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Karyotypic abnormality of the X chromosome is rare in mutant HPRT-lymphocyte clones.
Muir, P; Osborne, Y; Morley, A A; Turner, D R.
Afiliación
  • Muir P; Department of Haematology, Flinders Medical Centre, Bedford Park, South Australia.
Mutat Res ; 197(1): 157-60, 1988 Jan.
Article en En | MEDLINE | ID: mdl-3336373
ABSTRACT
Lymphocyte clones mutated at the hypoxanthine-guanine phosphoribosyl-transferase (HPRT) locus on the X chromosome were studied by synchronization and G banding to determine the proportion of mutant clones having visible karyotypic change. 47 spontaneously mutant clones, 17 mutant clones induced by X-irradiation and 33 wild-type clones were studied. All clones were karyotypically normal except for 1 clone induced by X-irradiation in which an interstitial deletion of the short arm of the X chromosome had been inserted into the long arm of the same chromosome between q23 and q24; this change may have been coincidental or may have resulted in a position effect mutation. It was concluded that the great majority of mutations were not associated with a visible chromosome abnormality. This conclusion complements molecular studies which suggest that gene changes at the HPRT locus in HPRT- mutants generally extend over segments of DNA too small to be resolved by karyotypic analysis.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas Sexuales / Cromosoma X / Linfocitos / Hipoxantina Fosforribosiltransferasa / Mutación Límite: Humans Idioma: En Revista: Mutat Res Año: 1988 Tipo del documento: Article
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aberraciones Cromosómicas Sexuales / Cromosoma X / Linfocitos / Hipoxantina Fosforribosiltransferasa / Mutación Límite: Humans Idioma: En Revista: Mutat Res Año: 1988 Tipo del documento: Article