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少量细胞模板下多重置换扩增技术的保真度评估

Evaluation of the fidelity of multiple displacement amplification from small number of cells
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摘要 目的应用单核苷酸多态性(single nucleotide polymorphism,SNP)芯片,检测以少量细胞(1~10个)为模板的多重置换扩增(multiple displacement amplification,MDA)产物的保真度。方法结合10K2.0SNP芯片平台与MDA,以纤维母细胞系GM02732(47,XY,+18)作为模板,共分6组进行实验,其中A组与B组分别为阳性对照组(细胞gDNA)与阴性对照组(无模板MDA);C-F组为实验组,分别以1、2、5和10个细胞为模板进行MDA扩增,产物与芯片杂交,检测并比较各组产物的基因组覆盖率、等位基因杂合性缺失(loss of heterozygosity,LOH)率以及等位基因脱扣(allele dropout,ADO)率。结果阴性对照组的MDA产物与gDNA序列有3.2%的重叠。随着起始模板从单细胞提升至10细胞,MDA产物的基因组覆盖率从86.4%逐步上升至96.4%,平均LOH率和ADO率则逐渐下降,各组之间比较差异均有统计学意义(P〈0.05)。结论多重置换扩增技术是一种高效而可靠的全基因组扩增方法,随着模板细胞的增加,MDA产物的保真度可获得明显的改善。10K 2.0SNP芯片可快速准确地在全基因组水平对DNA扩增产物进行保真度分析,但应注意区分LOH中的ADO和等位基因优势扩增,以避免产生误差。 Objective To evaluate the fidelity of multiple displacement amplification (MDA) from small number of cells (1-10 cells) by 10K 2.0 SNP mapping array. Methods A fibroblast cell line (Tri-18; GM02732, 47, XY, +18) was used as the template, and 6 groups were set up in the study. Groups A and B were positive and negative control, respectively; groups C-F were experimental groups involving the MDA products from 1, 2, 5 and 10 cells respectively. In combination of single nucleotide polymorphism (SNP) array, the product of each group was assessed based on the genome coverage, loss of heterozygosity (LOH) rate and allele dropout (ADO) rate. Results The nonspecific product of negative control presented an average call rate of 3.2%. The genome coverage of the MDA product increased from 86.4% to 96.4% with the increasing number of template from 1 to 10 cells, while the LOH rate and ADO rate decreased significantly (P〈0. 05). Conclusion MDA is a highly efficient and reliable method for whole genome amplification. The fidelity of MDA will be improved significantly with the increasing number of template cells. 10K 2.0 SNP mapping array is a quick, accurate and comprehensive method to evaluate the fidelity of amplified DNA products, but the ADO SNPs should be distinguished from those of preferential amplification from the LOH loci to avoid errors.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2010年第1期42-46,共5页 Chinese Journal of Medical Genetics
基金 国家自然科学基金(30200301) 广东省自然科学基金(5001672,06021276) 广东省医学科学技术研究基金(B2006027)
关键词 单核苷酸多态性 单细胞 多重置换扩增 微阵列芯片 保真度 single nucleotide polymorphism single cell multiple displacement amplification microarray fidelity
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参考文献18

  • 1Peng W, Takabayashi H, Ikawa K. Whole genome amplification from single ceils in preimplantation genetic diagnosis and prenatal diagnosis. Eur J Obstet Gynecol Reprod Biol, 2007, 131:13- 20.
  • 2Handyside AH, Robinson MD, Simpson RJ, et al. Isothermal whole genome amplification from single and small numbers of cells:a new era for preimplantation genetic diagnosis of inherited disease. Mol HumReprod, 2004, 10:767-772.
  • 3Hellani A, Coskun S, Benkhalifa M, el al. Multiple displacement amplificalion on single cell and possible PGD applications. Mol HumReprod, 2004, 10:847- 8S2.
  • 4Panelli S, Damiani G, Espen L, et al. Towards the analysis of the genomes of single cells: further characterisation of the multiple displacement amplification. Gene, 2006, 372:1- 7.
  • 5Shoaib M, Baconnais S, Mechold U, et al. Multiple displacement amplification for complex mixtures of DNA fragments. BMC Genomics, 2008, 9 :415.
  • 6Hellani A, Abu-Amero K, Azouri J, et al. Pregnancy after preimplantation genetic diagnosis for brachydactyly type B. Reprod Biomed Online, 2009, 18:127-131.
  • 7Creary I.E, Girdlestone J, Zamora J, et al. Molecular typing of HLA genes using whole genome amplified DNA. Transfusion, 2009, 49:57-63.
  • 8Spits C, Le Caignee C, de Rycke M, et al. Optimization and evaluation of single cell whole genome multiple displacement amplification. Hun, Mutat, 2006, 27:496-503.
  • 9Ren Z, Zhou C, Xu Y, et al. Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification. Mol Hum Reprod, 2007, 13: 431-436.
  • 10Renwick PJ, Lewis CM, Abbs S, et al. Determination of the genetic status of cleavage-stage human embryos by microsatellite marker analysis following multiple displacement amplification. Prenat Diagn, 2007, 27:206-215.

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