Is the frameshift codons 8/9 (+G) [FSC 8/9 (+G)] ?-thalassemia mutation, detected by the polymerase chain reaction-amplification refractory mutation system, really FSC 8/9 (+G)?
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Abstract
There are several polymerase chain reaction (PCR)-based approaches for the analysis of known mutations. The PCR-amplification refractory mutation system (PCR-ARMS) is one of the best known and frequently used for the detection of ?-thalassemia (?-thal) mutations. However, there is an important point to be considered when searching for the frameshift codon (FSC) 8 (-AA) and FSC 8/9 (+G) mutations. Whereas the primer is specific for the FSC 8 mutation only, the primer for the FSC 8/9 mutation does not discriminate between the FSC 8/9 and FSC 8 mutations. Thus, the high number of FSC8/9 mutations reported in countries like India, Pakistan and some regions of Iran may be due to the use of the FSC 8/9 primer, without taking the FSC 8 mutation into account. It is thus advisable to test for FSC 8 before the FSC 8/9 mutation whenever PCR-ARMS is the method of investigation for these two mutations. Copyright é Informa Healthcare USA, Inc.
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DNA, article, Asian, beta thalassemia, codon, ethnic group, frameshift mutation, gene amplification, gene mutation, human, India, Indian, Iran, Pakistan, polymerase chain reaction, polymerase chain reaction amplification refractory mutation system, population genetics, beta-Thalassemia, Codon, DNA Primers, Frameshift Mutation, Humans, Polymerase Chain Reaction, Reproducibility of Results, Sensitivity and Specificity