Literature DB >> 1384329

A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

L L Estabrooks1, A N Lamb, H N Kirkman, N P Callanan, K W Rao.   

Abstract

We report two families with a satellited chromosome 4 short arm (4ps). Satellites and stalks normally occur on the short arms of acrocentric chromosomes; however, the literature cites several reports of satellited nonacrocentric chromosomes, which presumably result from a translocation with an acrocentric chromosome. This is the first report of 4ps chromosomes. Our families are remarkable in that both unaffected and affected individuals carry the 4ps chromosome. The phenotypes observed in affected individuals, although dissimilar, were sufficient to encourage a search for a deletion of chromosome 4p. By Southern blot analysis and fluorescence in situ hybridization, a deletion of material mapping approximately 150 kb from chromosome 4pter was discovered. This deletion is notable because it does not result in the Wolf-Hirschhorn syndrome and can result in an apparently normal phenotype. We speculate that homology between subterminal repeat sequences on 4p and sequences on the acrocentric short arms may explain the origin of the rearrangement and that position effect may play a role in the expression of the abnormal phenotype.

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Year:  1992        PMID: 1384329      PMCID: PMC1682839     

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


  24 in total

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Authors:  J C Murray; G B van Ommen
Journal:  Cytogenet Cell Genet       Date:  1990

2.  Nucleolus organizer regions (NORs) inserted in 6q15.

Authors:  F Prieto; L Badía; M Beneyto; F Palau
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

3.  Clonal inheritance of rRNA gene activity: cytological evidence in human cells.

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Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

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

5.  A familial insertion involving an active nucleolar organiser within chromosome 12.

Authors:  J L Watt; D A Couzin; D J Lloyd; G S Stephen; E McKay
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

6.  The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomere.

Authors:  N A Doggett; J F Cheng; C L Smith; C R Cantor
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

7.  Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.

Authors:  C Verellen-Dumoulin; M Freund; R De Meyer; C Laterre; J Frédéric; M W Thompson; V D Markovic; R G Worton
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].

Authors:  M G Wilson; J W Towner; G S Coffin; A J Ebbin; E Siris; P Brager
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Translocation of the nucleolus organizer region to the human X chromosome.

Authors:  G Stetten; B Sroka; M Schmidt; J Axelman; B R Migeon
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

10.  Correlation of differentiation state and silver staining of nucleolar organizers in the promyelocytic leukemia cell line HL-60.

Authors:  B R Reeves; G Casey; J R Honeycombe; S Smith
Journal:  Cancer Genet Cytogenet       Date:  1984-10
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  4 in total

1.  Two sibs with Wolf-Hirschhorn and DiGeorge deletions resulting from an unbalanced chromosome rearrangement, 45,XX/XY, der(4)t(4;22) (p16.3;q11.2) mat,-22.

Authors:  K S Reddy; V Sulcova; B Siassi
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

2.  Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Authors:  L L Estabrooks; A N Lamb; A S Aylsworth; N P Callanan; K W Rao
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

3.  A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.

Authors:  C L Lin; L Gibson; B Pober; T L Yang-Feng
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

4.  AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development.

Authors:  Emmanuelle Bitoun; Mattéa J Finelli; Peter L Oliver; Sheena Lee; Kay E Davies
Journal:  J Neurosci       Date:  2009-12-09       Impact factor: 6.167

  4 in total

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