Literature DB >> 8477265

Detection of point mutations in the p53 gene: comparison of single-strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniques.

A Condie1, R Eeles, A L Borresen, C Coles, C Cooper, J Prosser.   

Abstract

A comparison was made between the 3 most commonly used techniques for the detection of point mutations: single-strand conformation polymorphism (SSCP), constant denaturant gel electrophoresis (CDGE), and hydroxylamine and osmium tetroxide used in amplification mismatch cleavage analysis (HOT). Using human DNA samples containing known mutations in the p53 gene, SSCP detected 90% of mutations (18/20), CDGE detected 88% (15/17) pre-decoding of the samples but 100% when the mutations were known and the CDGE conditions optimized, and the HOT technique was 100% accurate, although 1 mutation was missed through careless examination of the gel. The positive and negative aspects of each of the techniques are considered and suggestions are made regarding the particular situations in which each of them is most useful.

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Year:  1993        PMID: 8477265     DOI: 10.1002/humu.1380020111

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  17 in total

1.  The genetic epidemiology of early-onset epithelial ovarian cancer: a population-based study.

Authors:  J F Stratton; D Thompson; L Bobrow; N Dalal; M Gore; D T Bishop; I Scott; G Evans; P Daly; D F Easton; B A Ponder
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  Specific intronic p53 mutation in esophageal squamous cell carcinoma in Southern Thailand.

Authors:  Paramee Thongsuksai; Pleumjit Boonyaphiphat; Puttisak Puttawibul; Wanna Sudhikaran
Journal:  World J Gastroenterol       Date:  2010-11-14       Impact factor: 5.742

3.  p53 gene alterations and protein accumulation in colorectal cancer.

Authors:  R Bertorelle; G Esposito; C Belluco; L Bonaldi; A Del Mistro; D Nitti; M Lise; L Chieco-Bianchi
Journal:  Clin Mol Pathol       Date:  1996-04

Review 4.  Gene-based approach to human gene-phenotype correlations.

Authors:  T P Dryja
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

5.  Diverse mutations in patients with Menkes disease often lead to exon skipping.

Authors:  S Das; B Levinson; S Whitney; C Vulpe; S Packman; J Gitschier
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

6.  TP53 alterations in atypical ductal hyperplasia and ductal carcinoma in situ of the breast.

Authors:  M Chitemerere; T I Andersen; R Holm; F Karlsen; A L Børresen; J M Nesland
Journal:  Breast Cancer Res Treat       Date:  1996       Impact factor: 4.872

7.  Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin gene.

Authors:  U Lenk; R Hanke; U Kräft; K Grade; I Grunewald; A Speer
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

8.  Inheritance and molecular variations of PCR-SSCP fragments in pedunculate oak (Quercus robur L.).

Authors:  C Bodenes; A Kremer; F Laigret
Journal:  Theor Appl Genet       Date:  1996-08       Impact factor: 5.699

9.  Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

Authors:  C Eng; V Murday; S Seal; S Mohammed; S V Hodgson; M A Chaudary; I S Fentiman; B A Ponder; R A Eeles
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

10.  Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor gene.

Authors:  R Whittall; V Gudnason; G P Weavind; L B Day; S E Humphries; I N Day
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

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