Literature DB >> 7152523

Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome.

S Scappaticci, D Cerimele, M Fraccaro.   

Abstract

The cytogenetics of six cases of adult progeria (Werner's syndrome) from three Sardinian families were investigated. The overall increased incidence of chromosome breakage found in cultured lymphocytes and fibroblasts seems to be age-dependent. The occurrence of clonal variegated translocation mosaicism, previously found by other authors in fibroblast cell lines derived from Werner patients was demonstrated also in fibroblasts analyzed in situ on the outgrowth halos from primary skin explants; a strong indication that these aberrations are present in the in vivo precursors. The same type of clonal structural aberration was found for the first time also in 72h-cultured lymphocytes. These findings demonstrate that Werner's syndrome is indeed a further example of a chromosome rearrangement syndrome.

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Year:  1982        PMID: 7152523     DOI: 10.1007/bf00295599

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  9 in total

1.  Cellular aging in Werner's syndrome: a unique phenotype?

Authors:  T H Norwood; H Hoehn; D Salk; G M Martin
Journal:  J Invest Dermatol       Date:  1979-07       Impact factor: 8.551

2.  Aneuploidy and ageing: chromosome studies on a random sample of the population using G-banding.

Authors:  S M Galloway; K E Buckton
Journal:  Cytogenet Cell Genet       Date:  1978

3.  Sister chromatid exchange frequencies in Progeria and Werner syndrome patients.

Authors:  G J Darlington; R Dutkowski; W T Brown
Journal:  Am J Hum Genet       Date:  1981-09       Impact factor: 11.025

4.  Evidence of clonal attenuation, clonal succession, and clonal expansion in mass cultures of aging Werner's syndrome skin fibroblasts.

Authors:  D Salk; K Au; H Hoehn; M R Stenchever; G M Martin
Journal:  Cytogenet Cell Genet       Date:  1981

5.  High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency.

Authors:  D Cerimele; F Cottoni; S Scappaticci; G Rabbiosi; G Borroni; E Sanna; G Zei; M Fraccaro
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

6.  Chromosome breaks in Werner's syndrome and their prevention in vitro by radical-scavenging enzymes.

Authors:  I Nordenson
Journal:  Hereditas       Date:  1977       Impact factor: 3.271

7.  A mechanism of x chromosome aneuploidy in lymphocytes of aging women.

Authors:  P H Fitzgerald
Journal:  Humangenetik       Date:  1975-06-19

8.  Variegated translocation mosaicism in human skin fibroblast cultures.

Authors:  H Hoehn; E M Bryant; K Au; T H Norwood; H Boman; G M Martin
Journal:  Cytogenet Cell Genet       Date:  1975

9.  Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.

Authors:  D Salk; K Au; H Hoehn; G M Martin
Journal:  Cytogenet Cell Genet       Date:  1981
  9 in total
  25 in total

1.  Mutations in the WRN gene in mice accelerate mortality in a p53-null background.

Authors:  D B Lombard; C Beard; B Johnson; R A Marciniak; J Dausman; R Bronson; J E Buhlmann; R Lipman; R Curry; A Sharpe; R Jaenisch; L Guarente
Journal:  Mol Cell Biol       Date:  2000-05       Impact factor: 4.272

2.  Telomere instability in a human tumor cell line expressing a dominant-negative WRN protein.

Authors:  Yongli Bai; John P Murnane
Journal:  Hum Genet       Date:  2003-06-25       Impact factor: 4.132

3.  Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Authors:  C E Yu; J Oshima; E M Wijsman; J Nakura; T Miki; C Piussan; S Matthews; Y H Fu; J Mulligan; G M Martin; G D Schellenberg
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

4.  RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli.

Authors:  K Hanada; T Ukita; Y Kohno; K Saito; J Kato; H Ikeda
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

5.  Chromosome translocations in fibroblast cultures derived from patients with Werner's syndrome.

Authors:  P A Benn
Journal:  Am J Hum Genet       Date:  1985-01       Impact factor: 11.025

6.  The Werner Syndrome Helicase Coordinates Sequential Strand Displacement and FEN1-Mediated Flap Cleavage during Polymerase δ Elongation.

Authors:  Baomin Li; Sita Reddy; Lucio Comai
Journal:  Mol Cell Biol       Date:  2017-01-19       Impact factor: 4.272

7.  Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations.

Authors:  S Schonberg; M F Niermeijer; D Bootsma; E Henderson; J German
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

Review 8.  Werner's syndrome: a review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations.

Authors:  D Salk
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  Lymphocyte proliferation and nucleoid sedimentation in a case of premature aging distinct from Werner's syndrome.

Authors:  M A Kim; R Happle; H Traupe
Journal:  Arch Dermatol Res       Date:  1986       Impact factor: 3.017

Review 10.  From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.

Authors:  L S Cox; R G A Faragher
Journal:  Cell Mol Life Sci       Date:  2007-10       Impact factor: 9.261

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