Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma--case report

Y Li, W Holzgreve, G C M L Page-Christiaens, J J P Gille, S Hahn

Research output: Contribution to journalArticleAcademicpeer-review

75 Citations (Scopus)

Abstract

INTRODUCTION: The efficacious analysis of fetal loci involving point mutations from circulatory fetal DNA in maternal plasma is hindered by the preponderance of maternal DNA. It has recently been shown that the size difference between fetal and maternal DNA species can be used for the selective enrichment of circulatory fetal DNA in maternal plasma. We have now tested this approach for the detection of a fetal point mutation in the fibroblast growth factor receptor 3 (FGFR3) gene that causes achondroplasia.

METHODS: Circulatory DNA was extracted from maternal plasma and size-fractionated by agarose gel electrophoresis. The fraction with a size less than 300 bp was examined by a touchdown PCR assay specific for the FGFR3 gene, and the mutation was identified by SfcI restriction analysis.

RESULT: Our analysis indicated that although the fetal mutation was discernible in the analysis of total plasma DNA, the result using size-fractionated DNA was much more evident.

CONCLUSION: The enrichment of circulatory fetal DNA in maternal plasma by size-fractionation facilitates the detection of subtle feto-maternal genetic differences, such as those involving point mutations. This approach can easily be extended for the non-invasive prenatal determination of other fetal loci.

Original languageEnglish
Pages (from-to)896-8
Number of pages3
JournalPrenatal diagnosis
Volume24
Issue number11
DOIs
Publication statusPublished - Nov 2004

Keywords

  • Achondroplasia/blood
  • Adult
  • Amniocentesis
  • DNA/analysis
  • Diagnosis, Differential
  • Female
  • Fetus/cytology
  • Humans
  • Mutation
  • Polymerase Chain Reaction
  • Pregnancy
  • Pregnancy Trimester, Third
  • Prenatal Diagnosis
  • Protein-Tyrosine Kinases/analysis
  • Receptor, Fibroblast Growth Factor, Type 3
  • Receptors, Fibroblast Growth Factor/analysis

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