Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Curr Genomics. 2010 Jun;11(4):279-86. doi: 10.2174/138920210791233081.
With the completion and near completion of many malaria parasite genome-sequencing projects, efforts are now being directed to a better understanding of gene functions and to the discovery of vaccine and drug targets. Inter- and intraspecies comparisons of the parasite genomes will provide invaluable insights into parasite evolution, virulence, drug resistance, and immune invasion. Genome-wide searches for loci under various selection pressures may lead to discovery of genes conferring drug resistance or encoding for protective antigens. In addition, the Plasmodium falciparum genome sequence provides the basis for the development of various microarrays to monitor gene expression and to detect nucleotide substitution and deletion/amplification. Genome-wide profiling of the parasite proteome, chromatin modification, and nucleosome position also depend on availability of the parasite genome. In this brief review, we will highlight some recent advances and studies in characterizing gene function and related phenotype in P. falciparum that were made possible by the genome sequence, particularly the development of a genome-wide diversity map and various high-throughput genotyping methods for genome-wide association studies (GWAS).
随着许多疟原虫基因组测序项目的完成和接近完成,目前的工作重点是更好地了解基因功能,并发现疫苗和药物靶点。寄生虫基因组的种间和种内比较将为寄生虫进化、毒力、药物抗性和免疫入侵提供宝贵的见解。对各种选择压力下的基因座进行全基因组搜索,可能会发现赋予药物抗性或编码保护性抗原的基因。此外,恶性疟原虫基因组序列为开发各种微阵列提供了基础,用于监测基因表达以及检测核苷酸替换和缺失/扩增。寄生虫蛋白质组、染色质修饰和核小体位置的全基因组分析也依赖于寄生虫基因组的可用性。在这篇简要综述中,我们将重点介绍一些最近的进展和研究,这些进展和研究通过基因组序列来描述恶性疟原虫中的基因功能和相关表型,特别是开发了全基因组多样性图谱和各种高通量基因分型方法,用于全基因组关联研究(GWAS)。