Literature DB >> 2037282

Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes.

D F Smeets1, G F Merkx, A H Hopman.   

Abstract

The presence of DA/DAPI (distamycin A/4,6-diamino-2-phenyl-indole) heteromorphism on the short arm of human acrocentric chromosomes was investigated in 127 individuals. In 7 cases, a DA/DAPI signal was observed on an acrocentric chromosome other than 15. Subsequently, in situ hybridization (ISH) with a pericentromeric probe specific for chromosome 15 was carried out. In all 7 cases, three ISH signals were present in every metaphase, i.e., on both chromosomes 15 and on the third DA/DAPI-fluorescence-positive acrocentric chromosome (a chromosome 13 or 14), indicating that a chromosome 15 short arm was also present on these chromosomes. Therefore, we conclude that translocations of short arm sequences from chromosome 15 onto other D-group chromosomes occur frequently. Moreover, it appears that DA/DAPI staining remains specific for the short arm of chromosome 15, despite a number of recent papers suggesting otherwise.

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Year:  1991        PMID: 2037282     DOI: 10.1007/bf01213090

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


  11 in total

1.  Evidence for specificity of the DA/DAPI technique.

Authors:  G F Merkx; A H Hopman; A C Akkermans-Scholten; D F Smeets
Journal:  Cytogenet Cell Genet       Date:  1990

2.  Evidence for lack of specificity of the DA/DAPI technique.

Authors:  A Pérez-Castillo; M A Martín-Lucas; J A Abrisqueta
Journal:  Cytogenet Cell Genet       Date:  1987

3.  Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique.

Authors:  A Babu; M J Macera; R S Verma
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

4.  Lack of specificity of DA/DAPI fluorescence.

Authors:  M S Lin; K H Huynh; A Fujimoto; M G Wilson
Journal:  Clin Genet       Date:  1990-01       Impact factor: 4.438

5.  Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15.

Authors:  M J Higgins; H S Wang; I Shtromas; T Haliotis; J C Roder; J J Holden; B N White
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

6.  Location of ribosomal DNA in the human chromosome complement.

Authors:  A S Henderson; D Warburton; K C Atwood
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

7.  Ribosomal cistrons and acrocentric chromosomes in man.

Authors:  K Bross; W Krone
Journal:  Humangenetik       Date:  1973-03-23

8.  Double in situ hybridization in combination with digital image analysis: a new approach to study interphase chromosome topography.

Authors:  P Emmerich; P Loos; A Jauch; A H Hopman; J Wiegant; M J Higgins; B N White; M van der Ploeg; C Cremer; T Cremer
Journal:  Exp Cell Res       Date:  1989-03       Impact factor: 3.905

9.  Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

Authors:  D Schweizer; P Ambros; M Andrle
Journal:  Exp Cell Res       Date:  1978-02       Impact factor: 3.905

10.  In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors.

Authors:  A H Hopman; F C Ramaekers; A K Raap; J L Beck; P Devilee; M van der Ploeg; G P Vooijs
Journal:  Histochemistry       Date:  1988
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  10 in total

1.  Chromosome 15p marker D15Z1 frequently maps to the short arm of other D-group chromosomes.

Authors:  D F Smeets; G F Merkx; A H Hopman
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

2.  High population incidence of the 15p marker D15Z1 mapping to the short arm of one homologue 14.

Authors:  K Stergianou; C P Gould; J J Waters; M Hultén
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

3.  Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes.

Authors:  T A Wilkinson; J A Crolla
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

Review 4.  Detection of genomic changes in cancer by in situ hybridization.

Authors:  A H Hopman; C E Voorter; F C Ramaekers
Journal:  Mol Biol Rep       Date:  1994-01       Impact factor: 2.316

5.  Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs).

Authors:  H Kühl; S Röttger; H Heilbronner; H Enders; W Schempp
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

6.  A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.

Authors:  Annette E Cockwell; Patricia A Jacobs; Sarah J Beal; John A Crolla
Journal:  Hum Genet       Date:  2003-01-08       Impact factor: 4.132

7.  Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes.

Authors:  R Plattner; N A Heerema; Y B Yurov; C G Palmer
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

8.  A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

Authors:  J A Crolla; N R Dennis; P A Jacobs
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

9.  Somatic pairing of centromeres and short arms of chromosome 15 in the hematopoietic and lymphoid system.

Authors:  J P Lewis; H J Tanke; A K Raap; G C Beverstock; H C Kluin-Nelemans
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132

10.  Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome.

Authors:  O Bartsch; U König; M B Petersen; H Poulsen; M Mikkelsen; F Palau; F Prieto; E Schwinger
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

  10 in total

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