Allele-specific polymerase chain reaction for the detection of Alzheimer’s disease-related single nucleotide polymorphisms
详细信息    查看全文
  • 作者:Mohd Nazif Darawi (1)
    Chin Ai-Vyrn (2)
    Kalavathy Ramasamy (3)
    Philip Poi Jun Hua (2)
    Tan Maw Pin (2)
    Shahrul Bahyah Kamaruzzaman (2)
    Abu Bakar Abdul Majeed (1) (4)
  • 关键词:Alzheimer’s disease ; Single nucleotide polymorphism ; Apolipoprotein E ; Bridging integrator ; Clusterin ; ATP ; binding cassette sub ; family A member 7 ; Complement receptor 1 ; Phosphatidylinositol binding clathrin assembly protein ; Allele ; specific polymerase chain reaction
  • 刊名:BMC Medical Genetics
  • 出版年:2013
  • 出版时间:December 2013
  • 年:2013
  • 卷:14
  • 期:1
  • 全文大小:495KB
  • 参考文献:1. Wimo A, Winblad B, J?nsson L: The worldwide societal costs of dementia: estimates for 2009. / Alzheimers Dement 2010, 6:98-03. CrossRef
    2. Bekris LM, Yu CE, Bird TD, Tsuang DW: Genetics of Alzheimer’s disease. / J Geriat Psychiatry Neurol 2010, 23:213-27. CrossRef
    3. Borenstein AR, Copenhaver CI, Mortimer JA: Early-life risk factors for Alzheimer’s disease. / Alzheimer Dis Assoc Disord 2006, 20:63-2. CrossRef
    4. Bertram L, Tanzi RE: Thirty years of Alzheimer’s disease genetics: the implications of systematic meta-analyses. / Nat Rev Neurosci 2008, 9:768-78. CrossRef
    5. Mayeux R, Saunders AM, Shea S, Mirra S, Evans D, Hyman BT, Crain B, Tang MX, Phelps CH: Utility of the apolipoprotein E genotype in the diagnosis of Alzheimer’s disease. / N Engl J Med 1998, 338:506-11. CrossRef
    6. Bertram L, McQueen MB, Mullin K, Blacker D, Tanzi RE: Systematic meta-analyses of Alzheimer’s disease genetic association studies: the AlzGene database. / Nat Genet 2007, 39:17-3. CrossRef
    7. Kwok PY, Chen X: Detection of single nucleotide polymorphisms. / Curr Issues Mol Biol 2003, 5:43-0.
    8. Newton CR, Graham A, Hepstinstall LE, Powell SJ, Summers C, Kalsheker N, Smith JC, Markham AF: Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). / Nucleic Acids Res 1989, 17:2503-516. CrossRef
    9. Myakishev MV, Khiripin Y, Hu S, Hamer HD: High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers. / Genome Res 2001, 11:163-69. CrossRef
    10. Germer S, Higuchi R: Single-tube genotyping without oligonucleotide probes. / Genome Res 1999, 9:72-8.
    11. Teh LK, Lee WL, Amir J, Salleh MZ, Ismail R: Single step PCR for detection of allelic variation of MDR1 gene (P-glycoprotein) among three ethnic groups in Malaysia. / J J Clin Pharm Ther 2007, 32:313-19. CrossRef
    12. Chen Q, Lu P, Jones AV, Cross NC, Silver RT, Wang L: Amplification refractory mutation system, a highly sensitive and simple polymerase chain reaction assay, for the detection of JAK2 V617F mutation in chronic myeloproliferative disorders. / J Mol Diagn 2007, 9:272-76. CrossRef
    13. Mirasena S, Shimbhu D, Sanguansermsri M, Sanguansermsri T: Detection of beta-thalassemia mutations using a multiplex amplification refractory mutation system assay. / Hemoglobin 2008, 32:403-09. CrossRef
    14. Sapkota BR, Ranjit C, Neupane KD, Macdonald M: Development and evaluation of a novel multipleprimer PCR amplification refractory mutation system for the rapid detection of mutations conferring rifampicin resistance in codon 425 of the rpoB gene of mycobacterium leprae. / J Med Microbiol 2008, 57:179-84. CrossRef
    15. Wenham PR, Newton CR, Price WH: Analysis of apolipoprotein E genotypes by the amplification refractory mutation system. / Clin Chem 1991, 37:241-44.
