首页> 美国卫生研究院文献>PLoS Pathogens >Epigenetic Silencing of Plasmodium falciparum Genes Linked to Erythrocyte Invasion
【2h】

Epigenetic Silencing of Plasmodium falciparum Genes Linked to Erythrocyte Invasion

机译:与红细胞入侵有关的恶性疟原虫基因的表观遗传沉默

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

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.
机译:恶性疟原虫裂殖子入侵红细胞的过程涉及多个步骤,包括在寄生虫和宿主细胞之间形成活动连接,并且其特征在于涉及的许多受体-配体相互作用是多余的。与红细胞受体相互作用或参与其他侵袭步骤的几种寄生虫蛋白由位于4至7个成员的亚端粒小基因家族编码。我们在这里报告,eba,rhoph1 / clag,acbp和pfRh多基因家族的成员以活跃或沉默的状态存在。对于rhoph1 / clag家族的两个成员clag3.1和clag3.2,表达是互斥的。沉默是克隆传播的,并且在没有可检测的DNA改变的情况下发生,表明它是表观遗传的。 eba-140对此进行了演示。我们的数据表明,疟原虫中的变体或互斥表达和表观遗传沉默不是诸如var这样的基因所特有的,var编码输出到红细胞表面的蛋白质,但对于参与宿主细胞入侵的基因也会发生这种情况。入侵相关配体的克隆变异表达增加了寄生虫适应其人类宿主的灵活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号