Email updates

Keep up to date with the latest news and content from BMC Hematology and BioMed Central.

Open Access Technical advance

Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR

Runa M Grimholt1*, Petter Urdal1, Olav Klingenberg2 and Armin P Piehler3

Author Affiliations

1 Department of Medical Biochemistry, Oslo University Hospital, Ullevaal, 0424 Oslo, Norway

2 Department of Medical Biochemistry, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway

3 Fürst Medical Laboratory, 1051 Oslo, Norway

For all author emails, please log on.

BMC Hematology 2014, 14:4  doi:10.1186/2052-1839-14-4

Published: 24 January 2014

Abstract

Background

Alpha-thalassemia is the most common human genetic disease worldwide. Copy number variations in the form of deletions of α-globin genes lead to α-thalassemia while duplications of α-globin genes can cause a severe phenotype in β-thalassemia carriers due to accentuation of globin chain imbalance. It is important to have simple and reliable methods to identify unknown or rare deletions and duplications in cases in which thalassemia is suspected but cannot be confirmed by multiplex gap-PCR. Here we describe a copy number variation assay to detect deletions and duplications in the α-globin gene cluster (HBA-CNV).

Results

Quantitative real-time PCR was performed using four TaqMan® assays which specifically amplify target sequences representing both the α-globin genes, the –α3.7 deletion and the HS-40 region. The copy number for each target was determined by the 2-ΔΔCq method. To validate our method, we compared the HBA-CNV method with traditional gap-PCR in 108 samples from patients referred to our laboratory for hemoglobinopathy evaluation. To determine the robustness of the four assays, we analyzed samples with and without deletions diluted to obtain different DNA concentrations. The HBA-CNV method identified the correct copy numbers in all 108 samples. All four assays showed the correct copy number within a wide range of DNA concentrations (3.2-100 ng/μL), showing that it is a robust and reliable method. By using the method in routine diagnostics of hemoglobinopathies we have also identified several deletions and duplications that are not detected with conventional gap-PCR.

Conclusions

HBA-CNV is able to detect all known large deletions and duplications affecting the α-globin genes, providing a flexible and simple workflow with rapid and reliable results.

Keywords:
α-thalassemia; Copy number variation; Quantitative real-time PCR; α-globin gene cluster; HS-40; Unknown deletions