Literature DB >> 868876

The origin and behavior of two isodicentric bisatellited chromosomes.

D L Van Dyke, L Weiss, M Logan, G S Pai.   

Abstract

Karyotyping revealed three cell lines in a boy with mental retardation and few other abnormalities. Thirty cells exhibited a normal karyotype, and 54 had an extra acrocentric chromosome of E group size with satellites on the long and short arms. The remaining 20 cells each had, in addition to the first marker (M1), a second tiny bisatellited chromosome (M2). C-banding demonstrated that both markers were dicentric. G-, C-, and Q-banding and satellite association data were consistent with the markers having originated from chromosome 15 material. We propose that M1 was formed from a meiotic breakage and a chromatid fusion in the proximal long arms of an acrocentric pair. This would have produced a symmetrical isodicentric chromosomes, plus one or two acentric fragments. M2 then could have resulted from a dicentric bridge-break-synthesis-reunion phenomenon. This model of abnormal meiotic exchange can be generalized to encompass the formation of other dicentric isochromosome cases of isochromosome X.

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Year:  1977        PMID: 868876      PMCID: PMC1685319     

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


  26 in total

1.  Chromosomal translocations in mongolism and in normal relatives.

Authors:  L S PENROSE; J R ELLIS; J D DELHANTY
Journal:  Lancet       Date:  1960-08-20       Impact factor: 79.321

2.  Dicentric human X chromosomes.

Authors:  A De la Chapelle; K Stenstrand
Journal:  Hereditas       Date:  1974       Impact factor: 3.271

3.  Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.

Authors:  S Kakati; A K Sinha
Journal:  Hum Hered       Date:  1973-04       Impact factor: 0.444

4.  Apparently isodicentric but functionally monocentric X chromosome in man.

Authors:  E Therman; G E Sarto; K Patau
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

5.  Multiple anomalies associated with an extra small metacentric chromosome: modified Giemsa stain results.

Authors:  W Tangheroni; A Cao; M Furbetta
Journal:  Humangenetik       Date:  1973

6.  New staining methods for chromosomes.

Authors:  H A Lubs; W H McKenzie; S R Patil; S Merrick
Journal:  Methods Cell Biol       Date:  1973       Impact factor: 1.441

7.  Partial trisomy of chromosome 15.

Authors:  C E Parker; O S Alfi
Journal:  Lancet       Date:  1972-05-13       Impact factor: 79.321

8.  An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.

Authors:  C Distèche; A Hagemeijer; J Frederic; D Progneaux
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

9.  Partial trisomy 15.

Authors:  R E Magenis; K M Overton; J A Reiss; J P Macfarlane; F Hecht
Journal:  Lancet       Date:  1972-12-23       Impact factor: 79.321

10.  A masculinizing syndrome associated with a doubly-satellited extra chromosome.

Authors:  R A Rohde
Journal:  J Med Genet       Date:  1965-12       Impact factor: 6.318

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  17 in total

1.  Infertility associated with two accessory bisatellited chromosomes.

Authors:  M A Martín-Lucas; A Pérez-Castillo; J A Abrisqueta
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

2.  Forty four probands with an additional "marker" chromosome.

Authors:  K E Buckton; G Spowart; M S Newton; H J Evans
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 3.  Inv dup(15) supernumerary marker chromosomes.

Authors:  T Webb
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

4.  Cat eye syndrome owing to tetrasomy 22pter leads to q11.

Authors:  G N Wilson; D L Baker; J Schau; J Parker
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

5.  Dicentric chromosome 13 and centromere inactivation.

Authors:  S Schwartz; C G Palmer; D D Weaver; J Priest
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Cytogenetic and clinical studies in five cases of inv dup(15).

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

Review 7.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.

Authors:  Jung Min Ko; Jun Bum Kim; Ki Soo Pai; Jun-No Yun; Sang-Jin Park
Journal:  J Korean Med Sci       Date:  2010-11-24       Impact factor: 2.153

9.  Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

Authors:  S E Roberts; F Maggouta; N S Thomas; P A Jacobs; J A Crolla
Journal:  Am J Hum Genet       Date:  2003-10-14       Impact factor: 11.025

Review 10.  Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements.

Authors:  Martin Poot; Thomas Haaf
Journal:  Mol Syndromol       Date:  2015-08-15
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