Literature DB >> 640652

The fate of DNA satellites I, II, III and ribosomal DNA in a familial dicentric chromosome 13:14.

J R Gosden, C Gosden, S Lawrie, A R Mitchell.   

Abstract

In a family with a stable dicentric 13:14 translocation chromosome, the distribution of DNA sequences complementary to satellite DNAs I, II and III and ribosomal RNA were studied. The translocation chromosome showed a loss of sequences complementary to all three satellite DNAs, located in the short arms of the acrocentric chromosomes, but slightly more of the sequences complementary to satellite I were retained than of the other two satellite DNAs. The fact that material was lost from all three satellites indicates that they are not present as single discrete blocks in these chromosomes, when we would expect to find the distal sequences lost and the proximal ones retained, but consist of interspersed blocks with each sequence represented by more than one, and probably several blocks. There was a total loss of ribosomal DNA from the nucleolar organiser regions of the chromosomes involved in the 13:14 translocation, but an interesting finding was the presence of extra ribosomal DNA and satellite DNAs I, II and III in one chromosome 22 which was found in seven out of nine individuals of the family with the 13:14 translocation, and in only one of five individuals without the translocation. There may be a compensatory mechanism present when certain sequences are elminated during chromosomal rearrangements. The relationship of such mechanisms to reproductive fitness is discussed.

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Year:  1978        PMID: 640652     DOI: 10.1007/BF00273095

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


  30 in total

1.  Characterisation of DNA from condensed and dispersed human chromatin.

Authors:  J R Gosden; A R Mitchell
Journal:  Exp Cell Res       Date:  1975-04       Impact factor: 3.905

2.  ABSENCE OF RIBOSOMAL RNA SYNTHESIS IN THE ANUCLEOLATE MUTANT OF XENOPUS LAEVIS.

Authors:  D D BROWN; J B GURDON
Journal:  Proc Natl Acad Sci U S A       Date:  1964-01       Impact factor: 11.205

3.  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

4.  Association of D/D translocations with fetal wastage and aneuploidy. A report of four families.

Authors:  P M Fernhoff; D N Singh; J Hanson; S Trusler; C R Dumont; A T Chen
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

5.  Incidence and mutation rates of structural rearrangements of the autosomes in man.

Authors:  P A Jacobs; A Frackiewicz; P Law
Journal:  Ann Hum Genet       Date:  1972-03       Impact factor: 1.670

6.  Reciprocal translocation versus centric fusion between two No. 13 chromosomes. A case of 46,XX,-13,+t(13;13)(p12;q13) and a case of 46,XY,-13,+t(13;13)(p12;p12).

Authors:  L Y Hsu; H J Kim; E Sujansky; B Kousseff; K Hirschhorn
Journal:  Cytogenet Cell Genet       Date:  1973

7.  Fusion of homologous chromosomes (15q15q) as cause of recurrent abortion.

Authors:  M Bartsch-Sandhoff
Journal:  Lancet       Date:  1977-03-05       Impact factor: 79.321

8.  Incidence of chromosome aberrations among 11148 newborn children.

Authors:  J Nielsen; I Sillesen
Journal:  Humangenetik       Date:  1975-10-20

9.  Patterns of silver staining of human chromosomes.

Authors:  J M Varley
Journal:  Chromosoma       Date:  1977-05-23       Impact factor: 4.316

10.  The distribution of sequences complementary to human satellite DNAs I, II and IV in the chromosomes of chimpanzee (Pan troglodytes), gorilla (Gorilla gorilla) and orang utan (Pongo pygmaeus).

Authors:  J R Gosden; A R Mitchell; H N Seuanez; C M Gosden
Journal:  Chromosoma       Date:  1977-09-27       Impact factor: 4.316

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  9 in total

1.  Homologous subfamilies of human alphoid repetitive DNA on different nucleolus organizing chromosomes.

Authors:  A L Jørgensen; C J Bostock; A L Bak
Journal:  Proc Natl Acad Sci U S A       Date:  1987-02       Impact factor: 11.205

Review 2.  Satellite DNA and heterochromatin variants: the case for unequal mitotic crossing over.

Authors:  D M Kurnit
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

3.  Assignment of human satellite 1 DNA as revealed by fluorescent in situ hybridization with oligonucleotides.

Authors:  I Tagarro; J Wiegant; A K Raap; J J González-Aguilera; A M Fernández-Peralta
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

4.  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

5.  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

6.  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

7.  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

8.  Intercalar satellites of human acrocentric chromosomes as a cytological manifestation of polymorphism in GC-rich material?

Authors:  P Balícek; J Zizka
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

9.  Amniotic fluid cell morphology in early antenatal prediction of abortion and low birth weight.

Authors:  C Gosden; D J Brock
Journal:  Br Med J       Date:  1978-10-28
  9 in total

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