Literature DB >> 9058242

Amplification of Guthrie card DNA: effect of guanidine thiocyanate on binding of natural whole blood PCR inhibitors.

G S Makowski1, E L Davis, S M Hopfer.   

Abstract

Amplification of DNA from whole blood collected on Guthrie card filter paper presents considerable technical obstacles due to the presence of natural PCR inhibitors (protein, heavy metals, heme, and heme degradation products) and low copy number of genomic material. For this purpose we evaluated guanidine thiocyanate-impregnated filter paper (GT-903), a DNA collection device designed specifically to bind PCR inhibitors and preserve DNA in an aqueous extractable form. Compared to standard 903, which retains DNA and elutes inhibitors during aqueous extraction, we found GT-903 retained 90% of protein, hemoglobin, and iron. SDS-PAGE analysis indicated that the majority of the protein released from standard 903 corresponded to albumin (70-) and globin (15-kDa); negligible levels of these proteins were eluted from GT-903. To evaluate PCR efficiency, we amplified the 491 bp region encoding the cystic fibrosis delta F508 mutation. Using comparable template, we found GT-903 amplification more efficient than standard 903 following qualitative (TBE-PAGE) and quantitative (anti-dsDNA EIA) determination. We conclude that GT-903 provides a good DNA collection device and addresses the complications associated with natural PCR inhibitors.

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Year:  1997        PMID: 9058242      PMCID: PMC6760716          DOI: 10.1002/(sici)1098-2825(1997)11:2<87::aid-jcla4>3.0.co;2-h

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  25 in total

1.  Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.

Authors:  B S Kerem; J Zielenski; D Markiewicz; D Bozon; E Gazit; J Yahav; D Kennedy; J R Riordan; F S Collins; J M Rommens
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

2.  Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening program.

Authors:  M Descartes; Y Huang; Y H Zhang; L L McCabe; R Gibbs; B L Therrell; E R McCabe
Journal:  Pediatr Res       Date:  1992-03       Impact factor: 3.756

3.  Methods for measuring plasma hemoglobin in micromolar concentration compared.

Authors:  V F Fairbanks; S C Ziesmer; P C O'Brien
Journal:  Clin Chem       Date:  1992-01       Impact factor: 8.327

4.  Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material.

Authors:  P S Walsh; D A Metzger; R Higuchi
Journal:  Biotechniques       Date:  1991-04       Impact factor: 1.993

5.  Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening.

Authors:  D C Jinks; M Minter; D A Tarver; M Vanderford; J F Hejtmancik; E R McCabe
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

6.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

7.  Enhanced direct amplification of Guthrie card DNA following selective elution of PCR inhibitors.

Authors:  G S Makowski; E L Davis; J Aslanzadeh; S M Hopfer
Journal:  Nucleic Acids Res       Date:  1995-09-25       Impact factor: 16.971

8.  In situ PCR amplification of Guthrie card DNA to detect cystic fibrosis mutations.

Authors:  G S Makowski; J Aslanzadeh; S M Hopfer
Journal:  Clin Chem       Date:  1995-03       Impact factor: 8.327

9.  DNA enzyme immunoassay: general method for detecting products of polymerase chain reaction.

Authors:  G Mantero; A Zonaro; A Albertini; P Bertolo; D Primi
Journal:  Clin Chem       Date:  1991-03       Impact factor: 8.327

10.  Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosis.

Authors:  C Verlingue; B Mercier; I Lecoq; M P Audrézet; D Laroche; G Travert; C Férec
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

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