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Cell Journal، جلد ۱۸، شماره ۳، صفحات ۴۰۵-۴۱۵

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عنوان انگلیسی Mitochondrial Copy Number and D-Loop Variants in Pompe Patients
چکیده انگلیسی مقاله Objective: Pompe disease is a rare neuromuscular genetic disorder and is classified into two forms of early and late-onset. Over the past two decades, mitochondrial abnormalities have been recognized as an important contributor to an array of neuromuscular diseases. We therefore aimed to compare mitochondrial copy number and mitochondrial displacement-loop sequence variation in infantile and adult Pompe patients. Materials and methods: In this retrospective study, the mitochondrial D-loop sequence was analyzed by polymerase chain reaction (PCR) and direct sequencing to detect possible variation in 28 Pompe patients (17 infants and 11 adults). Results were compared with 100 healthy controls and sequences of all individuals were compared with the Cambridge reference sequence. Real-time PCR was used to quantify mitochondrial DNA copy number. Results: Among 59 variants identified, 37(62.71%) were present in the infant group, 14(23.333%) in the adult group and 8(13.333%) in both groups. Mitochondrial copy number in infant patients was lower than adults (P< 0.05). A significant frequency difference was seen between the two groups for 12 single nucleotide polymorphism (SNP). A novel insertion (317-318 ins CCC) was observed in patients and six SNPs were identified as neutral variants in controls. There was an inverse association between mitochondrial copy number and D-loop variant number (r=0.54). Conclusion: The 317-318 ins CCC was detected as a new mitochondrial variant in Pompe patients.
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نویسندگان مقاله فاطمه بحرینی | fatemeh bahreini


مسعود هوشمند | massoud houshmand


محمد حسین مدرسی | mohammad hossein modaresi


حسن تنکابنی | hassan tonekaboni


شهریار نفیسی | shahriar nafissi


ferdoss نظری | ferdoss nazari


سید محمد اکرمی | seyed mohammad akrami



نشانی اینترنتی http://celljournal.org/journal/article/abstract/4569
فایل مقاله اشکال در دسترسی به فایل - ./files/site1/rds_journals/16/article-16-367070.pdf
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زبان مقاله منتشر شده en
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