Rapid genotyping of single nucleotide polymorphisms using novel minor groove binding DNA oligonucleotides (MGB probes)

被引:106
作者
de Kok, JB [1 ]
Wiegerinck, ETG [1 ]
Giesendorf, BAJ [1 ]
Swinkels, DW [1 ]
机构
[1] Univ Med Ctr, Dept Clin Chem, Nijmegen, Netherlands
关键词
mutation detection; SNP; automation; screening; hemochromatosis; hereditary; HH; HFE; minor groove binding probe; MGB;
D O I
10.1002/humu.10076
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Novel fluorescent oligonucleotides that contain a 3' minor groove binding group (MGB) hybridize to single,stranded targets with increased sequence-specificity compared to ordinary DNA probes. This reduces non-specific probe hybridization and results in low background fluorescence during the 5' nuclease PCR assay (TaqMan, Applied Biosystems, Foster City, CA). We developed a method for closed-tube genotyping using two allele-specific MGB probes labeled with different fluorophores in one reaction. After PCR, tubes were transported to a fluorescence plate-reader for analysis of fluorescence. Common spreadsheet software was used for automated genotype assignment. As an example, DNA samples from 172 hemochromatosis patients were selected and tested for molecular defects in the HFE gene, i.e., mutations in codon 63 and 28.2. Tight genotype clusters were observed for both codons and results with MGB probes were identical to conventional genotyping (PCR + restriction-fragment-length-polymorphism). We show that this fast and easy method can be used for large,scale (high-throughput) genetic studies but also for routine molecular diagnostics without post-PCR manipulation of amplicons or the need for real,time quantitative PCR machines.
引用
收藏
页码:554 / 559
页数:6
相关论文
共 16 条
  • [1] Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder
    Afonina, I
    Zivarts, M
    Kutyavin, I
    Lukhtanov, E
    Gamper, H
    Meyer, RB
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (13) : 2657 - 2660
  • [2] Integrated amplification and detection of the C677T point mutation in the methylenetetrahydrofolate reductase gene by fluorescence resonance energy transfer and probe melting curves
    Bernard, PS
    Lay, MJ
    Wittwer, CT
    [J]. ANALYTICAL BIOCHEMISTRY, 1998, 255 (01) : 101 - 107
  • [3] Carella M, 1997, AM J HUM GENET, V60, P828
  • [4] Screening for hemochromatosis - A public health perspective
    Cogswell, ME
    Burke, W
    McDonnell, SM
    Franks, AL
    [J]. AMERICAN JOURNAL OF PREVENTIVE MEDICINE, 1999, 16 (02) : 134 - 140
  • [5] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
    Feder, JN
    Gnirke, A
    Thomas, W
    Tsuchihashi, Z
    Ruddy, DA
    Basava, A
    Dormishian, F
    Domingo, R
    Ellis, MC
    Fullan, A
    Hinton, LM
    Jones, NL
    Kimmel, BE
    Kronmal, GS
    Lauer, P
    Lee, VK
    Loeb, DB
    Mapa, FA
    McClelland, E
    Meyer, NC
    Mintier, GA
    Moeller, N
    Moore, T
    Morikang, E
    Prass, CE
    Quintana, L
    Starnes, SM
    Schatzman, RC
    Brunke, KJ
    Drayna, DT
    Risch, NJ
    Bacon, BR
    Wolff, RK
    [J]. NATURE GENETICS, 1996, 13 (04) : 399 - 408
  • [6] Giesendorf BAJ, 1998, CLIN CHEM, V44, P482
  • [7] DISSOCIATION KINETICS OF 19 BASE PAIRED OLIGONUCLEOTIDE-DNA DUPLEXES CONTAINING DIFFERENT SINGLE MISMATCHED BASE-PAIRS
    IKUTA, S
    TAKAGI, K
    WALLACE, RB
    ITAKURA, K
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (02) : 797 - 811
  • [8] Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis
    Jeffrey, GP
    Chakrabarti, S
    Hegele, RA
    Adams, PC
    [J]. NATURE GENETICS, 1999, 22 (04) : 325 - 326
  • [9] 3′-minor groove binder-DNA probes increase sequence specificity at PCR extension temperatures
    Kutyavin, IV
    Afonina, IA
    Mills, A
    Gorn, VV
    Lukhtanov, EA
    Belousov, ES
    Singer, MJ
    Walburger, DK
    Lokhov, SG
    Gall, AA
    Dempcy, R
    Reed, MW
    Meyer, RB
    Hedgpeth, J
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (02) : 655 - 661
  • [10] Allelic discrimination using fluorogenic probes and the 5′ nuclease assay
    Livak, KJ
    [J]. GENETIC ANALYSIS-BIOMOLECULAR ENGINEERING, 1999, 14 (5-6): : 143 - 149