| Literature DB >> 18968561 |
Hiroyoshi Miyahara1, Kenichi Yamashita, Masayuki Kanai, Kazuhiko Uchida, Makoto Takagi, Hiroki Kondo, Shigeori Takenaka.
Abstract
Single nucleotide polymorphisms (SNPs) of cancer repression gene p53 were analyzed electrochemically with ferrocenyl naphthalene diimide (1) as a hybridization indicator. The SNPs studied were the transition to A from G in the codon for amino acid at positions 175, 248 or 273 and the transversion to C from G in the codon for the amino acid at position 72. Thus, 20-meric oligonucleotides carrying the SNP site were used both as a sample and a probe with the latter immobilized on an electrode. Even one base difference on the p53 gene resulted in a significant difference in the current response of 1 and the magnitude of the response correlated with the amount of the DNA hybrid on the electrode. Moreover, when PCR products of exon 4, on which the P72/R72 SNP resides, of the p53 gene were analyzed by this method, the heterozygote and homozygotes were discriminated with modest precision.Entities:
Year: 2002 PMID: 18968561 DOI: 10.1016/s0039-9140(01)00652-x
Source DB: PubMed Journal: Talanta ISSN: 0039-9140 Impact factor: 6.057