Laboratório de Ciclo Celular, Instituto Butantan, São Paulo, SP, Brazil; Center of Toxins, Immune Response and Cell Signaling (CeTICS), Instituto Butantan, São Paulo, SP, Brazil.
Laboratório de Ciclo Celular, Instituto Butantan, São Paulo, SP, Brazil; Center of Toxins, Immune Response and Cell Signaling (CeTICS), Instituto Butantan, São Paulo, SP, Brazil; Instituto Carlos Chagas, FIOCRUZ, Rua Algacyr Munhoz Mader, 3775. CIC, Curitiba, PR 81350-010, Brazil.
J Proteomics. 2020 Aug 15;225:103847. doi: 10.1016/j.jprot.2020.103847. Epub 2020 May 29.
Trypanosome histone N-terminal sequences are very divergent from the other eukaryotes, although they are still decorated by post-translational modifications (PTMs). Here, we used a highly robust workflow to analyze histone PTMs in the parasite Trypanosoma cruzi using mass spectrometry-based (MS-based) data-independent acquisition (DIA). We adapted the workflow for the analysis of the parasite's histone sequences by modifying the software EpiProfile 2.0, improving peptide and PTM quantification accuracy. This workflow could now be applied to the study of 141 T. cruzi modified histone peptides, which we used to investigate the dynamics of histone PTMs along the metacyclogenesis and the life cycle of T. cruzi. Global levels of histone acetylation and methylation fluctuates along metacyclogenesis, however most critical differences were observed between parasite life forms. More than 66 histone PTM changes were detected. Strikingly, the histone PTM pattern of metacyclic trypomastigotes is more similar to epimastigotes than to cellular trypomastigotes. Finally, we highlighted changes at the H4 N-terminus and at H3K76 discussing their impact on the trypanosome biology. Altogether, we have optimized a workflow easily applicable to the analysis of histone PTMs in T. cruzi and generated a dataset that may shed lights on the role of chromatin modifications in this parasite. SIGNIFICANCE: Trypanosomes are unicellular parasites that have divergent histone sequences, no chromosome condensation and a peculiar genome/gene regulation. Genes are transcribed from divergent polycistronic regions and post-transcriptional gene regulation play major role on the establishment of transcripts and protein levels. In this regard, the fact that their histones are decorated with multiple PTMs raises interesting questions about their role. Besides, this digenetic organism must adapt to different environments changing its metabolism accordingly. As metabolism and epigenetics are closely related, the study of histone PTMs in trypanosomes may enlighten this strikingly, and not yet fully understood, interplay. From a biomedical perspective, the comprehensive study of molecular mechanisms associated to the metacyclogenesis process is essential to create better strategies for controlling Chagas disease.
锥虫组蛋白 N 端序列与其他真核生物非常不同,尽管它们仍然被翻译后修饰(PTMs)所修饰。在这里,我们使用一种高度稳健的工作流程,使用基于质谱的(MS 基础)数据独立采集(DIA)来分析寄生虫克鲁兹锥虫中的组蛋白 PTM。我们通过修改软件 EpiProfile 2.0 来适应寄生虫组蛋白序列的分析,从而提高肽和 PTM 定量的准确性。现在,这个工作流程可以应用于 141 个克鲁兹锥虫修饰组蛋白肽的研究,我们用它来研究组蛋白 PTM 在克鲁兹锥虫的外生体和生命周期中的动态变化。组蛋白乙酰化和甲基化的整体水平在外生体发生过程中波动,但在寄生虫的生命形式之间观察到了最关键的差异。检测到超过 66 个组蛋白 PTM 变化。引人注目的是,外生体锥虫的组蛋白 PTM 模式与锥鞭毛体更相似,而与细胞质锥虫更不相似。最后,我们强调了 H4 N 端和 H3K76 的变化,讨论了它们对锥虫生物学的影响。总之,我们优化了一个工作流程,易于应用于克鲁兹锥虫组蛋白 PTM 的分析,并生成了一个数据集,可能有助于了解染色质修饰在这种寄生虫中的作用。意义:锥虫是单细胞寄生虫,它们的组蛋白序列具有差异性,没有染色体浓缩,并且具有特殊的基因组/基因调控。基因从不同的多顺反子区域转录,转录后基因调控在建立转录物和蛋白质水平方面发挥着主要作用。在这方面,它们的组蛋白被多种 PTM 修饰这一事实引发了关于它们作用的有趣问题。此外,这种双核生物必须适应不同的环境,相应地改变其新陈代谢。由于新陈代谢和表观遗传学密切相关,因此研究锥虫中的组蛋白 PTM 可能会阐明这一尚未完全理解的相互作用。从生物医学的角度来看,全面研究与外生体发生过程相关的分子机制对于制定更好的控制恰加斯病的策略至关重要。