Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13-q23
Journal Article
·
· Genomics; (United States)
- Creighton Univ. Medical School, Omaha, NE (United States)
- Colorado Univ. Health Sciences Center, Denver, CO (United States)
- Albert Einstein School of Medicine, Bronx, NY (United States)
At least two loci are known to exist for autosomal dominant polycystic kidney disease (ADPKD). One was localized to 16p, but the second less common locus has remained unlinked. Over 100 microsatellite markers, distributed across all chromosomes, have been typed on informative family members from the large Sicilian kindred in which the genetic heterogeneity was first discovered. Both the affected and the unaffected status of every family member used in the study were consulted in the successful localization of a second ADPKD gene to chromosome 4q. It was found to be flanked by the markers D4S231 and D4S414, defining a segment that spans about 9 cM. The new locus has been designated PKD4. This second localization will allow researchers to target another ADPKD gene for isolation in an effort to understand the pathogenesis of this common disorder. Furthermore, when flanking markers for the second ADPKD gene are used in conjunction with flanking markers for PKD1, the accuracy of the diagnosis of the subtype of ADPKD present in any particular family will be enhanced. This will improve the accuracy of linkage-based presymptomatic diagnoses by reducing the error due to genetic heterogeneity. 42 refs., 3 figs., 1 tab.
- OSTI ID:
- 7076739
- Journal Information:
- Genomics; (United States), Journal Name: Genomics; (United States) Vol. 18:3; ISSN GNMCEP; ISSN 0888-7543
- Country of Publication:
- United States
- Language:
- English
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