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The major site for mutations leading to autosomal dominant polycystic kidney disease (ADPKD) is at the PKD1 locus, previously mapped to 16p13. Three additional probes have now been mapped within an existing array of genetic markers flanking this locus. One of these, CMM65b (D16S84), shows no recombination with PKD1 in 201 informative meioses. The others, Fr3-42 (D16S21) and EKMDA2 (D16S83), are shown to be the closest telomeric flanking markers. Somatic cell hybrids containing derivative chromosome 16s were used to construct a physical map of the region. Cosmid overlap cloning of the D16S84 region allowed a t(16;1) translocation breakpoint to be mapped at the molecular level, orientating the extended D16S84 locus with respect to the chromosome. The new markers and physical map described here provide an improved framework for attempts to clone the PKD1 region and to identify polycystic kidney disease mutations.

Type

Journal article

Journal

American journal of human genetics

Publication Date

05/1990

Volume

46

Pages

925 - 933

Addresses

Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510.

Keywords

Hybrid Cells, Chromosomes, Human, Pair 16, Animals, Humans, Mice, Polycystic Kidney Diseases, Globins, DNA Probes, Chromosome Mapping, Restriction Mapping, Meiosis, Recombination, Genetic, Genes, Dominant, Europe, Newfoundland and Labrador, Genetic Linkage