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Annealing control primer system for improving specificity of PCR amplification
Author(s) -
In Taek Hwang,
Yun-Jee Kim,
SeungHyun Kim,
Chae-Il Kwak,
Young-Yun Gu,
Jong-Yoon Chun
Publication year - 2003
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/03356st03
Subject(s) - linker , primer dimer , primer (cosmetics) , biology , oligonucleotide , polymerase chain reaction , nucleic acid sequence , microbiology and biotechnology , genotyping , duplex (building) , dna , genetics , computational biology , chemistry , gene , genotype , multiplex polymerase chain reaction , computer science , organic chemistry , operating system
A novel primer designed to improve the specificity of PCR amplification, called the annealing control primer (ACP), comprises a tripartite structure with a polydeoxyinosine [poly(dI)] linker between the 3' end target core sequence and the 5' end nontarget universal sequence. We show that this ACP linker prevents annealing of the 5' end nontarget sequence to the template and facilitates primer hybridization at the 3' end to the target sequence at specific temperatures, resulting in a dramatic improvement of annealing specificity. The effect of this linker is demonstrated by the incorporation of ACP sequences as primers during the amplification of target nucleotide sequence and as hybridization probes in the genotyping of single nucleotide polymorphisms. This is the first report to show that a poly(dI) linker between two different sequences of ACP forms a bubble-like structure and disrupts or destabilizes DNA duplex formation at certain annealing temperatures.

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