Literature DB >> 2579891

New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridine.

G R Sutherland, M I Parslow, E Baker.   

Abstract

Two new classes of common fragile site seen in chromosomes from blood lymphocyte cultures are reported. The first class is induced in bands 1q42 and 19q13 by 5-azacytidine (5-AZA). Maximum induction of these fragile sites occurs when the 5-AZA is added 5-8h prior to harvest. The second class is induced in bands 6q13, 9p21, and 10q21 by bromodeoxyuridine (BrdU). In this instance maximum induction occurred if the BrdU was added 4-6h prior to harvest. The known fragile sites, both rare and common, are summarised.

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Year:  1985        PMID: 2579891     DOI: 10.1007/bf00293031

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


  10 in total

1.  Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

2.  On the induction of segment extension and chromatid structural changes in Vicia faba chromosomes after treatment with 5-azacytidine and 5-azadeoxycytidine.

Authors:  V Fucík; A Michaelis; R Rieger
Journal:  Mutat Res       Date:  1970-06       Impact factor: 2.433

3.  Fragile sites and predisposition to leukemia and lymphoma.

Authors:  J J Yunis
Journal:  Cancer Genet Cytogenet       Date:  1984-05

4.  Segmentation of human chromosomes induced by 5-ACR (5-azacytidine).

Authors:  E Viegas-Péquignot; B Dutrillaux
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

Review 5.  The fragile X chromosome.

Authors:  G R Sutherland
Journal:  Int Rev Cytol       Date:  1983

6.  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

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.  Detection of G-C rich heterochromatin by 5-azacytidine in mammals.

Authors:  E Viegas-Péquignot; B Dutrillaux
Journal:  Hum Genet       Date:  1981       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

  10 in total
  23 in total

1.  Hypermethylation of human DNA sequences in embryonal carcinoma cells and somatic tissues but not in sperm.

Authors:  X Y Zhang; P T Loflin; C W Gehrke; P A Andrews; M Ehrlich
Journal:  Nucleic Acids Res       Date:  1987-11-25       Impact factor: 16.971

2.  Homozygous condition for a BrdU-requiring fragile site on chromosome 12.

Authors:  I Voiculescu; E Back; W Schempp
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

3.  Inhibition of condensation in human chromosomes induced by the thymidine analogue 5-iododeoxyuridine.

Authors:  G Ott; T Haaf; M Schmid
Journal:  Chromosome Res       Date:  1998-09       Impact factor: 5.239

4.  A BrdU-requiring fragile site on chromosome 12.

Authors:  I Voiculescu; C Hausmann; G Wolff; E Back
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

5.  Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts.

Authors:  A Kuwano; I Murano; T Kajii
Journal:  Hum Genet       Date:  1990-05       Impact factor: 4.132

6.  Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells.

Authors:  I Murano; A Kuwano; T Kajii
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

7.  Increased frequencies of sister chromatid exchanges at common fragile sites (1)(q42) and (19)(q13).

Authors:  W Feichtinger; M Schmid
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

8.  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

9.  Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.

Authors:  E Rossi; G Floridia; M Casali; C Danesino; G Chiumello; F Bernardi; I Magnani; L Papi; M Mura; O Zuffardi
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

10.  DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells.

Authors:  M Gandhi; L W Dillon; S Pramanik; Y E Nikiforov; Y-H Wang
Journal:  Oncogene       Date:  2010-01-25       Impact factor: 9.867

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