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Arch Iran Med. 2011;14(3): 188-191.
PMID: 21529108
Scopus ID: 79961187675
  Abstract View: 3455
  PDF Download: 1710

Original Article

Gene Dosage Analysis of Proximal Spinal Muscular Atrophy Carriers using Real-Time PCR

Mohammad R. Abbaszadegan*, Fatemeh Keify*, Farah Ashrafzadeh, Moein Farshchian, Farhad Khadivi-Zand, Faezeh Mojahedi, Mohammad Naser Teymoorzadeh, Reza Ebrahimzadeh, Mitra Ahadian
*Corresponding Authors: Email: ; Email:

Abstract

BACKGROUND: Autosomal recessive spinal muscular atrophy is a disease resulting from homozygous absence of SMN1 gene in approximately 94% of SMA patients. To identify patients who retained a single SMN1 copy, SMN1 dosage analysis was performed by quantitative Real-time PCR using SYBR green dye. SMN1 dosage analysis results were utilized to identify carriers before offering prenatal diagnosis.

METHOD: Carrier testing was performed for 150 individuals. Copy number of the SMN1 gene was determined by the comparative threshold cycle (Ct) method and human serum albumin gene was used as a reference.

RESULT: Analysis of 150 DNA samples with quantitative PCR determined the number of SMN1 gene copies. Of these, 50 (33.33%) cases had one SMN1 gene copy, 87 (58%) had two copies and 13 (8.66%) did not have any copies of SMN1. The homozygous SMN1 deletion ratio was 0.00 and deletion of one copy of SMN1 gene ratio ranged from 0.3 to 0.58.

CONCLUSION: This report demonstrates modification of risk estimation for the diagnosis and detection of SMA carriers by accurate determination of SMN1 copy number. SMN1 copy number analysis is an important parameter for identification of couples at risk of having children affected with SMA. It also reduces unwarranted prenatal diagnosis for SMA. Furthermore, the dosage analysis might be useful for the counseling of clinically suspected SMA patients with negative diagnostic SMA tests

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