How sensitive is PCR-SSCP?
- 1 January 1993
- journal article
- review article
- Published by Hindawi Limited in Human Mutation
- Vol. 2 (5), 338-346
- https://doi.org/10.1002/humu.1380020503
Abstract
Single-strand conformation polymorphism analysis (SSCP) is a rapid method for detection of minor sequence changes in polymerase chain reaction-amplified DNA. Since the first reported use of SSCP in 1989 (Orita et al., 1989), this technique has been used widely to detect mutations in oncogenes, tumor suppressor genes, and genes responsible for genetic diseases. Published mutations that have been detected using this technique include base substitutions, small insertions and deletions, and rearrangements. This technique has also been applied for the detection of DNA polymorphisms at various loci of the human genome (reviewed by Hayashi, 1991; Hayashi, 1993). However, many factors can influence the sensitivity of SSCP, and its optimization is highly empirical. In this review, we estimate the percentage of mutations that can be detected by this technique under various controlled conditions, and describe some critical elements affecting sensitivity.Keywords
This publication has 34 references indexed in Scilit:
- Detection of point mutations in the p53 gene: Comparison of single-strand conformation polymorphism, constant denaturant gel electrophoresis, and hydroxylamine and osmium tetroxide techniquesHuman Mutation, 1993
- F-SSCP: fluorescence-based polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) analysis.Genome Research, 1992
- PCR-SSCP: A method for detection of mutationsGenetic Analysis: Biomolecular Engineering, 1992
- Detection of point mutations in human DNA by analysis of RNA conformation polymorphism(s)Nucleic Acids Research, 1992
- PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA.Genome Research, 1991
- Diagnostic single strand conformational polymorphism, (SSCP): a simplified non-radioisotopic method as applied to a Tay-Sachs B1 variantNucleic Acids Research, 1991
- A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutationsCell, 1990
- Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.Proceedings of the National Academy of Sciences, 1988
- Separation of random fragments of DNA according to properties of their sequences.Proceedings of the National Academy of Sciences, 1980
- Polyacrylamide Gel ElectrophoresisScience, 1971