Evolutionary and biomedical implications of a Schistosoma japonicum complementary DNA resource

被引:256
作者
Hu, W
Yan, Q
Shen, DK
Liu, F
Zhu, ZD
Song, HD
Xu, XR
Wang, ZJ
Rong, YP
Zeng, LC
Wu, J
Zhang, X
Wang, JJ
Xu, XN
Wang, SY
Fu, G
Zhang, XL
Wang, ZQ
Brindley, PJ
McManus, DP
Xue, CL
Feng, Z
Chen, Z
Han, ZG
机构
[1] Chinese Natl Human Genome Ctr Shanghai, Shanghai 201203, Peoples R China
[2] Chinese Ctr Dis Control & Prevent, Inst Parasit Dis, Shanghai 200025, Peoples R China
[3] Shanghai Med Univ 2, Dept Parasitol, Shanghai 200025, Peoples R China
[4] Shanghai Med Univ 2, Rui Jin Hosp, State Key Lab Med Genom, Shanghai 200025, Peoples R China
[5] Tulane Univ, Hlth Sci Ctr, Dept Trop Med, New Orleans, LA 70112 USA
[6] Queensland Inst Med Res, Brisbane, Qld 4029, Australia
[7] Australian Ctr Int Hlth & Nutr, Brisbane, Qld 4029, Australia
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
D O I
10.1038/ng1236
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Schistosoma japonicum causes schistosomiasis in humans and livestock in the Asia-Pacific region. Knowledge of the genome of this parasite should improve understanding of schistosome-host interactions, biomedical aspects of schistosomiasis and invertebrate evolution. We assigned 43,707 expressed sequence tags ( ESTs) derived from adult S. japonicum and their eggs to 13,131 gene clusters. Of these, 35% shared no similarity with known genes and 75% had not been reported previously in schistosomes. Notably, S. japonicum encoded mammalian-like receptors for insulin, progesterone, cytokines and neuropeptides, suggesting that host hormones, or endogenous parasite homologs, could orchestrate schistosome development and maturation and that schistosomes modulate anti-parasite immune responses through inhibitors, molecular mimicry and other evasion strategies.
引用
收藏
页码:139 / 147
页数:9
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