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J Res Med Sci 2017,  22:100

Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients


1 Department of Laboratory Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
2 Medical Genetics Laboratory of Genome, Tehran, Iran
3 PHD Candidate of Genetics at National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
4 Department of Radiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
5 Medical Genetics Laboratory of Genome, Tehran; Department of Genetics and Molecular Biology, Isfahan University of Medical Sciences, Isfahan, Iran
6 Cardiovascular Research Center, Isfahan Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
7 Department of Biotechnology, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Date of Submission13-Jan-2017
Date of Decision05-Mar-2017
Date of Acceptance10-May-2017
Date of Web Publication16-Aug-2017

Correspondence Address:
Mansoor Salehi
Department of Genetic and Molecular Biology, Isfahan University of Medical Sciences, Isfahan
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jrms.JRMS_874_16

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  Abstract 

Background: Mutations in the acid alpha-glucosidase (GAA) gene usually lead to reduced GAA activity. In this study, we analyzed the mutations of GAA and GAA enzyme activity from one sibling suspected Pompe disease and their first-degree relatives. Materials and Methods: In this cross-sectional study, GAA enzyme activity assay was assessed using tandem mass spectrometry. Polymerase chain reaction and Sanger sequencing were performed for GAA analysis. Results: GAA enzyme activity was significantly decreased in patients compared to the normal range (P = 0.02). Two individuals showed ten alterations in the GAA sequence, in which one of them (c. 1650del G) has not been previously described in the literature. A single Guanine deletion (del-G) was detected at codon 551 in exon 12. Conclusion: According to the literature, the detected change is a novel mutation. We hypothesized that the discovered deletion in the GAA might lead to a reduced activity of the gene product.

Keywords: Acid alpha-glucosidase, novel mutation, polymerase chain reaction, Pompe disease


How to cite this article:
Ebrahimi M, Behnam M, Behranvand-jazi N, Yari L, Sheikh-kanlomilan S, Salehi M, Tahmasebi P, Amini M, Behjati M, Hosseini N. Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients. J Res Med Sci 2017;22:100

How to cite this URL:
Ebrahimi M, Behnam M, Behranvand-jazi N, Yari L, Sheikh-kanlomilan S, Salehi M, Tahmasebi P, Amini M, Behjati M, Hosseini N. Identification a novel mononucleotide deletion mutation in GAA in pompe disease patients. J Res Med Sci [serial online] 2017 [cited 2017 Sep 25];22:100. Available from: http://www.jmsjournal.net/text.asp?2017/22/1/100/213063


  Introduction Top


Pompe disease, a glycogen storage disease (GSD) Type II (OMIM 232300), is characterized by a deficiency of the normal function enzyme acid alpha-glucosidase (GAA) that results in intralysosomal accumulation of glycogen. Clinical heterogeneity is a pivotal characteristic of Pompe disease which reveals importance of investigations in different populations.[1],[2] This heterogeneity occurs due to many mutations in the GAA gene which cause incomplete or complete lack of GAA activity and also different clinical manifestations.[2],[3],[4] The GAA is located on chromosome 17q25.2–25.3 which contains twenty exons and is highly polymorphic with a large number of neutral variations.[5] To the best of our knowledge, 351 disease-causing mutations have been described in the GAA, however, the leaky c-32-13T>G (usually known as IVS1-13T>G) is the most frequent mutation among the Caucasian Pompe disease patients.[6],[7] Therefore, in this study, we aimed to analyze the GAA and GAA enzyme activity from one sibling suspected Pompe disease and their first-degree relatives.


  Materials and Methods Top


Study population

An Iranian couple with three children, a 26-year-old affected son, a 34-year-old affected daughter, and a 31-year-old healthy daughter were referred to our center, Isfahan, Iran. In this cross-sectional study, due to the very low prevalence of Pompe disease and also based on low sample size of previous studies, we investigated mutations of GAA gene in two patients with Pompe. Both patients are resident of Semnan Province. Research protocols and consent forms were approved by the Genome Research Center (Code: G-1263).

Enzyme activity and polymerase chain reaction

For confirmation of the diagnosis, an enzyme activity assay test to determine reduced or no activity of the GAA enzyme is required. GAA enzyme activity assay was assessed using tandem mass spectrometry.

Genomic DNA was extracted from total blood using DNA extraction Spin Kit (GE Healthcare UK Ltd., Buckinghamshire, UK) according to the manufacturer's instructions. Polymerase chain reaction and Sanger sequencing were performed for GAA analysis.

Statistical analysis

Data were collected and then SPSS for software (version 20.0; SPSS Chicago, IL, USA) was used for statistical analysis. The comparison of GAA enzyme activity between Pompe patients and the lower limit of normal range of GAA enzyme activity was performed using one-sample t-test.


