Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations

Alessandro Cama, Raffaele Palmirotta, Maria Cristina Curia, Diana L. Esposito, Annalisa Ranieri, Ferdinando Ficari, Rosa Valanzano, Pasquale Battista, Andrea Modesti, Francesco Tonelli, Renato Mariani-Costantini

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19 Citations (Scopus)

Abstract

Germline mutations of the adenomatous polyposis coli (APC) gene tend to cluster in discrete regions. Some of these mutations occur frequently in familial adenomatous polyposis coli (FAP) patients, and strategies for genetic diagnosis of the disease should include simple methods for their detection. We studied a total of 48 FAP-affected or 'at-risk' members from 31 unrelated FAP pedigrees. Unrelated patients were analyzed using heteroduplex analysis on agarose minigels (HAAM) and multiplex allele-specific PCR. This novel strategy readily and reliably detected the three frequently occurring APC deletions at codons 1061, 1068, and 1309, allowing identification of mutant alleles in nine unrelated patients. A targeted mutational analysis, based on HAAM and amplification refractory mutation system (ARMS), allowed the rapid identification of 11 additional subjects with germline deletions, among relatives of the patients in whom mutations had been detected by multiplex PCR and HAAM. The use of two independent PCR-based tests, employing distinct sets of primers, reduces the possibility that artifacts occurring during DNA amplification may interfere with the diagnostic evaluation. The analysis of genotype-phenotype correlations provided evidence for heterogeneity with regard to the extent of colonic and extracolonic manifestations of the disease in subjects bearing identical mutations. However, the consistent association of the deletion at codon 1309 with more severe colonic disease than that observed in patients with mutations at codons 1061 and 1068, supports a correlation between mutation site and penetrance of FAP.

Original languageEnglish
Pages (from-to)144-152
Number of pages9
JournalHuman Mutation
Volume5
Issue number2
DOIs
Publication statusPublished - 1995

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Adenomatous Polyposis Coli
Multiplex Polymerase Chain Reaction
Genetic Association Studies
Heteroduplex Analysis
Mutation
Codon
Sepharose
Alleles
Colonic Diseases
APC Genes
Polymerase Chain Reaction
Inborn Genetic Diseases
Penetrance
Germ-Line Mutation
Pedigree
Artifacts
DNA

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Cama, A., Palmirotta, R., Curia, M. C., Esposito, D. L., Ranieri, A., Ficari, F., ... Mariani-Costantini, R. (1995). Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations. Human Mutation, 5(2), 144-152. https://doi.org/10.1002/humu.1380050208

Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations. / Cama, Alessandro; Palmirotta, Raffaele; Curia, Maria Cristina; Esposito, Diana L.; Ranieri, Annalisa; Ficari, Ferdinando; Valanzano, Rosa; Battista, Pasquale; Modesti, Andrea; Tonelli, Francesco; Mariani-Costantini, Renato.

In: Human Mutation, Vol. 5, No. 2, 1995, p. 144-152.

Research output: Contribution to journalArticle

Cama, A, Palmirotta, R, Curia, MC, Esposito, DL, Ranieri, A, Ficari, F, Valanzano, R, Battista, P, Modesti, A, Tonelli, F & Mariani-Costantini, R 1995, 'Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations', Human Mutation, vol. 5, no. 2, pp. 144-152. https://doi.org/10.1002/humu.1380050208
Cama A, Palmirotta R, Curia MC, Esposito DL, Ranieri A, Ficari F et al. Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations. Human Mutation. 1995;5(2):144-152. https://doi.org/10.1002/humu.1380050208
Cama, Alessandro ; Palmirotta, Raffaele ; Curia, Maria Cristina ; Esposito, Diana L. ; Ranieri, Annalisa ; Ficari, Ferdinando ; Valanzano, Rosa ; Battista, Pasquale ; Modesti, Andrea ; Tonelli, Francesco ; Mariani-Costantini, Renato. / Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutations. In: Human Mutation. 1995 ; Vol. 5, No. 2. pp. 144-152.
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