dCAPS, a simple technique for the genetic analysis of single nucleotide polymorphisms: experimental applications in Arabidopsis thaliana genetics
- 1 May 1998
- journal article
- research article
- Published by Wiley in The Plant Journal
- Vol. 14 (3) , 387-392
- https://doi.org/10.1046/j.1365-313x.1998.00124.x
Abstract
Summary: PCR‐based detection of single nucleotide polymorphisms is a powerful tool for the plant geneticist. Cleaved amplified polymorphic sequence analysis is the most widely used approach for the detection of single nucleotide polymorphisms. However, this technique is limited to mutations which create or disrupt a restriction enzyme recognition site. This paper presents a modification of this technique where mismatches in a PCR primer are used to create a polymorphism based on the target mutation. This technique is useful for following known mutations in segregating populations and genetic mapping of isolated DNAs used for positional based cloning of new genes. In addition, a computer program has been developed that facilitates the design of these PCR primers.Keywords
This publication has 15 references indexed in Scilit:
- Genetic similarity among Arabidopsis thaliana ecotypes estimated by DNA sequence comparisonPlant Molecular Biology, 1996
- Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization.Genome Research, 1995
- Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphismsNucleic Acids Research, 1994
- Recombinant inbred lines for mapping RFLP and phenotypic markers in Arabidopsis thalianaThe Plant Journal, 1993
- A procedure for mapping Arabidopsis mutations using co‐dominant ecotype‐specific PCR‐based markersThe Plant Journal, 1993
- Single nucleotide primer extension to detect genetic diseases: experimental application to hemophilia B (factor IX) and cystic fibrosis genes.Proceedings of the National Academy of Sciences, 1991
- Genetic disease detection and DNA amplification using cloned thermostable ligase.Proceedings of the National Academy of Sciences, 1991
- Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)Nucleic Acids Research, 1989
- Modification of enzymatic-ally amplified DNA for the detection of point mutationsNucleic Acids Research, 1989
- Detection of single base substitutions in total genomic DNANature, 1985