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Year:  1995        PMID: 7561966     DOI: 10.1007/BF00868393

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  37 in total

Review 1.  Triplet repeat mutations in human disease.

Authors:  C T Caskey; A Pizzuti; Y H Fu; R G Fenwick; D L Nelson
Journal:  Science       Date:  1992-05-08       Impact factor: 47.728

2.  Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

Authors:  D Wöhrle; I Hennig; W Vogel; P Steinbach
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

3.  Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair.

Authors:  M Strand; T A Prolla; R M Liskay; T D Petes
Journal:  Nature       Date:  1993-09-16       Impact factor: 49.962

4.  Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.

Authors:  J B Redman; R G Fenwick; Y H Fu; A Pizzuti; C T Caskey
Journal:  JAMA       Date:  1993-04-21       Impact factor: 56.272

5.  The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

Authors:  E Reyniers; L Vits; K De Boulle; B Van Roy; D Van Velzen; E de Graaff; A J Verkerk; H Z Jorens; J K Darby; B Oostra
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

6.  Somatic instability of CTG repeat in myotonic dystrophy.

Authors:  T Ashizawa; J R Dubel; Y Harati
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

7.  Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.

Authors:  P Shelbourne; R Winqvist; E Kunert; J Davies; J Leisti; H Thiele; H Bachmann; J Buxton; B Williamson; K Johnson
Journal:  Hum Mol Genet       Date:  1992-10       Impact factor: 6.150

8.  Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Authors:  R Koide; T Ikeuchi; O Onodera; H Tanaka; S Igarashi; K Endo; H Takahashi; R Kondo; A Ishikawa; T Hayashi
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

9.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors:  J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

Review 10.  The dynamic genomics of myotonic dystrophy and its clinical relevance: an overview.

Authors:  G Novelli; M Gennarelli; C Fattorini; C Abbruzzese; B Dallapiccola
Journal:  Biomed Pharmacother       Date:  1993       Impact factor: 6.529

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  2 in total

1.  Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene.

Authors:  M B Delatycki; D Paris; R J Gardner; K Forshaw; G A Nicholson; N Nassif; R Williamson; S M Forrest
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

2.  CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.

Authors:  Lise Barbé; Stella Lanni; Arturo López-Castel; Silvie Franck; Claudia Spits; Kathelijn Keymolen; Sara Seneca; Stephanie Tomé; Ioana Miron; Julie Letourneau; Minggao Liang; Sanaa Choufani; Rosanna Weksberg; Michael D Wilson; Zdenek Sedlacek; Cynthia Gagnon; Zuzana Musova; David Chitayat; Patrick Shannon; Jean Mathieu; Karen Sermon; Christopher E Pearson
Journal:  Am J Hum Genet       Date:  2017-03-02       Impact factor: 11.025

  2 in total

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