Dupé Aurélien, Dumas Carole, Papadopoulou Barbara
Research Center in Infectious Diseases, CHU de Quebec Research Center-Université Laval and Department of Microbiology, Infectious Diseases and Immunology, Laval University, Quebec, QC, Canada.
PLoS One. 2015 Sep 3;10(9):e0137243. doi: 10.1371/journal.pone.0137243. eCollection 2015.
Alba-domain proteins are RNA-binding proteins found in archaea and eukaryotes and recently studied in protozoan parasites where they play a role in the regulation of virulence factors and stage-specific proteins. This work describes in silico structural characterization, cellular localization and biochemical analyses of Alba-domain proteins in Leishmania infantum. We show that in contrast to other protozoa, Leishmania have two Alba-domain proteins, LiAlba1 and LiAlba3, representative of the Rpp20- and the Rpp25-like eukaryotic subfamilies, respectively, which share several sequence and structural similarities but also important differences with orthologs in other protozoa, especially in sequences targeted for post-translational modifications. LiAlba1 and LiAlba3 proteins form a complex interacting with other RNA-binding proteins, ribosomal subunits, and translation factors as supported by co-immunoprecipitation and sucrose gradient sedimentation analysis. A higher co-sedimentation of Alba proteins with ribosomal subunits was seen upon conditions of decreased translation, suggesting a role of these proteins in translational repression. The Leishmania Alba-domain proteins display differential cellular localization throughout the parasite development. In the insect promastigote stage, Alba proteins co-localize predominantly to the cytoplasm but they translocate to the nucleolus and the flagellum upon amastigote differentiation in the mammalian host and are found back to the cytoplasm once amastigote differentiation is completed. Heat-shock, a major signal of amastigote differentiation, triggers Alba translocation to the nucleolus and the flagellum. Purification of the Leishmania flagellum confirmed LiAlba3 enrichment in this organelle during amastigote differentiation. Moreover, partial characterization of the Leishmania flagellum proteome of promastigotes and differentiating amastigotes revealed the presence of other RNA-binding proteins, as well as differences in the flagellum composition between these two parasite lifestages. Shuttling of Alba-domain proteins between the cytoplasm and the nucleolus or the flagellum throughout the parasite life cycle suggests that these RNA-binding proteins participate in several distinct regulatory pathways controlling developmental gene expression in Leishmania.
阿尔巴结构域蛋白是在古细菌和真核生物中发现的RNA结合蛋白,最近在原生动物寄生虫中进行了研究,它们在毒力因子和阶段特异性蛋白的调控中发挥作用。这项工作描述了婴儿利什曼原虫中阿尔巴结构域蛋白的计算机结构表征、细胞定位和生化分析。我们发现,与其他原生动物不同,利什曼原虫有两种阿尔巴结构域蛋白,LiAlba1和LiAlba3,分别代表Rpp20样和Rpp25样真核亚家族,它们具有一些序列和结构上的相似性,但与其他原生动物的直系同源物也有重要差异,特别是在翻译后修饰的靶向序列方面。LiAlba1和LiAlba3蛋白形成一个复合物,与其他RNA结合蛋白、核糖体亚基和翻译因子相互作用,这得到了免疫共沉淀和蔗糖梯度沉降分析的支持。在翻译减少的条件下,观察到阿尔巴蛋白与核糖体亚基的共沉降增加,表明这些蛋白在翻译抑制中起作用。利什曼原虫的阿尔巴结构域蛋白在寄生虫发育过程中表现出不同的细胞定位。在昆虫前鞭毛体阶段,阿尔巴蛋白主要共定位于细胞质,但在哺乳动物宿主中分化为无鞭毛体时,它们会转移到核仁和鞭毛上,一旦无鞭毛体分化完成,又会回到细胞质中。热休克是无鞭毛体分化的主要信号,它会触发阿尔巴蛋白转移到核仁和鞭毛上。利什曼原虫鞭毛的纯化证实了在无鞭毛体分化过程中LiAlba3在这个细胞器中的富集。此外,对前鞭毛体和分化中的无鞭毛体的利什曼原虫鞭毛蛋白质组的部分表征揭示了其他RNA结合蛋白的存在,以及这两个寄生虫生命周期阶段之间鞭毛组成的差异。在寄生虫生命周期中,阿尔巴结构域蛋白在细胞质与核仁或鞭毛之间穿梭,这表明这些RNA结合蛋白参与了控制利什曼原虫发育基因表达的几种不同调控途径。