Specific triplex binding capacity of mixed base sequence duplex nucleic acids used for single-nucleotide polymorphism detection

被引:7
|
作者
Daksis, JI [1 ]
Erikson, GH [1 ]
机构
[1] Ingeneus Res, Unit 5, Mississauga, ON L4Z 1V4, Canada
来源
GENETIC TESTING | 2005年 / 9卷 / 02期
关键词
D O I
10.1089/gte.2005.9.111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Specific base recognition and binding between native double-stranded DNA ( dsDNA) and complementary single-stranded DNA (ssDNA) of mixed base sequence is presented. Third-strand binding, facilitated and stabilized by a DNA intercalator, YOYO-1, occurs within 5 min at room temperature. This triplex binding capability has been used to develop a homogeneous assay that accurately detects 1-, 2-, or 3-bp mutations or deletions in the dsDNA target. Every type of 1- bp mismatch can be identified. The assay can reliably distinguish homozygous from heterozygous polymerase chain reaction (PCR) - amplified genomic dsDNA, thus providing a highly sensitive clinical diagnostic assay.
引用
收藏
页码:111 / 120
页数:10
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