Literature DB >> 8659523

Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.

B A Sullivan1, L S Jenkins, E M Karson, J Leana-Cox, S Schwartz.   

Abstract

Most Robertsonian translocations are dicentric, suggesting that the location of chromosomal breaks leading to their formation occur in the acrocentric short arm. Previous cytogenetic and molecular cytogenetic studies have shown that few Robertsonian translocations retain ribosomal genes or beta-satellite DNA. Breakpoints in satellite III DNA, specifically between two chromosome 14-specific subfamilies, pTRS-47 and pTRS-63, have been indicated for most of the dicentric 14q21q and 13q14q translocations that have been studied. We have analyzed the structure of 36 dicentric translocations, using several repetitive DNA probes that localize to the acrocentric short arm. The majority of the translocations retained satellite III DNA, while others proved variable in structure. Of 10 14q21q translocations analyzed, satellite III DNA was undetected in 1; 6 retained one satellite III DNA subfamily, pTRS-47; and 3 appeared to contain two 14-specific satellite III DNA sub-families, pTRS-47 and pTRS-63. In 10/11 translocations involving chromosome 15, the presence of satellite III DNA was observed. Our results show that various regions of the acrocentric short arm, and, particularly, satellite III DNA sequences, are involved in the formation of Robertsonian translocations.

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Year:  1996        PMID: 8659523      PMCID: PMC1915107     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  24 in total

1.  Structure and inheritance of some heterozygous Robertsonian translocation in man.

Authors:  A Daniel; P R Lam-Po-Tang
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

2.  Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15.

Authors:  K H Choo; E Earle; B Vissel; R G Filby
Journal:  Genomics       Date:  1990-06       Impact factor: 5.736

3.  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

4.  Random acrocentric bivalent associations in human pachytene spermatocytes. Molecular implications in the occurrence of Robertsonian translocations.

Authors:  M R Guichaoua; M Devictor; M Hartung; J M Luciani; A Stahl
Journal:  Cytogenet Cell Genet       Date:  1986

5.  Dicentric and monocentric Robertsonian translocations in man.

Authors:  E Niebuhr
Journal:  Humangenetik       Date:  1972

6.  Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.

Authors:  J R Gosden; S S Lawrie; C M Gosden
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025

7.  Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocations.

Authors:  K H Choo; B Vissel; R Brown; R G Filby; E Earle
Journal:  Nucleic Acids Res       Date:  1988-02-25       Impact factor: 16.971

8.  Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.

Authors:  M A Anderson; J F Gusella
Journal:  In Vitro       Date:  1984-11

9.  Nucleolus organizer regions in translocations involving acrocentric chromosomes.

Authors:  M Mikkelsen; A Basli; H Poulsen
Journal:  Cytogenet Cell Genet       Date:  1980

Review 10.  The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations.

Authors:  E Therman; B Susman; C Denniston
Journal:  Ann Hum Genet       Date:  1989-01       Impact factor: 1.670

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  22 in total

1.  Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Authors:  L A Christ; C A Crowe; M A Micale; J M Conroy; S Schwartz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome.

Authors:  J E Horvath; S Schwartz; E E Eichler
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

Review 3.  Parental origin and timing of de novo Robertsonian translocation formation.

Authors:  Ruma Bandyopadhyay; Anita Heller; Cami Knox-DuBois; Christopher McCaskill; Sue Ann Berend; Scott L Page; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-11-06       Impact factor: 11.025

4.  Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.

Authors:  J M Conroy; T A Grebe; L A Becker; K Tsuchiya; R D Nicholls; K Buiting; B Horsthemke; S B Cassidy; S Schwartz
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

5.  Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome.

Authors:  Sheng-Wen Shaw; Chih-Ping Chen; Po-Jen Cheng; Tzu-Hao Wang; Jia-Woei Hou; Cheng-Tao Lin; Shuenn-Dhy Chang; Hsiao-Lin Hwa; Ju-Li Lin; An-Shine Chao; Yung-Kuei Soong; Fon-Jou Hsieh
Journal:  J Hum Genet       Date:  2007-12-12       Impact factor: 3.172

6.  Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomes.

Authors:  S A Berend; J Horwitz; C McCaskill; L G Shaffer
Journal:  Am J Hum Genet       Date:  2000-04-19       Impact factor: 11.025

7.  Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: genotype-phenotype correlations.

Authors:  Thomas P Slavin; Kevin Kuruvilla; Christine A Curtis; Laurie A Christ; Anna L Mitchell
Journal:  Am J Med Genet A       Date:  2011-02-22       Impact factor: 2.802

8.  Chromosome stability is maintained by short intercentromeric distance in functionally dicentric human Robertsonian translocations.

Authors:  S L Page; L G Shaffer
Journal:  Chromosome Res       Date:  1998-02       Impact factor: 5.239

9.  Telomere disruption results in non-random formation of de novo dicentric chromosomes involving acrocentric human chromosomes.

Authors:  Kaitlin M Stimpson; Ihn Young Song; Anna Jauch; Heidi Holtgreve-Grez; Karen E Hayden; Joanna M Bridger; Beth A Sullivan
Journal:  PLoS Genet       Date:  2010-08-12       Impact factor: 5.917

10.  Genomic architecture and inheritance of human ribosomal RNA gene clusters.

Authors:  Dawn M Stults; Michael W Killen; Heather H Pierce; Andrew J Pierce
Journal:  Genome Res       Date:  2007-11-19       Impact factor: 9.043

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