  Results Top


Enzyme activity

Both patients had more than 17% reduction in the GAA activity (range: 0.13–0.19 nmol/spot*21 h) compared to the normal range (>0.9 nmol/spot*21 h) [Table 1]. The patients had elevated serum levels of creatine phosphokinase and liver enzymes (aspartate aminotransferase and alanine aminotransferase) ranging from 2 to 10-fold of the normal ranges.
Table 1: Measured acid alpha-glucosidase activity of the affected individual in comparison to the reference values, which shows significant differences

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Genotyping

Our study revealed ten alterations in the patients. According to Pompe Center, one of the alterations was novel, and nine of them were previously reported. These alterations in the GAA were eight single-nucleotide polymorphisms (SNP) and two mutations including one deletion mutation and one large deletion splice site mutation. The new alteration c.1650del G was found in two children of this family. Molecular analysis revealed two heterozygous mutations including a deletion of a single guanine in exon 12 at codon 551 and a large deletion in intron 1. Sequencing of GAA in other member of this family revealed that father, the healthy daughter and one affected of the children were heterozygous for the c. 32-13T>G mutation, while the mother was normal for this mutation. For this new deletion mutation, the both of father and healthy daughter were normal, but mother and affected children were heterozygous.


  Discussion Top


Our data confirmed the clinical manifestations of GSDII in the patients. In addition, the activity of GAA approved the molecular genetic results. The activity of GAA at PH 3.8 with and without specific inhibition was less than the normal ranges. Two patients had similar GAA activity and GAA alterations. Different clinical symptoms in these two patients may in part be clarified by the existence of other variants in GAA gene or other related genes. GAA mutations are located on different parts of the gene and include missense, nonsense, splicing, and both small and large deletions and insertions. Although most of the mutations related to GSDII are located on limited numbers of regions, some of them are common in especial ethnical populations.[8] The most common mutation is IVS1-13T>G, which seen in approximately 77% of patients with Pompe who are from different ethnic populations. The presence of this mutation result in improper splicing in 80%–90% of the GAA premessenger RNA splicing events.[9] Although this mutation was found in our cases, the father of this family was homozygous. In this regard, Musumeci et al.[10] reported six Pompe patients who were homozygous for c. 32-13T>G mutation. The new mutation c. 1650delG was heterozygous in two patients and their mother. The female patient showed higher severity in clinical symptoms compared to his brother. The low enzyme activity of GAA of patients was in line with the presence of the alteration in c. 32-13T>G and c.1650delG. However, further investigations in different populations will be required to establish these mutations in the GAA gene of Pompe patients.


  Conclusion Top


According to the literature, the detected change is a novel mutation. We hypothesized that the discovered deletion in the GAA might lead to a reduced activity of the gene product.

Acknowledgments

We would like to thank patients and their family for their ongoing commitments. In addition, we thank of Dr. Morteza Purfarzam and Dr. Shahriyar Nafisi.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
Hagemans ML, Winkel LP, Van Doorn PA, Hop WJ, Loonen MC, Reuser AJ, et al. Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients. Brain 2005;128(Pt 3):671-7.  Back to cited text no. 1
    
2.
Cabrera López JC, Marti Herrero M, Fernández Burriel M, Toledo L, de Andrés-Cofiño R, Orera MA. Familial Pitt-Rogers-Danks: Two new cases. Rev Neurol 2001;33:439-43.  Back to cited text no. 2
    
3.
Chan J, Desai AK, Kazi ZB, Corey K, Austin S, Hobson-Webb LD, et al. The emerging phenotype of late-onset Pompe disease: A systematic literature review. Mol Genet Metab 2017;120:163-72.  Back to cited text no. 3
    
4.
Hirschhorn R. Glycogen storage disease type II; acid α-glucosidase (acid maltase) deficiency. The metabolic and molecular bases of inherited disease. 2001.  Back to cited text no. 4
    
5.
Raben N, Plotz P, Byrne BJ. Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease). Curr Mol Med 2002;2:145-66.  Back to cited text no. 5
    
6.
Engel AG, Seybold ME, Lambert EH, Gomez MR. Acid maltase deficiency: Comparison of infantile, childhood, and adult types. Neurology 1970;20:382.  Back to cited text no. 6
    
7.
Huie ML, Chen AS, Tsujino S, Shanske S, DiMauro S, Engel AG, et al. Aberrant splicing in adult onset glycogen storage disease type II (GSDII): Molecular identification of an IVS1 (-13T-->G) mutation in a majority of patients and a novel IVS10 (+1GT-->CT) mutation. Hum Mol Genet 1994;3:2231-6.  Back to cited text no. 7
    
8.
Hermans MM, van Leenen D, Kroos MA, Beesley CE, Van Der Ploeg AT, Sakuraba H, et al. Twenty-two novel mutations in the lysosomal alpha-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II. Hum Mutat 2004;23:47-56.  Back to cited text no. 8
    
9.
Winkel LP, Hagemans ML, van Doorn PA, Loonen MC, Hop WJ, Reuser AJ, et al. The natural course of non-classic Pompe's disease; a review of 225 published cases. J Neurol 2005;252:875-84.  Back to cited text no. 9
    
10.
Musumeci O, Thieme A, Claeys KG, Wenninger S, Kley RA, Kuhn M, et al. Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrum. Neuromuscular disorders: NMD 2015;25:719-24.  Back to cited text no. 10
    



 
 
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