Literature DB >> 12080393

A cautionary note: false homozygosity for BRCA2 6174delT mutation resulting from a single nucleotide polymorphism masking the wt allele.

Angela R Solano1, Ricardo J Dourisboure, Jeffrey Weitzel, Ernesto J Podesta.   

Abstract

Sequencing an amplification product of the terminal segment of BRCA2 exon 11 showed apparent homozygosity for the 6174delT mutation in two healthy sisters. Subsequent sequencing of an alternate overlapping amplicon revealed the presence of the 5972C >T polymorphism, which is within the standard upstream amplification primer. This mismatch was responsible for the failure to amplify the normal (5972T) allele in both sisters who were heterozygous for the 6174delT mutation. Though the unexpected finding of apparent homozygosity for the 6174delT mutation prompted re-evaluation of the assay, the potential for false negative results due to masking of a mutation-bearing allele by such a circumstance should be a cautionary note for the testing and also in the interpretation of the results published under such assay conditions.

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Year:  2002        PMID: 12080393     DOI: 10.1038/sj.ejhg.5200821

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  5 in total

1.  Genetic screening for von Hippel-Lindau gene mutations in non-syndromic pheochromocytoma: low prevalence and false-positives or misdiagnosis indicate a need for caution.

Authors:  G Eisenhofer; C D Vocke; A Elkahloun; T-T Huynh; T Prodanov; J W M Lenders; H J Timmers; J N Benhammou; W M Linehan; K Pacak
Journal:  Horm Metab Res       Date:  2012-03-21       Impact factor: 2.936

2.  Identification of a novel single nucleotide polymorphism of HADHA gene at a referred primer-binding site during pre-diagnostic tests for preimplantation genetic diagnosis.

Authors:  Hyoung-Song Lee; Hye Won Choi; Chun Kyu Lim; Mi Kyoung Koong; Inn Soo Kang; Han-Wook Yoo; Jin-Ho Choi; Jin Hyun Jun
Journal:  J Korean Med Sci       Date:  2006-10       Impact factor: 2.153

3.  A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.

Authors:  Heather L Hondow; Stephen B Fox; Gillian Mitchell; Rodney J Scott; Victoria Beshay; Stephen Q Wong; Alexander Dobrovic
Journal:  BMC Cancer       Date:  2011-06-24       Impact factor: 4.430

4.  Rapid detection of carriers with BRCA1 and BRCA2 mutations using high resolution melting analysis.

Authors:  Elena A Takano; Gillian Mitchell; Stephen B Fox; Alexander Dobrovic
Journal:  BMC Cancer       Date:  2008-02-25       Impact factor: 4.430

5.  BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin.

Authors:  Angela Rosaria Solano; Gitana Maria Aceto; Dreanina Delettieres; Serena Veschi; Maria Isabel Neuman; Eduardo Alonso; Sergio Chialina; Reinaldo Daniel Chacón; Mariani-Costantini Renato; Ernesto Jorge Podestá
Journal:  Springerplus       Date:  2012-09-25
  5 in total

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