Literature DB >> 2937710

The most common fragile site in man is 3p14.

D F Smeets, J M Scheres, T W Hustinx.   

Abstract

In man a common fragile site is known to occur at 3p14. We studied the expression of this fragility in a group of 70 normal healthy subjects. Chromosome breaks, chromatid breaks and gaps at 3p14 could be observed in every examined individual, and in a total of 7000 metaphases they were seen in a mean of 4% of cells. Fluorescence studies in ten persons with chromosome No. 3 polymorphism showed that in all cases both Nos. 3 were about equally liable to breakage. A considerable variation in the fra 3p14 expression was found between individuals as well as in repeated cultures from the same person. Neither sex nor age influences could be detected. Cultures with a high percentage of lesions at 3p14 tended to have also a high number of lesions at other sites. Methotrexate and fluorodeoxyuridine markedly enhanced the expression of fra 3p14 and other fragilities. It is concluded that the chromosomal region at 3p14 represents man's most common fragile site, the expression of which seems to be influenced by environmental and heritable factors.

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Year:  1986        PMID: 2937710     DOI: 10.1007/bf00291880

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


  31 in total

1.  A folate sensitive heritable fragile site at 19p13.

Authors:  N Tommerup; J Nielsen; M Mikkelsen
Journal:  Clin Genet       Date:  1985-05       Impact factor: 4.438

2.  Involvement of band 3p14 in t(3;8) hereditary renal carcinoma.

Authors:  N Wang; K L Perkins
Journal:  Cancer Genet Cytogenet       Date:  1984-04

Review 3.  Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites.

Authors:  A de la Chapelle; R Berger
Journal:  Cytogenet Cell Genet       Date:  1984

4.  Cancer chromosome breakpoints and common fragile sites induced by aphidicolin.

Authors:  F Hecht; T W Glover
Journal:  Cancer Genet Cytogenet       Date:  1984-10

5.  Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false-negative results with the fragile(X).

Authors:  A Daniel; L Ekblom; S Phillips
Journal:  Am J Med Genet       Date:  1984-07

6.  Excess thymidine induces folate sensitive fragile sites.

Authors:  G R Sutherland; E Baker; A Fratini
Journal:  Am J Med Genet       Date:  1985-10

7.  DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.

Authors:  T W Glover; C Berger; J Coyle; B Echo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Constitutive fragile sites and cancer.

Authors:  J J Yunis; A L Soreng
Journal:  Science       Date:  1984-12-07       Impact factor: 47.728

9.  Absence of significant autosomal lesions in Huntington's disease.

Authors:  G C Beverstock; A Mol; E Wienhofer
Journal:  Ann Hum Genet       Date:  1985-10       Impact factor: 1.670

10.  Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23).

Authors:  J Whang-Peng; C S Kao-Shan; E C Lee; P A Bunn; D N Carney; A F Gazdar; J D Minna
Journal:  Science       Date:  1982-01-08       Impact factor: 47.728

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  25 in total

1.  Increased expression of 5q31 fragile site in a Bloom syndrome family.

Authors:  A F Fundia; N B Gorla; M M Bonduel; O Azpilicueta; H Lejarraga; F S Muriel; I B Larripa
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

2.  Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes.

Authors:  D F Smeets; G Merkx
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

3.  Localization of the human HF.10 finger gene on a chromosome region (3p21-22) frequently deleted in human cancers.

Authors:  E Donti; L Lanfrancone; K Huebner; A Pascucci; G Venti; G Pengue; F Grignani; C M Croce; L Lania; P G Pelicci
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

4.  Genetic determination of fragile-site expression.

Authors:  D Smeets; A Arets
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

Review 5.  Fragile sites-cytogenetic similarity with molecular diversity.

Authors:  G R Sutherland; R I Richards
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

6.  Family study of common fragile sites.

Authors:  Y Sugio; Y Kuroki
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

7.  Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysis.

Authors:  P N Rao; N A Heerema; C G Palmer
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

8.  Chromosome 3p loss of heterozygosity and mutation analysis of the FHIT and beta-cat genes in squamous cell carcinoma of the head and neck.

Authors:  M V González; M F Pello; P Ablanedo; C Suárez; V Alvarez; E Coto
Journal:  J Clin Pathol       Date:  1998-07       Impact factor: 3.411

Review 9.  DNA methylation in hepatocellular carcinoma.

Authors:  Iris Tischoff; Andrea Tannapfe
Journal:  World J Gastroenterol       Date:  2008-03-21       Impact factor: 5.742

10.  The effect of hydroxyurea on the expression of the common fragile site at 3p14.

Authors:  Z A Yan; X Z Li; X T Zhou
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

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