Literature DB >> 11066011

Evaluation of chimerism in DNA samples by PCR amplification of D1S80 with detection by capillary electrophoresis.

C M Jone1, N Akel, A A Killeen.   

Abstract

BACKGROUND: Analysis of the relative amounts of donor and recipient DNA in bone marrow after bone marrow transplantation is frequently used to determine the status of the transplant. We studied the performance of an assay to quantify chimerism based on amplification of the D1S80 variable number tandem repeat marker by PCR with detection of PCR products by capillary electrophoresis (CE). METHODS AND
RESULTS: Samples from potential bone marrow donors and recipients were analyzed separately and in mixtures to simulate various degrees of chimerism from 10% to 90% and subjected to PCR/CE analysis. There was excellent agreement between the measured and known relative proportions of DNA components in chimeric samples. The lower limit of sensitivity for detection of chimerism was 1%; between-runs coefficients of variation were <5%.
CONCLUSIONS: Amplification of the D1S80 minisatellite by PCR with CE detection is a reliable method for determination of the relative contribution of different DNAs in mixed samples. This method is fast, quantitative, and extremely reproducible.

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Year:  2000        PMID: 11066011     DOI: 10.1007/bf03262028

Source DB:  PubMed          Journal:  Mol Diagn        ISSN: 1084-8592


  12 in total

1.  Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

Authors:  B Budowle; R Chakraborty; A M Giusti; A J Eisenberg; R C Allen
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

2.  Genetic typing by capillary electrophoresis with the allelic ladder as an absolute standard.

Authors:  N Zhang; E S Yeung
Journal:  Anal Chem       Date:  1996-09-01       Impact factor: 6.986

3.  DNA typing of a polymerase chain reaction amplified D1S80/amelogenin multiplex using capillary electrophoresis and a mixed entangled polymer matrix.

Authors:  A R Isenberg; B R McCord; B W Koons; B Budowle; R O Allen
Journal:  Electrophoresis       Date:  1996-09       Impact factor: 3.535

4.  Spanish population data on seven loci: D1S80, D17S5, HUMTH01, HUMVWA, ACTBP2, D21S11 and HLA-DQA1.

Authors:  M Lorente; J A Lorente; M R Wilson; B Budowle; E Villanueva
Journal:  Forensic Sci Int       Date:  1997-05-05       Impact factor: 2.395

5.  PCR-amplification and detection of the human D1S80 VNTR locus. Amplification conditions, population genetics and application in forensic analysis.

Authors:  A D Kloosterman; B Budowle; P Daselaar
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

6.  The impact of the PCR plateau phase on quantitative PCR.

Authors:  C Morrison; F Gannon
Journal:  Biochim Biophys Acta       Date:  1994-10-18

7.  D1S80 population data in African Americans, Caucasians, southeastern Hispanics, southwestern Hispanics, and Orientals.

Authors:  B Budowle; F S Baechtel; J B Smerick; K W Presley; A M Giusti; G Parsons; M C Alevy; R Chakraborty
Journal:  J Forensic Sci       Date:  1995-01       Impact factor: 1.832

8.  Chromosomal aneuploidy in leukemic blast crisis: a potential source of error in interpretation of bone marrow engraftment analysis by VNTR amplification.

Authors:  M Zhou; S Sheldon; N Akel; A A Killeen
Journal:  Mol Diagn       Date:  1999-06

9.  Capillary zone electrophoresis of polymerase chain reaction-amplified DNA fragments in polymer networks: the case of GATT microsatellites in cystic fibrosis.

Authors:  C Gelfi; A Orsi; P G Righetti; V Brancolini; L Cremonesi; M Ferrari
Journal:  Electrophoresis       Date:  1994-05       Impact factor: 3.535

10.  Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: the case of Kennedy's disease.

Authors:  M Nesi; P G Righetti; M C Patrosso; A Ferlini; M Chiari
Journal:  Electrophoresis       Date:  1994-05       Impact factor: 3.535

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