Literature DB >> 2230693

Amplification of a variable number of tandem repeats (VNTR) locus (pMCT118) by the polymerase chain reaction (PCR) and its application to forensic science.

K Kasai1, Y Nakamura, R White.   

Abstract

A genetic locus (D1S58, defined by DNA probe pMCT118) that contains a variable number of tandem repeats (VNTR) has been successfully amplified from a very small amount of genomic deoxyribonucleic acid (DNA) by the polymerase chain reaction (PCR). The DNA sequence of the locus was determined and was found to consist of a 16-base consensus sequence and flanking sequences. Oligonucleotide primers complementary to the flanking sequences were synthesized to serve as primers for amplification of MCT118 by the PCR method. Human genomic DNA isolated from blood (2 ng from each sample) was successfully amplified at the MCT118 locus, and polymorphic bands were detectable by ethidium bromide staining after electrophoresis on polyacrylamide gels. Determination of genotypes at this VNTR locus can now be routinely achieved within 24 h, without the need for Southern blots or radioactive materials. Furthermore, the small size (387 to 723 base pairs) of the DNA fragments produced in the PCR amplification permits good resolution of individual alleles that differ by only one repeat unit. The precise specification of the number of tandem repeats present in each allelic fragment is reproducible from one analysis to another.

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Year:  1990        PMID: 2230693

Source DB:  PubMed          Journal:  J Forensic Sci        ISSN: 0022-1198            Impact factor:   1.832


  57 in total

1.  DNA flow cytometric quantification and DNA polymorphism analysis in the case of a complete mole with a coexisting fetus.

Authors:  M Hirose; T Kimura; N Mitsuno; K Wakuda; K Takakura; J Fujita; Y Noda
Journal:  J Assist Reprod Genet       Date:  1999-05       Impact factor: 3.412

2.  Population genetics and forensic efficiency data of 4 AMPFLP's.

Authors:  S Rand; C Puers; K Skowasch; P Wiegand; B Budowle; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

3.  Human population genetic studies using hypervariable loci. I. Analysis of Assamese, Australian, Cambodian, Caucasian, Chinese and Melanesian populations.

Authors:  I Balazs; J Neuweiler; P Gunn; J Kidd; K K Kidd; J Kuhl; L Mingjun
Journal:  Genetics       Date:  1992-05       Impact factor: 4.562

4.  pMCT 118 (D1S80): a new allelic ladder and an improved electrophoretic separation lead to the demonstration of 28 alleles.

Authors:  K Skowasch; P Wiegand; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

5.  PCR amplification of alleles at the DIS80 locus: comparison of a Finnish and a North American Caucasian population sample, and forensic casework evaluation.

Authors:  A Sajantila; B Budowle; M Ström; V Johnsson; M Lukka; L Peltonen; C Ehnholm
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

6.  Genetic analysis using fingernail DNA.

Authors:  T Kaneshige; K Takagi; S Nakamura; T Hirasawa; M Sada; K Uchida
Journal:  Nucleic Acids Res       Date:  1992-10-25       Impact factor: 16.971

7.  Optimized amplification of the polymorphic system COL2A1.

Authors:  K Skowasch; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

8.  A new sequenced allelic ladder marker for D1S80 typing.

Authors:  Koji Fujii; Kazumasa Sekiguchi; Kenshi Shimizu; Kentaro Kasai
Journal:  J Hum Genet       Date:  2004-02-26       Impact factor: 3.172

9.  Problems associated with the DNA analysis of stains.

Authors:  S Rand; P Wiegand; B Brinkmann
Journal:  Int J Legal Med       Date:  1991       Impact factor: 2.686

10.  Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.

Authors:  J Reiss; D N Cooper; J Bal; R Slomski; G R Cutting; M Krawczak
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

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