Literature DB >> 323137

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15.

R R Schreck, W R Breg, B F Erlanger, O J Miller.   

Abstract

The marked binding of antibodies specific for 5-methylcytidine to the short arm of chromosome 15 distinguishes this chromosome from the other human acrocentrics. This method has been used to study over 60 individuals including 12 who did not have Down's syndrome, but who did have an extra G-group sized acrocentric chromosome. In six cases the extra chromosome did not show intensive binding of anti-5-methylcytidine. In the other six cases, the extra chromosome contained a 5-methylcytidine rich band at each end indicating that both ends were derived from chromosome 15 and contained centromeric heterochromatin normally present on the short arm of chromosome 15. The duplication of short arm material in the abnormal chromosomes was confirmed in all cases by quinacrine staining, nucleolar organizer (Ag-AS) staining or C-banding. In three cases, the abnormal chromosome appeared to arise from two different chromosomes 15. Several possible mechanisms for the production of the abnormal chromosome are discussed. The individuals with this abnormal chromosome all showed some degree of mental retardation, but few common physical findings.

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Year:  1977        PMID: 323137     DOI: 10.1007/bf00390430

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


  14 in total

Review 1.  Immunochemical probes of human chromosome organization.

Authors:  O J Miller; B F Erlanger
Journal:  Pathobiol Annu       Date:  1975

2.  ANTIBODIES SPECIFIC FOR RIBONUCLEOSIDES AND RIBONUCLEOTIDES AND THEIR REACTION WITH DNA.

Authors:  B F ERLANGER; S M BEISER
Journal:  Proc Natl Acad Sci U S A       Date:  1964-07       Impact factor: 11.205

3.  5-Methylcytosine localised in mammalian constitutive heterochromatin.

Authors:  O J Miller; W Schnedl; J Allen; B F Erlanger
Journal:  Nature       Date:  1974-10-18       Impact factor: 49.962

4.  Distinctive fluorescence of quinacrine-labelled human G group chromosomes.

Authors:  W R Breg; O J Miller; D A Miller; P W Allderdice
Journal:  Nat New Biol       Date:  1971-06-30

5.  Palindromic base sequences and replication of eukaryote chromosome ends.

Authors:  T Cavalier-Smith
Journal:  Nature       Date:  1974-08-09       Impact factor: 49.962

6.  A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres.

Authors:  D Warburton; A S Henderson; L R Shapiro; L Y Hsu
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

7.  Differential staining of the satellite regions of human acrocentric chromosomes.

Authors:  W M Howell; T E Denton; J R Diamond
Journal:  Experientia       Date:  1975-02-15

8.  Visualization of nucleolar organizer regions im mammalian chromosomes using silver staining.

Authors:  C Goodpasture; S E Bloom
Journal:  Chromosoma       Date:  1975-11-20       Impact factor: 4.316

9.  Serologic specificities of methylated base immune systems.

Authors:  L Levine; H Van Vunakis; R C Gallo
Journal:  Biochemistry       Date:  1971-05-25       Impact factor: 3.162

10.  Identification of the mouse karyotype by quinacrine fluorescence, and tentative assignment of seven linkage groups.

Authors:  O J Miller; D A Miller; R E Kouri; P W Allderdice; V G Dev; M S Grewal; J J Hutton
Journal:  Proc Natl Acad Sci U S A       Date:  1971-07       Impact factor: 11.205

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  38 in total

1.  Bivalent 15 regularly associates with the sex vesicle in normal male meiosis.

Authors:  C Metzler-Guillemain; C Mignon; D Depetris; M R Guichaoua; M G Mattei
Journal:  Chromosome Res       Date:  1999       Impact factor: 5.239

2.  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

3.  The structural organization of mouse metaphase chromosomes.

Authors:  R R Schreck; V G Dev; B F Erlanger; O J Miller
Journal:  Chromosoma       Date:  1977-07-18       Impact factor: 4.316

4.  Maternal origin of inv dup(15) chromosomes in infantile autism.

Authors:  T Martinsson; T Johannesson; M Vujic; A Sjöstedt; S Steffenburg; C Gillberg; J Wahlström
Journal:  Eur Child Adolesc Psychiatry       Date:  1996-12       Impact factor: 4.785

5.  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 6.  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

7.  Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.

Authors:  L P Wisniewski; R A Doherty
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

Authors:  E Blennow; H Telenius; D de Vos; C Larsson; P Henriksson; O Johansson; N P Carter; M Nordenskjöld
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

9.  Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

Authors:  J Leana-Cox; L Jenkins; C G Palmer; R Plattner; L Sheppard; W L Flejter; J Zackowski; F Tsien; S Schwartz
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

10.  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

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