Schistosoma mansoni genome project:: an update

被引:41
作者
LoVerde, PT [1 ]
Hirai, H
Merrick, JM
Lee, NH
El-Sayed, N
机构
[1] SUNY Buffalo, Dept Microbiol & Immunol, Buffalo, NY 14214 USA
[2] Kyoto Univ, Primate Res Inst, Inuyama, Aichi 4848506, Japan
[3] Inst Genom Res, Dept Funct Genom, Rockville, MD 20850 USA
[4] George Washington Univ, Dept Microbiol & Trop Med, Washington, DC 20037 USA
[5] Inst Genom Res, Dept Parasite Genom, Rockville, MD 20850 USA
关键词
Schistosoma mansoni; genomics; gene discovery; chromosome mapping;
D O I
10.1016/j.parint.2004.01.009
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
A schistosome genome project was initiated by the World Health Organization in 1994 with the notion that the best prospects for identifying new targets for drugs, vaccines, and diagnostic development lie in schistosome gene discovery, development of chromosome maps, whole genome sequencing and genome analysis. Schistosoma mansoni has a haploid genome of 270 Mb contained on 8 pairs of chromosomes. It is estimated that the S. mansoni genome contains between 15 000 and 25 000 genes. There are approximately 16 689 ESTs obtained from diverse libraries representing different developmental stages of S. mansoni, deposited in the NCB1 EST database. More than half of the deposited sequences correspond to genes of unknown function. Approximately 40-50% of the sequences form unique clusters, suggesting that approximately 20-25% of the total schistosome genes have been discovered. Efforts to develop low resolution chromosome maps are in progress. There is a genome sequencing program underway that will provide 3X sequence coverage of the S. mansoni genome that will result in approximately 95% gene discovery. The genomics era has provided the resources to usher in the era of functional genomics that will involve microarrays to focus on specific metabolic pathways, proteomics to identify relevant proteins and protein-protein interactions to understand critical parasite pathways. Functional genomics is expected to accelerate the development of control and treatment strategies for schistosomiasis. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:183 / 192
页数:10
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