Literature DB >> 466852

Satellite DNA loss and nucleolar organiser activity in an individual with a de novo chromosome 13,14 translocation.

J R Gosden, C M Gosden, S S Lawrie, K E Buckton.   

Abstract

The distribution of satellite DNA and nucleolar organiser activity have been studied in a female with a new dicentric translocation chromosome derived from the maternal chromosomes 13 and 14. More than half the satellite DNA (60.5%) was lost in the translocation, together with both the nucleolar organiser regions (NOR'S). However, at least one NOR (chromosome 21) which was inactive in the mother (by the AgI reaction) is active in the subject, and this may be an example of functional compensation. The somatic cells of the mother of the subject, which do not have the translocation, show a high frequency of acrocentric associations, but these do not include any obvious excess of associations involving chromosomes 13 and 14, indicating that the high frequency of association in somatic cells is not in itself a predisposition to Robertsonian translocation in germ line cells. The father's chromosomes 9 both have more satellite DNA in the secondary constriction than normal, but this is not reflected in any obviously larger size of the C-band in this region.

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Year:  1979        PMID: 466852     DOI: 10.1111/j.1399-0004.1979.tb00836.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  11 in total

1.  Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation.

Authors:  F Pellestor; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

2.  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

3.  Molecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints.

Authors:  J Y Han; K H Choo; L G Shaffer
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

4.  Satellite DNA and cytological staining patterns in heterochromatic inversions of human chromosome 9.

Authors:  J R Gosden; G Spowart; S S Lawrie
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation.

Authors:  J M Varley; J Gosden; M Hultén
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  The identification of human chromosomes by quinacrine fluorescence after hybridisation in situ.

Authors:  S S Lawrie; J R Gosden
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  NORs and satellite associations in a family with 13/14 translocation.

Authors:  J Nikolis; V Kekić; V Diklić
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 8.  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

9.  Structural basis for Robertsonian translocations in man: association of ribosomal genes in the nucleolar fibrillar center in meiotic spermatocytes and oocytes.

Authors:  A Stahl; J M Luciani; M Hartung; M Devictor; J L Bergé-Lefranc; M Guichaoua
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

10.  The association of the nucleolus and the short arm of acrocentric chromosomes with the XY pair in human spermatocytes: its possible role in facilitating sex-chromosome acrocentric translocations.

Authors:  A Stahl; M Hartung; M Devictor; J L Bergé-Lefranc
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

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