Malaria Unit, Instituto de Medicina Molecular, Lisboa, Portugal.
PLoS Pathog. 2011 May;7(5):e1002046. doi: 10.1371/journal.ppat.1002046. Epub 2011 May 19.
Many eukaryotic developmental and cell fate decisions that are effected post-transcriptionally involve RNA binding proteins as regulators of translation of key mRNAs. In malaria parasites (Plasmodium spp.), the development of round, non-motile and replicating exo-erythrocytic liver stage forms from slender, motile and cell-cycle arrested sporozoites is believed to depend on environmental changes experienced during the transmission of the parasite from the mosquito vector to the vertebrate host. Here we identify a Plasmodium member of the RNA binding protein family PUF as a key regulator of this transformation. In the absence of Pumilio-2 (Puf2) sporozoites initiate EEF development inside mosquito salivary glands independently of the normal transmission-associated environmental cues. Puf2- sporozoites exhibit genome-wide transcriptional changes that result in loss of gliding motility, cell traversal ability and reduction in infectivity, and, moreover, trigger metamorphosis typical of early Plasmodium intra-hepatic development. These data demonstrate that Puf2 is a key player in regulating sporozoite developmental control, and imply that transformation of salivary gland-resident sporozoites into liver stage-like parasites is regulated by a post-transcriptional mechanism.
许多真核生物的发育和细胞命运决定是通过 RNA 结合蛋白作为关键 mRNA 翻译的调节剂来实现的。在疟原虫(Plasmodium spp.)中,从细长的、运动的和细胞周期停滞的子孢子发育为圆形的、非运动的和复制的外红细胞期形式,被认为依赖于寄生虫从蚊子媒介传播到脊椎动物宿主过程中经历的环境变化。在这里,我们确定了 RNA 结合蛋白家族 PUF 的一个疟原虫成员是这种转化的关键调节剂。在没有 Pumilio-2(Puf2)的情况下,子孢子在蚊子唾液腺中独立于正常的与传播相关的环境线索开始 EEF 发育。Puf2-子孢子表现出全基因组转录变化,导致滑行运动、细胞穿透能力丧失和感染力降低,而且,还引发典型的早期疟原虫肝内发育的变态。这些数据表明,Puf2 是调节子孢子发育控制的关键因素,并暗示唾液腺驻留的子孢子向肝期样寄生虫的转化是由转录后机制调节的。