    16. Donohoe GG, Salomaki A, Lehtimaki T, Pulkki K, Kairisto V: Rapid identification of apolipoprotein E genotypes by multiplex amplification refractory mutation system PCR and capillary gel electrophoresis. / Clin Chem 1999, 45:143-46.
    17. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ: Basic local alignment search tool. / J Mol Biol 1990, 215:403-10.
    18. Mammedov TG, Pienaar E, Whitney SE, TerMaat JR, Carvill G, Goliath R, Subramaniam A, Viljoen HJ: A fundamental study of the PCR amplification of GC-rich DNA templates. / Comput Biol Chem 2008, 32:452-57. CrossRef
    19. Hixson JE, Vernier DT: Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with Hhal. / J Lipid Res 1990, 31:545-48.
    20. Koch W, Ehrenhaft A, Griesser K, Pfeufer A, Müller J, Sch?mig A, Kastrati A: TaqMan systems for genotyping of disease-related polymorphisms present in the gene encoding apolipoprotein E. / Clin Chem Lab Med 2002, 40:1123-131. CrossRef
    21. Aydin A, Toliat MR, B?hring S, Becker C, Nürnberg P: New universal primers facilitate pyrosequencing. / Electrophoresis 2006, 27:394-97. CrossRef
    22. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2350/14/27/prepub
  • 作者单位:Mohd Nazif Darawi (1)
    Chin Ai-Vyrn (2)
    Kalavathy Ramasamy (3)
    Philip Poi Jun Hua (2)
    Tan Maw Pin (2)
    Shahrul Bahyah Kamaruzzaman (2)
    Abu Bakar Abdul Majeed (1) (4)

    1. Brain Science Research Laboratory, Faculty of Pharmacy, Universiti Teknologi MARA, Puncak Alam, Selangor, 42300, Malaysia
    2. Ageing and Age Associated Disorders Research Group, Department of Medicine, Faculty of Medicine, University Malaya, Kuala Lumpur, 50603, Malaysia
    3. Collaborative Drug Discovery Research Group, Faculty of Pharmacy, Universiti Teknologi MARA, Puncak Alam, Selangor, 42300, Malaysia
    4. Research Management Institute, Universiti Teknologi MARA, Shah Alam, Selangor, 40450, Malaysia
  • ISSN:1471-2350
文摘
Background The incidence of Alzheimer’s disease, particularly in developing countries, is expected to increase exponentially as the population ages. Continuing research in this area is essential in order to better understand this disease and develop strategies for treatment and prevention. Genome-wide association studies have identified several loci as genetic risk factors of AD aside from apolipoprotein E such as bridging integrator (BIN1), clusterin (CLU), ATP-binding cassette sub-family A member 7 (ABCA7), complement receptor 1 (CR1) and phosphatidylinositol binding clathrin assembly protein (PICALM). However genetic research in developing countries is often limited by lack of funding and expertise. This study therefore developed and validated a simple, cost effective polymerase chain reaction based technique to determine these single nucleotide polymorphisms. Methods An allele-specific PCR method was developed to detect single nucleotide polymorphisms of BIN1 rs744373, CLU rs11136000, ABCA7 rs3764650, CR1 rs3818361 and PICALM rs3851179 in human DNA samples. Allele-specific primers were designed by using appropriate software to permit the PCR amplification only if the nucleotide at the 3-end of the primer complemented the base at the wild-type or variant-type DNA sample. The primers were then searched for uniqueness using the Basic Local Alignment Search Tool search engine. Results The assay was tested on a hundred samples and accurately detected the homozygous wild-type, homozygous variant-type and heterozygous of each SNP. Validation was by direct DNA sequencing. Conclusion This method will enable researchers to carry out genetic polymorphism studies for genetic risk factors associated with late-onset Alzheimer’s disease (BIN1, CLU, ABCA7, CR1 and PICALM) without the use of expensive instrumentation and reagents.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700