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Characterization of a YAC containing part or all of the Norrie disease locus.
- Source :
-
Human molecular genetics [Hum Mol Genet] 1992 Jun; Vol. 1 (3), pp. 161-4. - Publication Year :
- 1992
-
Abstract
- It has been shown from pulsed-field gel electrophoresis (PFGE) that the monoamine oxidase genes A and B (MAOA & MAOB) and DXS7 loci are physically very close. We have therefore extended studies on their relationship through the characterisation of a 650 kb YAC isolated using L1.28 (recognising the DXS7 locus) as a probe. Restriction mapping of the YAC indicates that it contains both MAOA and MAOB genes in addition to the DXS7 locus. The map derived from the YL1.28-YAC is compatible both with the map from an independently derived YAC carrying MAOA and B genes and with the long range genomic map for the region. A series of subclones prepared from a 'phage library (lambda DASH II) of the YAC have been characterised and have been employed to determine the end point of the deletion of a Norrie disease (NDP) patient who has been shown to lack both DXS7 and MAO coding sequences. The pattern of retention of subclones in the deletion patient place the end point of the deletion within 30-130 kb of the proximal end of the YAC. By combining the data with established recombination analysis, we provide evidence that all or part of the NDP lies in the interval of approximately 250kb within the YAC.
- Subjects :
- Blindness enzymology
Chromosome Deletion
Chromosome Mapping
Chromosomes, Fungal
DNA genetics
DNA Probes
Deafness enzymology
Deafness genetics
Gene Library
Genetic Markers
Genome, Human
Humans
Intellectual Disability enzymology
Intellectual Disability genetics
Monoamine Oxidase genetics
X Chromosome
Blindness genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0964-6906
- Volume :
- 1
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Human molecular genetics
- Publication Type :
- Academic Journal
- Accession number :
- 1303171
- Full Text :
- https://doi.org/10.1093/hmg/1.3.161