Unknown

Dataset Information

0

Quantification of PCR bias caused by a single nucleotide polymorphism in SMN gene dosage analysis.


ABSTRACT: Approximately 94% of patients with spinal muscular atrophy lack both copies of SMN1 exon 7, and most carriers have only one copy of SMN1 exon 7. We described previously the effect of SMN1/SMN2 heteroduplex formation on SMN gene dosage analysis, which is a multiplex quantitative PCR assay to determine the copy numbers of SMN1 and SMN2 using DraI digestion to differentiate SMN2 from SMN1. We describe herein the quantification of PCR bias between SMN1 exon 7 and SMN2 exon 7, which differ by only one nucleotide that is not present in either primer binding site. Using samples from 272 individuals with various SMN genotypes, we found that the amplification efficiency of SMN2 was consistent only approximately 80% that of SMN1. Thus, even a single nucleotide polymorphism, not in primer binding sites, can cause reproducible PCR bias. The precision and accuracy of our SMN gene dosage analysis are high because our assay design and controls take advantage of the consistency of the PCR bias. As additional clinically significant single nucleotide polymorphisms (SNPs) are discovered, assessment of PCR bias, and judicious selection of standards and controls, will be increasingly important for quantitative PCR assays.

SUBMITTER: Ogino S 

PROVIDER: S-EPMC3278980 | biostudies-literature | 2002 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Quantification of PCR bias caused by a single nucleotide polymorphism in SMN gene dosage analysis.

Ogino Shuji S   Wilson Robert B RB  

The Journal of molecular diagnostics : JMD 20021101 4


Approximately 94% of patients with spinal muscular atrophy lack both copies of SMN1 exon 7, and most carriers have only one copy of SMN1 exon 7. We described previously the effect of SMN1/SMN2 heteroduplex formation on SMN gene dosage analysis, which is a multiplex quantitative PCR assay to determine the copy numbers of SMN1 and SMN2 using DraI digestion to differentiate SMN2 from SMN1. We describe herein the quantification of PCR bias between SMN1 exon 7 and SMN2 exon 7, which differ by only on  ...[more]

Similar Datasets

| S-EPMC3237602 | biostudies-literature
| S-EPMC10778797 | biostudies-literature
| S-EPMC1472375 | biostudies-literature
| S-EPMC8687305 | biostudies-literature
| S-EPMC10624686 | biostudies-literature
| S-EPMC8048961 | biostudies-literature
| S-EPMC2034455 | biostudies-literature
| 2135070 | ecrin-mdr-crc
| S-EPMC311429 | biostudies-literature
| S-EPMC2607568 | biostudies-literature