Clinical, genetic, and pharmacogenetic applications of the invader assay

被引:106
作者
Kwiatkowski, RW [1 ]
Lyamichev, V [1 ]
de Arruda, M [1 ]
Neri, B [1 ]
机构
[1] Third Wave Technol Inc, Madison, WI 53719 USA
来源
MOLECULAR DIAGNOSIS | 1999年 / 4卷 / 04期
关键词
single-nucleotide polymorphism; genotyping; gene expression; fluorescence resonance energy transfer; Cleavase enzymes; mutation detection;
D O I
10.1016/S1084-8592(99)80012-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Invader technology has been developed for the detection of nucleic acids. It is a signal amplification system able to accurately quantify DNA and RNA targets with high sensitivity. Exquisite specificity is achieved by combining hybridization with enzyme recognition, which provides the ability to discriminate mutant from wild-type at ratios greater than 1/1000 (mutant/wt). The technology is isothermal and flexible and incorporates a homogeneous fluorescence readout. It is therefore readily adaptable for use in clinical reference laboratories, as well as high-through-put applications using 96-, 384-, and 1,536-well microtiter plate formats. The molecular mechanism of the system and specific applications for use in clinical and research laboratories are described. These include direct analysis of unamplified human genomic DNA to detect mutations and single-nucleotide polymorphisms associated with factor V Leiden, factor II, cystic fibrosis, and apolipoprotein E, and gene expression assays that quantify messenger RNA levels in cells using direct lysates.
引用
收藏
页码:353 / 364
页数:12
相关论文
共 31 条
  • [1] A helical arch allowing single-stranded DNA to thread through T5 5'-exonuclease
    Ceska, TA
    Sayers, JR
    Stier, G
    Suck, D
    [J]. NATURE, 1996, 382 (6586) : 90 - 93
  • [2] de Arruda M, 1998, AM J PATHOL, V153, P1651
  • [3] The helix-hairpin-helix DNA-binding motif: A structural basis for non-sequence-specific recognition of DNA
    Doherty, AJ
    Serpell, LC
    Ponting, CP
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (13) : 2488 - 2497
  • [4] Direct genetic analysis by matrix-assisted laser desorption ionization mass spectrometry
    Griffin, TJ
    Hall, JG
    Prudent, JR
    Smith, LM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) : 6301 - 6306
  • [5] Hall J, 1998, HEPATOLOGY, V28, p583A
  • [6] HALL JG, 1998, WIPO PUBLICATION
  • [7] THE CHARACTERIZATION OF A MAMMALIAN DNA STRUCTURE-SPECIFIC ENDONUCLEASE
    HARRINGTON, JJ
    LIEBER, MR
    [J]. EMBO JOURNAL, 1994, 13 (05) : 1235 - 1246
  • [8] DETECTION OF SPECIFIC POLYMERASE CHAIN-REACTION PRODUCT BY UTILIZING THE 5'-]3' EXONUCLEASE ACTIVITY OF THERMUS-AQUATICUS DNA-POLYMERASE
    HOLLAND, PM
    ABRAMSON, RD
    WATSON, R
    GELFAND, DH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) : 7276 - 7280
  • [9] Structure of the DNA repair and replication endonuclease and exonuclease FEN-1: Coupling DNA and PCNA binding to FEN-1 activity
    Hosfield, DJ
    Mol, CD
    Shen, BH
    Tainer, JA
    [J]. CELL, 1998, 95 (01) : 135 - 146
  • [10] The crystal structure of flap endonuclease-1 from Methanococcus jannaschii
    Hwang, KY
    Baek, K
    Kim, HY
    Cho, Y
    [J]. NATURE STRUCTURAL BIOLOGY, 1998, 5 (08) : 707 - 713