Literature DB >> 1746561

Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizations.

R Feil1, P Aubourg, J Mosser, A M Douar, D Le Paslier, C Philippe, J L Mandel.   

Abstract

We have characterized a complex chromosomal rearrangement in band Xq28, in an adrenoleukodystrophy patient who also has blue-cone monochromacy. A 130-kb region upstream from the color-vision pigment genes was isolated as yeast artificial chromosome or cosmid clones. Another Xq28 sequence, not included in the above region, was obtained by cloning a deletion breakpoint from the patient. Using probes derived from the cloned sequences, we have shown that the rearrangement affects the color-pigment genes and includes two deletions, most likely separated by a large (greater than 110-kb) inversion. One deletion encompasses part of the pigment gene cluster and 33 kb of upstream sequences and accounts for the patient's blue-cone monochromacy. If this rearrangement also caused ALD, the disease gene would be expected to lie within or close to one of the deletions. However, deletions were not detected in a 50-kb region upstream of the red-color-pigment gene in 81 other ALD patients. Two CpG islands were mapped, at 46 and 115 kb upstream from the pigment genes.

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Year:  1991        PMID: 1746561      PMCID: PMC1686466     

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


  35 in total

1.  Adrenoleucodystrophy: a molecular genetic study in five families.

Authors:  R G Del Mastro; S Bundey; M W Kilpatrick
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

Review 2.  Report of the committee on the genetic constitution of the X chromosome.

Authors:  K E Davies; J L Mandel; A P Monaco; R L Nussbaum; H F Willard
Journal:  Cytogenet Cell Genet       Date:  1990

3.  Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries.

Authors:  D Nizetić; G Zehetner; A P Monaco; L Gellen; B D Young; H Lehrach
Journal:  Proc Natl Acad Sci U S A       Date:  1991-04-15       Impact factor: 11.205

4.  Deficiency in red blood cells.

Authors:  D MacDonald; M Town; P Mason; T Vulliamy; L Luzzatto; D K Goff
Journal:  Nature       Date:  1991-03-14       Impact factor: 49.962

5.  Megabase inversions in the human genome as physiological events.

Authors:  G M Weichhold; H G Klobeck; R Ohnheiser; G Combriato; H G Zachau
Journal:  Nature       Date:  1990-09-06       Impact factor: 49.962

6.  Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

Authors:  B A van Oost; P M van Zandvoort; W Tünte; H G Brunner; A J Hoogeboom; P D Maaswinkel-Mooy; J Bakkeren; B Hamel; H H Ropers
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

7.  Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.

Authors:  H M Albertsen; H Abderrahim; H M Cann; J Dausset; D Le Paslier; D Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

8.  Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.

Authors:  W T Brown; A C Gross; P Goonewardena; C Ferrando; C Dobkin; E C Jenkins
Journal:  Am J Med Genet       Date:  1991 Feb-Mar

9.  DNA inversion within the apolipoproteins AI/CIII/AIV-encoding gene cluster of certain patients with premature atherosclerosis.

Authors:  S K Karathanasis; E Ferris; I A Haddad
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

10.  Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei.

Authors:  B J Trask; H Massa; S Kenwrick; J Gitschier
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

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  9 in total

1.  Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

Authors:  I Bach; D Robinson; N Thomas; H H Ropers; F P Cremers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3).

Authors:  I Bach; H G Brunner; P Beighton; R H Ruvalcaba; W Reardon; M E Pembrey; S D van der Velde-Visser; G A Bruns; C W Cremers; F P Cremers
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

3.  A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Authors:  R Fujita; E Bingham; P Forsythe; C McHenry; V Aita; B A Navia; K Dry; M Segal; M Devoto; G Bruns; A F Wright; J Ott; P A Sieving; A Swaroop
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

4.  X-linked adrenoleukodystrophy and haemophilia A in the same kindred.

Authors:  A Nogueira; P Jorge; J Dores; M Cunha; S Sousa; I Pereira; M Campos; B Justiça; D Quelhas; M Sá Miranda
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

5.  Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Authors:  G H Sack; M Alpern; T Webster; R P Feil; J C Morrell; G Chen; W Chen; C T Caskey; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

Review 6.  DNA diagnosis of X-linked adrenoleukodystrophy.

Authors:  S Seneca; W Lissens
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

7.  Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.

Authors:  B Fournier; J M Saudubray; B Benichou; S Lyonnet; A Munnich; H Clevers; B T Poll-The
Journal:  J Clin Invest       Date:  1994-08       Impact factor: 14.808

8.  Chromosomal rearrangement segregating with adrenoleukodystrophy: associated changes in color vision.

Authors:  M Alpern; G H Sack; D H Krantz; J Jenness; H Zhang; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

9.  The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.

Authors:  Bernd Wissinger; Britta Baumann; Elena Buena-Atienza; Zeinab Ravesh; Artur V Cideciyan; Katarina Stingl; Isabelle Audo; Isabelle Meunier; Beatrice Bocquet; Elias I Traboulsi; Alison J Hardcastle; Jessica C Gardner; Michel Michaelides; Kari E Branham; Thomas Rosenberg; Sten Andreasson; Hélène Dollfus; David Birch; Andrea L Vincent; Loreto Martorell; Jaume Català Mora; Ulrich Kellner; Klaus Rüther; Birgit Lorenz; Markus N Preising; Emanuela Manfredini; Yuri A Zarate; Raymon Vijzelaar; Eberhart Zrenner; Samuel G Jacobson; Susanne Kohl
Journal:  Proc Natl Acad Sci U S A       Date:  2022-06-27       Impact factor: 12.779

  9 in total

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