Laboratorio de Parasitología Molecular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia; Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma de Madrid, Madrid, Spain.
Centro de Biología Molecular Severo Ochoa (CSIC-UAM), Universidad Autónoma de Madrid, Madrid, Spain.
J Proteomics. 2021 Feb 20;233:104066. doi: 10.1016/j.jprot.2020.104066. Epub 2020 Dec 6.
Leishmania are protozoan parasites responsible for leishmaniasis. These parasites present a precise gene regulation that allows them to survive different environmental conditions during their digenetic life cycle. This adaptation depends on the regulation of the expression of a wide variety of genes, which occurs, mainly at the post-transcriptional level. This differential gene expression is achieved by mechanisms based mainly in RNA binding proteins that regulate the translation and/or stability of mRNA targets by interaction with cis elements principally located in the untranslated regions (UTR). In recent studies, our group identified and characterized two proteins, SCD6 and RBP42, as RNA binding proteins in Leishmania braziliensis. To find clues about the cellular processes in which these proteins are involved, this work was aimed to determine the SCD6- and RBP42-interacting proteins (interactome) in L. braziliensis promastigotes. For this purpose, after an in vivo UV cross-linking, cellular extracts were used to immunoprecipitated, by specific antibodies, protein complexes in which SCD6 or RBP42 were present. Protein mass spectrometry analysis of the immunoprecipitated proteins identified 96 proteins presumably associated with SCD6 and 173 proteins associated with RBP42. Notably, a significant proportion of the identified proteins were shared in both interactomes, indicating a possible functional relationship between SCD6 and RBP42. Remarkably, many of the proteins identified in the SCD6 and RBP42 interactomes are related to RNA metabolism and translation processes, and many of them have been described as components of ribonucleoprotein (RNP) granules in Leishmania and related trypanosomatids. Thus, these results support a role of SCD6 and RBP42 in the assembly and/or function of mRNA-protein complexes, participating in the fate (decay/accumulation/translation) of L. braziliensis transcripts. SIGNIFICANCE: Parasites of the Leishmania genus present a particular regulation of gene expression, operating mainly at the post-transcriptional level, surely aimed to modulate quickly both mRNA and protein levels to survive the sudden environmental changes that occur during a parasite's life cycle as it moves from one host to another. This regulation of gene expression processes would be governed by the interaction of mRNA with RNA binding proteins. Nevertheless, the entirety of protein networks involved in these regulatory processes is far from being understood. In this regard, our work is contributing to stablish protein networks in which the L. braziliensis SCD6 and RBP42 proteins are involved; these proteins, in previous works, have been described as RNA binding proteins and found to participate in gene regulation in different cells and organisms. Additionally, our data point out a possible functional relationship between SCD6 and RBP42 proteins as constituents of mRNA granules, like processing bodies or stress granules, which are essential structures in the regulation of gene expression. This knowledge could provide a new approach for the development of therapeutic targets to control Leishmania infections.
利什曼原虫是一种引起利什曼病的原生动物寄生虫。这些寄生虫具有精确的基因调控机制,使它们能够在双态生命周期中生存于不同的环境条件下。这种适应依赖于广泛的基因表达调控,主要发生在转录后水平。这种差异基因表达是通过主要基于 RNA 结合蛋白的机制实现的,这些蛋白通过与主要位于非翻译区 (UTR) 的顺式元件相互作用来调节 mRNA 靶标的翻译和/或稳定性。在最近的研究中,我们的小组在巴西利什曼原虫中鉴定并表征了两种蛋白质,SCD6 和 RBP42,作为 RNA 结合蛋白。为了找到这些蛋白质参与的细胞过程的线索,这项工作旨在确定巴西利什曼原虫前鞭毛体中 SCD6 和 RBP42 的相互作用蛋白(相互作用组)。为此,在体内 UV 交联后,使用特定抗体从细胞提取物中免疫沉淀存在 SCD6 或 RBP42 的蛋白复合物。对免疫沉淀蛋白进行蛋白质质谱分析,鉴定了 96 种可能与 SCD6 相关的蛋白和 173 种与 RBP42 相关的蛋白。值得注意的是,两个相互作用组中都有很大一部分鉴定出的蛋白是共享的,表明 SCD6 和 RBP42 之间可能存在功能关系。值得注意的是,在 SCD6 和 RBP42 相互作用组中鉴定出的许多蛋白与 RNA 代谢和翻译过程有关,其中许多蛋白已被描述为利什曼原虫和相关的锥虫中核糖核蛋白 (RNP) 颗粒的组成部分。因此,这些结果支持 SCD6 和 RBP42 在 mRNA-蛋白复合物的组装和/或功能中的作用,参与巴西利什曼原虫转录物的命运(降解/积累/翻译)。意义:利什曼属寄生虫的基因表达存在特定的调控,主要发生在转录后水平,肯定是为了快速调节 mRNA 和蛋白质水平,以适应寄生虫生命周期中从一个宿主到另一个宿主时发生的环境变化。这种基因表达调控过程将受到 mRNA 与 RNA 结合蛋白相互作用的控制。然而,参与这些调节过程的蛋白质网络的全貌还远未被理解。在这方面,我们的工作有助于建立涉及巴西利什曼原虫 SCD6 和 RBP42 蛋白的蛋白质网络;在之前的工作中,这些蛋白被描述为 RNA 结合蛋白,并发现它们参与不同细胞和生物体的基因调控。此外,我们的数据指出 SCD6 和 RBP42 蛋白作为 mRNA 颗粒(如加工体或应激颗粒)的组成部分之间可能存在功能关系,这些颗粒是基因表达调控的重要结构。这一知识可能为开发治疗利什曼感染的新靶点提供新方法。