1 / 19

Proof of Principle for the Non-Invasive Prenatal Diagnosis of Fetal Trisomy 21

NE Thames Regional Genetics Service. Proof of Principle for the Non-Invasive Prenatal Diagnosis of Fetal Trisomy 21. Sarah Fielding 12-04-2010. Non-Invasive Aneuploidy Detection. Cell free fetal DNA and RNA detectable in maternal plasma Several diagnostic applications:

Download Presentation

Proof of Principle for the Non-Invasive Prenatal Diagnosis of Fetal Trisomy 21

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. NE Thames Regional Genetics Service Proof of Principle for the Non-Invasive Prenatal Diagnosis of Fetal Trisomy 21 Sarah Fielding 12-04-2010

  2. Non-Invasive Aneuploidy Detection • Cell free fetal DNA and RNA detectable in maternal plasma • Several diagnostic applications: • RhD typing in rhesus-negative mothers • Fetal sex determination • Inheritance of paternal mutations • Potential for detection of aneuploidies • <10% total cell-free DNA is fetal DNA • Sufficient for detection but… • INSUFFICIENT for quantitative analysis • Proposed solution – • Target sub-fraction of plasma nucleic acids that are completely fetal specific • Target fetal RNA of placental origin • Use fetal specific RNA markers to determine chromosome copy number QUALITATIVEDETECTION OF FETAL SPECIFIC SEQUENCE QUANTITATIVEASSESSMENT

  3. PLAC4 • 21q22.3 • Expressed exclusively by placenta Clearance of PLAC4 mRNA within 24hrs after delivery – specificity to pregnancy PLAC4 mRNA can be detected in all three trimesters of pregnancy but NOT in plasma of non-pregnant individuals Lo et al., 2007. Nature Medicine 13(2): 218-223

  4. Dosage of chromosome 21(RNA-SNP allelic ratio method) • Quantitative analysis of SNPs in PLAC4 mRNA Euploid pregnancy Trisomy 21 pregnancy T T T C C T:C 2: 1 T:C 1: 1 Allele Ratio

  5. RNA-SNP allelic ratio method • Lo et al (2007) – determined allelic ratio of PLAC4 SNP rs8130833 • Correctly identified 90% trisomy 21 cases in +ve controls • Excluded trisomy 21 in 96% normal controls • RNA-SNP allelic ratio method chosen for evaluation Lo et al., 2007. Nature Medicine 13(2): 218-223

  6. Testing Procedure • Stored in Trizol • RNeasy Kit (Qiagen) 1.6mL plasma 60 μ L of cfRNA (~15ng/ μL) • 8+1  9+3 weeks gestation • ABI Allelic Discrimination Assays

  7. PLAC4 mRNA Quantification • Real-time quantitative PCR • ABI7300 real-time PCR machine • Two steps (single reaction): • 1-step reverse transcription PCR • TaqMan real-time PCR • TaqMan MGB Probe • Detects PLAC4 PCR product • Reverse transcription -ve control • Standard curve used to determine quantity of PLAC4 mRNA • 7 standards with known quantity of PLAC4 amplicon

  8. PLAC4 mRNA Quantification - Results 5 replicates of cfRNA sample Plasma cfRNA Sample Quantity of PLAC4 mRNA ~ 21 copies/μL RT -ve • 8+5 week gestation pregnancy • In line with average 1st trimester PLAC4 mRNA conc. reported in literature

  9. PLAC4 SNP Genotyping • ABI SNP genotyping assays for 2 PLAC4 SNPs: • rs8130833(T 0.67/C 0.33) • rs7844 (G 0.63/C 0.37) • Each Assay: • 2 primers • 2 allele-specific TaqMan probes • Optimised to work directly with cfRNA • Two steps (single reaction) • 1-step reverse transcription PCR • Allelic Discrimination PCR • 60cycles • Whole reaction ~ 3.5 hours • Requires total 30μL cfRNA

  10. Results8+4 week gestation pregnancy – rs8130833 Fetal Genotype: T/T

  11. Results8+4 week gestation pregnancy – rs7844 Fetal Genotype: C/C

  12. Allele Dosage – VIC/FAM ratio • Need to determine allelic ratio of SNPs in het fetuses VIC FAM • Heterozygous Genotype Controls • rs8130833 (Mean VIC/FAM = 0.387; Std Dev = 0.012) • rs7844 (Mean VIC/FAM = 0.327; Std Dev = 0.009) • Hypothesis: • Het T21 sample with 2:1 or 1:2 allele ratio – • VIC/FAM ratio would deviate from het controls • Potential to discriminate between euploid and trisomy 21 cases consistent between samples with same genotype

  13. T21 simulation experiments VIC/FAM ratio: Mean for T/C Controls: 0.376 Mean for synthetic TTC: 0.722 (p=2.8x10-4) Mean for synthetic CCT: 0.210 (p=1.48x10-9)

  14. T21 sample • Maternal plasma aliquots from genuine T21 pregnancy • Parental samples genotyped • No result for rs7844 • Instrument error • Result for rs8130833 consistent with T21 & TTC fetal genotype

  15. T21 sample – rs8130833

  16. T21 sample – rs8130833

  17. T21 sample • Maternal plasma aliquots from genuine T21 pregnancy • Parental samples genotyped • Result for rs8130833 consistent with T21 & TTC fetal genotype • VIC/FAM ratio • Heterozygous T/C controls – 0.408 • T21 cfRNA sample – 0.866 • At rs8130833 – proof of principle demonstrated T-Test: p = 1.85 x 10-4

  18. Summary • Presence of fetal PLAC4 mRNA in maternal plasma successfully demonstrated and quantified • Method developed to determine allelic ratio of 2 PLAC4 SNPs using ABI allelic discrimination assays • Fetal PLAC4 mRNA from 8+4 week gestation pregnancy successfully genotyped at both loci • Analysis of cfRNA extracted from genuine T21 pregnancy supports results from T21 simulation experiments • Presented method can distinguish a T21 result from euploid result at ch21 PLAC4 SNP rs8130833

  19. Acknowledgements Gail Norbury Lucy Jenkins Lighta Godinho Bhaneeta Mistry & all staff Lyn Chitty Darryl Wang Guy’s Hospital North East Thames Regional Genetics Laboratory Institute of Child Health

More Related