HIGH-SENSITIVE FLUORESCENT DNA SEQUENCING AND ITS APPLICATION FOR DETECTION AND MASS-SCREENING OF POINT MUTATIONS

被引:43
作者
HATTORI, M [1 ]
YOSHIOKA, K [1 ]
SAKAKI, Y [1 ]
机构
[1] KYUSHU UNIV,GENET INFORMAT RES LAB,FUKUOKA 812,JAPAN
关键词
D O I
10.1002/elps.11501301114
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a rapid and sensitive DNA sequencing method for an automated fluorescent DNA sequencer (AFDS) and its application for detection of point mutations. The method is based on an improved cycle sequencing procedure in which only 10-50 fmol of template DNA is required. Furthermore, it is able to use crude DNA preparation as a template as well as the purified one. Thus, the improved method provided a simplified procedure for sequencing of various types of DNA, including cosmid DNA, in which purification steps were unnecessary. We also developed a novel system for detection of point mutations using AFDS. A set of four lanes is used for the parallel analysis of single-base profiles of four different samples, instead of for the four-base profile of a sample. The AFDS exhibits the base profiles of the samples with four different colors in the analyzed data, which enables us to identify a mutation as an additional peak with a color specific for the lane. The feasibility of our system was tested by analyzing polymerase chain reaction (PCR)-amplified genomic DNAs from four individuals including a carrier of a mutation of C to T. The mutation was clearly identified as an additional "T" peak of a color specific for the carrier. The mutation was also detectable even if 16 individuals including the carrier were simultaneously analyzed on a set of four lanes (four individual samples for each lane). Thus, the novel system is useful for simultaneous detection of mutations in a large number of individual samples.
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页码:560 / 565
页数:6
相关论文
共 22 条
  • [1] A NONRADIOACTIVE AUTOMATED-METHOD FOR DNA-SEQUENCE DETERMINATION
    ANSORGE, W
    SPROAT, BS
    STEGEMANN, J
    SCHWAGER, C
    [J]. JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1986, 13 (06): : 315 - 323
  • [2] Bevan I S, 1992, PCR Methods Appl, V1, P222
  • [3] CAROTHERS AM, 1989, BIOTECHNIQUES, V7, P494
  • [4] SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE
    GOATE, A
    CHARTIERHARLIN, MC
    MULLAN, M
    BROWN, J
    CRAWFORD, F
    FIDANI, L
    GIUFFRA, L
    HAYNES, A
    IRVING, N
    JAMES, L
    MANT, R
    NEWTON, P
    ROOKE, K
    ROQUES, P
    TALBOT, C
    PERICAKVANCE, M
    ROSES, A
    WILLIAMSON, R
    ROSSOR, M
    OWEN, M
    HARDY, J
    [J]. NATURE, 1991, 349 (6311) : 704 - 706
  • [5] GENERATION OF SINGLE-STRANDED-DNA BY THE POLYMERASE CHAIN-REACTION AND ITS APPLICATION TO DIRECT SEQUENCING OF THE HLA-DQA LOCUS
    GYLLENSTEN, UB
    ERLICH, HA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (20) : 7652 - 7656
  • [6] DIDEOXY SEQUENCING METHOD USING DENATURED PLASMID TEMPLATES
    HATTORI, M
    SAKAKI, Y
    [J]. ANALYTICAL BIOCHEMISTRY, 1986, 152 (02) : 232 - 238
  • [7] LARGE-SCALE AND AUTOMATED DNA-SEQUENCE DETERMINATION
    HUNKAPILLER, T
    KAISER, RJ
    KOOP, BF
    HOOD, L
    [J]. SCIENCE, 1991, 254 (5028) : 59 - 67
  • [8] A SIMPLE AND RAPID PREPARATION OF M13 SEQUENCING TEMPLATES FOR MANUAL AND AUTOMATED DIDEOXY SEQUENCING
    KRISTENSEN, T
    VOSS, H
    ANSORGE, W
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (14) : 5507 - 5516
  • [9] LITTLE PFR, 1987, DNA CLONING PRACTICA, V3, P19
  • [10] Maniatis T., 1982, MOL CLONING