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Epigenetic silencing of plasmodium falciparum genes linked to erythrocyte invasion
被引:115
作者:
Cortes, Alfred
Carret, Celine
Kaneko, Osamu
Lim, Brian Y. S. Yim
Ivens, Alasdair
Holder, Anthony A.
机构:
[1] Med Res Council Natl Inst Med Res, Div Parasitol, London, England
[2] ICREA, IRB, Barcelona, Spain
[3] Wellcome Trust Sanger Inst, Pathogen Microarray Grp, Cambridge, England
[4] Ehime Univ, Sch Med, Dept Mol Parasitol, Matsuyama, Ehime 790, Japan
基金:
英国医学研究理事会;
英国惠康基金;
关键词:
D O I:
10.1371/journal.ppat.0030107
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The process of erythrocyte invasion by merozoites of Plasmodium falciparum involves multiple steps, including the formation of a moving junction between parasite and host cell, and it is characterised by the redundancy of many of the receptor-ligand interactions involved. Several parasite proteins that interact with erythrocyte receptors or participate in other steps of invasion are encoded by small subtelomerically located gene families of four to seven members. We report here that members of the eba, rhoph1/clag, acbp, and pfRh multigene families exist in either an active or a silenced state. In the case of two members of the rhoph1/clag family, clag3.1 and clag3.2, expression was mutually exclusive. Silencing was clonally transmitted and occurred in the absence of detectable DNA alterations, suggesting that it is epigenetic. This was demonstrated for eba-140. Our data demonstrate that variant or mutually exclusive expression and epigenetic silencing in Plasmodium are not unique to genes such as var, which encode proteins that are exported to the surface of the erythrocyte, but also occur for genes involved in host cell invasion. Clonal variant expression of invasion-related ligands increases the flexibility of the parasite to adapt to its human host.
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页码:1023 / 1035
页数:13
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