Effects of electron-beam irradiation on whole genome amplification

被引:14
作者
Bergen, AW
Qi, Y
Haque, KA
Welch, RA
Garcia-Closas, M
Chanock, SJ
Vaught, J
Castle, PE
机构
[1] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[2] NCI, Core Genotyping Facil, Ctr Adv Technol, Gaithersburg, MD USA
[3] NCI, Frederick Canc Res & Dev Ctr, Intramural Res Support Program, Sci Applicat Int Corp, Frederick, MD USA
[4] NCI, Canc Res Ctr, Pediat Oncol Branch, Bethesda, MD USA
关键词
D O I
10.1158/1055-9965.EPI-04-0686
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Electron-beam (E-beam) irradiation, currently being used to sterilize mail addressed to selected ZIP codes in the United States, has significant negative effects on the genomic integrity of DNA extracted from buccal-cell washes. We investigated the yield, composition, and genotyping performance of whole genome amplified DNA (wgaDNA) derived from 24 matched samples of E-beam-irradiated and nonirradiated genomic DNA (gDNA) as a model for the effects of degraded gDNA on the performance of whole genome amplification. gDNA was amplified using the Multiple Displacement Amplification method. Three methods of DNA quantification analysis were used to estimate the yield and composition of wgaDNA, and 65 short tandem repeat and single nucleotide polymorphism genotyping assays were used to evaluate the genotyping performance of irradiated and nonirradiated gDNA and wgaDNA. Compared with wgaDNA derived from nonirradiated gDNA, wgaDNA derived from irradiated gDNA exhibited a significantly reduced yield of wgaDNA and significantly reduced short tandem repeat and single nucleotide polymorphism genotyping completion and concordance rates (P < 0.0001). Increasing the amount of irradiated gDNA input into whole genome amplification improved genotyping performance of wgaDNA but not to the level of wgaDNA derived from nonirradiated gDNA. Multiple Displacement Amplification wgaDNA derived from E-beam-irradiated gDNA is not suitable for genotyping analysis.
引用
收藏
页码:1016 / 1019
页数:4
相关论文
共 12 条
[1]   Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel [J].
Barker, DL ;
Hansen, MST ;
Faruqi, AF ;
Giannola, D ;
Irsula, OR ;
Lasken, RS ;
Latterich, M ;
Makarov, V ;
Oliphant, A ;
Pinter, JH ;
Shen, R ;
Sleptsova, I ;
Ziehler, W ;
Lai, E .
GENOME RESEARCH, 2004, 14 (05) :901-907
[2]  
Boudaïffa B, 2000, SCIENCE, V287, P1658, DOI 10.1126/science.287.5458.1658
[3]   Effects of electron-beam irradiation on buccal-cell DNA [J].
Castle, PE ;
Garcia-Closas, M ;
Franklin, T ;
Chanock, S ;
Puri, V ;
Welch, R ;
Rothman, N ;
Vaught, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (03) :646-651
[4]  
García-Closas M, 2001, CANCER EPIDEM BIOMAR, V10, P687
[5]   Performance of high-throughput DNA quantification methods [J].
Haque, KA ;
Pfeiffer, RM ;
Beerman, MB ;
Struewing, JP ;
Chanock, SJ ;
Bergen, AW .
BMC BIOTECHNOLOGY, 2003, 3 (1)
[6]   Rubicon Genomics, Inc. [J].
Langmore, JP .
PHARMACOGENOMICS, 2002, 3 (04) :557-560
[7]   Whole genome amplification: abundant supplies of DNA from precious samples or clinical specimens [J].
Lasken, RS ;
Egholm, M .
TRENDS IN BIOTECHNOLOGY, 2003, 21 (12) :531-535
[8]  
Lizardi PM, 2000, US Patent, Patent No. [6124120, 6,124,120]
[9]   SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes [J].
Packer, BR ;
Yeager, M ;
Staats, B ;
Welch, R ;
Crenshaw, A ;
Kiley, M ;
Eckert, A ;
Beerman, M ;
Miller, E ;
Bergen, A ;
Rothman, N ;
Strausberg, R ;
Chanock, SJ .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D528-D532
[10]   Nanoscopic aspects of radiobiological damage: Fragmentation induced by secondary low-energy electrons [J].
Sanche, L .
MASS SPECTROMETRY REVIEWS, 2002, 21 (05) :349-369