Microarray-based comparative genomic analyses of the human malaria parasite Plasmodium falciparum using Affymetrix arrays

被引:44
作者
Carret, CK
Horrocks, P
Konfortov, E
Winzeler, E
Qureshi, M
Newbold, C
Ivens, A
机构
[1] Wellcome Trust Sanger Inst, Pathogen Microarrays Grp, Cambridge CB10 1SA, England
[2] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Nuffield Dept Med,Mol Parasitol Grp, Oxford OX3 9DS, England
[3] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[4] Scripps Res Inst, La Jolla, CA USA
基金
英国惠康基金;
关键词
Plasmodium falciparum; chromosomal deletions; whole genome amplification; comparative genomic hybridization;
D O I
10.1016/j.molbiopara.2005.08.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microarray-based comparative genomic hybridization (CGH) provides a powerful tool for whole genome analyses and the rapid detection of genomic variation that underlies virulence and disease. In the field of Plasmodium research, many of the parasite genomes that one might wish to study in a high throughput manner are not laboratory clones, but clinical isolates. One of the key limitations to the use of clinical samples in CGH, however, is the miniscule amounts of genomic DNA available. Here we describe the successful application of multiple displacement amplification (MDA), a non-PCR-based amplification method that exhibits clear advantages over all other currently available methods. Using MDA, CGH was performed on a panel of NF54 and IT/FCR3 clones, identifying previously published deletions on chromosomes 2 and 9 as well as polymorphism in genes associated with disease pathology. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 186
页数:10
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