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Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizations.
Feil, R; Aubourg, P; Mosser, J; Douar, A M; Le Paslier, D; Philippe, C; Mandel, J L.
Afiliación
  • Feil R; Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Strasbourg, France.
Am J Hum Genet ; 49(6): 1361-71, 1991 Dec.
Article en En | MEDLINE | ID: mdl-1746561
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pigmentos Retinianos / Cromosoma X / Defectos de la Visión Cromática / Aberraciones Cromosómicas / Adrenoleucodistrofia Límite: Humans / Male Idioma: En Revista: Am J Hum Genet Año: 1991 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pigmentos Retinianos / Cromosoma X / Defectos de la Visión Cromática / Aberraciones Cromosómicas / Adrenoleucodistrofia Límite: Humans / Male Idioma: En Revista: Am J Hum Genet Año: 1991 Tipo del documento: Article País de afiliación: Francia