Establishment of pyrosequencing method for detection of Apolipoprotein E gene polymorphisms
10.16571/j.cnki.1008-8199.2019.05.008
- VernacularTitle: 焦磷酸测序检测载脂蛋白E基因多态性方法的建立
- Author:
Ya-nan CHU
1
;
Li-ying FENG
1
;
Yan-zi WU
1
;
Jie-yu ZHANG
1
Author Information
1. Department of Pharmacology,General Hospital of Easten Theater Command, PLA, Nanjing 210002, Jiangsu, China
- Publication Type:Journal Article
- Keywords:
pyrosequencing;
Apolipoprotein E;
rs7412;
rs429358
- From:
Journal of Medical Postgraduates
2019;32(5):490-494
- CountryChina
- Language:Chinese
-
Abstract:
Objective Apolipoprotein E (APOE) is mainly involved in lipid metabolism and cholesterol transport, which is important for health. To establish a pyrosequencing based method for detection of 112T>C and 158C>T single nucleotide polymorphisms (SNPs) in Apolipoprotein E gene. Methods Three amplification systems including Taq enzyme buffer from TaKaRa company (T buffer), La Taq enzyme buffer specified for G-C rich regions (L buffer) and Trans Taq enzyme buffer from TransGen company (TT buffer) were chosen to optimize PCR system and temperature by annealing at 60 °C and gradient annealing from 62 to 68 °C respectively. The specificity of this method was evaluated by comparing its results with those of Sanger sequencing. The sensitivity of this method was evaluated by gradient diluting human genomic DNA as detection template. Results According to the concentration and specificity of the products, the optimum condition was L buffer with 60℃ annealing programs. Pyrosequencing results of 20 samples were completely consistent with those of Sanger sequencing. The sensitivity of this method could be as low as 0.16 ng genomic DNA. Conclusion A method based on pyrosequencing detecting 112 and 158 polymorphisms in APOE gene was established, which can be applied in clinical personalized medicine.
