Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene reveals six novel mutations

B. Peral, J. L. San Millan, A. C.M. Ong, V. Gamble, C. J. Ward, C. Strong, P. C. Harris

Research output: Contribution to journalArticle

115 Scopus citations


Recently, the gene for the most common form of autosomal dominant polycystic kidney disease (ADPKD), PKD1 (polycystic kidney disease 1), has been fully characterized and shown to encode an integral membrane protein, polycystin, involved in cell-cell and/or cell-matrix interactions. Study of the PKD1 gene has been complicated because most of the gene lies in a genomic region reiterated several times elsewhere on the same chromosome, and consequently only seven mutations have been described so far. Here we report a systematic screen covering ~80% of the ~2.75 kb of translated transcript that is encoded by single-copy DNA. We have identified and characterized six novel mutations that, together with the previously described changes, amount to a detection rate of 10%-15% in the population studied. The newly described mutations are two deletions, an insertion of a T-nucleotide causing a frameshift, two single-base-pair substitutions resulting in premature stop codons, and a G→C transversion that may be a missense mutation. These results have important implications for genetic diagnosis of PKD1 because they indicate that the majority of mutations lie within the duplicated area, which is difficult to study. The regions of polycystin removed in each mutation so far described are assessed for their functional significance; an area disrupted by two new small in-frame changes is highlighted. PKD1 mutations are contrasted with those in the PKD1/TSC2 contiguous-gene syndrome, and the likely mutational mechanism in PKD1 is considered.

Original languageEnglish (US)
Pages (from-to)86-96
Number of pages11
JournalAmerican journal of human genetics
Issue number1
StatePublished - 1996

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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