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Intramembrane cleavage of AMA1 triggers Toxoplasma to switch from an invasive to a replicative mode

机译:AMA1的膜内切割触发弓形虫从侵入模式切换到复制模式

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摘要

Apicomplexan parasites invade host cells and immediately initiate cell division. The extracellular parasite discharges transmembrane proteins onto its surface to mediate motility and invasion. These are shed by intramembrane cleavage, a process associated with invasion but otherwise poorly understood. Functional analysis of Toxoplasma rhomboid 4, a surface intramembrane protease, by conditional overexpression of a catalytically inactive form produced a profound block in replication. This was completely rescued by expression of the cleaved cytoplasmic tail of Toxoplasma or Plasmodium apical membrane antigen 1 (AMA1). These results reveal an unexpected function for AMA1 in parasite replication and suggest that invasion proteins help to promote parasite switch from an invasive to a replicative mode.
机译:蚜虫寄生虫侵入宿主细胞并立即启动细胞分裂。细胞外寄生虫将跨膜蛋白释放到其表面上,以介导运动性和侵袭性。这些通过膜内分裂而脱落,该过程与侵入相关,但在其他方面了解甚少。通过有条件地过表达催化活性形式的菱形弓形虫4(一种表面膜内蛋白酶)的功能分析产生了一个深远的复制障碍。通过弓形虫或疟原虫顶端膜抗原1(AMA1)的裂解的细胞质尾巴的表达,可以完全挽救这一点。这些结果揭示了AMA1在寄生虫复制中具有意想不到的功能,并表明入侵蛋白有助于促进寄生虫从侵入模式向复制模式的转换。

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