Literature DB >> 3759087

The fragile site (16) (q22). I. Induction by AT-specific DNA-ligands and population frequency.

M Schmid, W Feichtinger, A Jessberger, J Köhler, R Lange.   

Abstract

The rare fragile site at 16q22 was experimentally induced in lymphocyte cultures with various AT-specific, non-intercalating DNA-ligands. The optimum conditions for the induction of fra(16)(q22) were determined. The best expression of fra(16)(q22) was found with the aromatic diamidine berenil which is recommended for further studies on this fragile site. The results indicate that fra(16)(q22) is a region with AT-rich, late replicating DNA. The simultaneous treatment of lymphocytes with berenil and aphidicolin (inhibitor of DNA polymerase alpha) induces both the rare fra(16)(q22) and the common fra(16)(q23) within the same chromosome. A population study on 350 unselected individuals showed that fra(16)(q22) is the most common of all rare autosomal fragile sites in man. The frequency of individuals heterozygous for fra(16)(q22) is 5.1%, no homozygosity for fra(16)(q22) was detected. Statistical analysis indicates that the population is in Hardy-Weinberg equilibrium with respect to the fragile and non-fragile chromosomes 16.

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Year:  1986        PMID: 3759087     DOI: 10.1007/bf00278788

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


  35 in total

1.  Interaction of the RNA polymerase inhibitor chromomycin with DNA.

Authors:  W Behr; K Honikel; G Hartmann
Journal:  Eur J Biochem       Date:  1969-05-01

2.  Heritable fragile sites in cancer.

Authors:  M M LeBeau; J D Rowley
Journal:  Nature       Date:  1984 Apr 12-18       Impact factor: 49.962

3.  The marker (X) syndrome: a cytogenetic and genetic analysis.

Authors:  S L Sherman; N E Morton; P A Jacobs; G Turner
Journal:  Ann Hum Genet       Date:  1984-01       Impact factor: 1.670

4.  Specific silver staining of experimentally undercondensed chromosome regions.

Authors:  T Haaf; H Weis; D Schindler; M Schmid
Journal:  Chromosoma       Date:  1984       Impact factor: 4.316

5.  The fragile site on chromosome 16 (q21q22). Data on four new families.

Authors:  F Shabtai; S Bichacho; I Halbrecht
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  Heritable fragile sites and lymphocyte culture medium containing BrdU.

Authors:  J M Scheres; T W Hustinx
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

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.  Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

9.  The use of distamycin A in human lymphocyte cultures.

Authors:  M Schmid; D A Hungerford; A Poppen; W Engel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12.

Authors:  G R Sutherland; P B Jacky; E G Baker
Journal:  Am J Hum Genet       Date:  1984-01       Impact factor: 11.025

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  15 in total

1.  Homozygotes for FRA16B are normal.

Authors:  T Hocking; W Feichtinger; M Schmid; E A Haan; E Baker; G R Sutherland
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  Fragile site (16) (q22). III. Segregation analysis.

Authors:  B Müller; W Feichtinger; C Bonaïti-Pellié; M Schmid
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

3.  Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites.

Authors:  F V Rassool; T W McKeithan; M E Neilly; E van Melle; R Espinosa; M M Le Beau
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

4.  "Spontaneous" FRA16B is a hot spot for sister chromatid exchanges.

Authors:  T Lukusa; E Meulepas; J P Fryns; H Van den Berghe; J J Cassiman
Journal:  Hum Genet       Date:  1991-09       Impact factor: 4.132

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.  Population cytogenetics of rare fragile sites in Japan.

Authors:  E Takahashi; T Hori; M Murata
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

7.  A linkage group with FRA16B (the fragile site at 16q22.1).

Authors:  J C Mulley; V J Hyland; A Fratini; L J Bates; A K Gedeon; G R Sutherland
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

8.  The fragile site (17)(p12): induction by AT-specific DNA-ligands and population cytogenetics.

Authors:  M Schmid; W Feichtinger; C Deubelbeiss; E Weller
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

9.  The fragile site (16)(q22). II. Sister chromatid exchanges.

Authors:  M Schmid; W Feichtinger; T Haaf
Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

10.  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

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