Literature DB >> 2227930

Variability in expression of common fragile sites: in search of a new criterion.

D K Jordan1, T L Burns, J E Divelbiss, R F Woolson, S R Patil.   

Abstract

Fragile sites are nonrandom, heritable sites on chromosomes that can be induced to form gaps, breaks, and rearrangements under specific conditions. There is currently no established criterion to define a common fragile site. We applied seven published criteria to our data from three groups of subjects: (1) three pairs of like-sexed twins, (2) four unaffected von Hippel-Lindau (VHL) family members, and (3) six patients affected with VHL disease. Substantial differences were present in the numbers of sites considered positive by these criteria. While some of this variability can be attributed to technical factors, our data illustrate the problems in comparing results from different studies to assess the significance of fragile sites. A recently published criterion is based upon the Poisson distribution. We found this criterion to be flawed in its presentation, and furthermore, the Poisson distribution did not provide an adequate approximation to our data. We propose here an alternative approach based upon the negative binomial distribution.

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Year:  1990        PMID: 2227930     DOI: 10.1007/bf00194217

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


  12 in total

Review 1.  Report of the committee on cytogenetic markers.

Authors:  G R Sutherland; D H Ledbetter
Journal:  Cytogenet Cell Genet       Date:  1989

2.  Fragile sites and genitourinary tumors.

Authors:  E H Tajara; B K Hecht; D Lockwood; H Bixenman; C S Berger; A A Sandberg; F Hecht
Journal:  Cancer Genet Cytogenet       Date:  1988-03

3.  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

4.  Fragile sites are targets of diverse mutagens and carcinogens.

Authors:  J J Yunis; A L Soreng; A E Bowe
Journal:  Oncogene       Date:  1987-03       Impact factor: 9.867

Review 5.  Chromosomal fragile sites and cancer-specific rearrangements.

Authors:  M M Le Beau
Journal:  Blood       Date:  1986-04       Impact factor: 22.113

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

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

7.  Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures.

Authors:  A P Craig-Holmes; L C Strong; A Goodacre; S Pathak
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

8.  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

9.  Fragile sites and cancer breakpoints.

Authors:  F Hecht; G R Sutherland
Journal:  Cancer Genet Cytogenet       Date:  1984-06

10.  The chromosomal basis of human neoplasia.

Authors:  J J Yunis
Journal:  Science       Date:  1983-07-15       Impact factor: 47.728

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  2 in total

1.  The enigma of common fragile sites.

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

2.  Identifying chromosomal fragile sites from individuals: a multinomial statistical model.

Authors:  U Böhm; P F Dahm; B F McAllister; I F Greenbaum
Journal:  Hum Genet       Date:  1995-03       Impact factor: 4.132

  2 in total

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