Life Science Research Centre, Department of Biology and Ecology and Institute of Environmental Technologies, Faculty of Science, University of Ostrava, 701 00, Ostrava, Czech Republic.
Institute of Parasitology, Biology Centre CAS, 370 05, České Budějovice, Czech Republic.
Sci Rep. 2018 Nov 19;8(1):17012. doi: 10.1038/s41598-018-35389-1.
Euglenophytes are a familiar algal group with green alga-derived secondary plastids, but the knowledge of euglenophyte plastid function and evolution is still highly incomplete. With this in mind we sequenced and analysed the transcriptome of the non-photosynthetic species Euglena longa. The transcriptomic data confirmed the absence of genes for the photosynthetic machinery, but provided candidate plastid-localised proteins bearing N-terminal bipartite topogenic signals (BTSs) of the characteristic euglenophyte type. Further comparative analyses including transcriptome assemblies available for photosynthetic euglenophytes enabled us to unveil salient aspects of the basic euglenophyte plastid infrastructure, such as plastidial targeting of several proteins as C-terminal translational fusions with other BTS-bearing proteins or replacement of the conventional eubacteria-derived plastidial ribosomal protein L24 by homologs of archaeo-eukaryotic origin. Strikingly, no homologs of any key component of the TOC/TIC system and the plastid division apparatus are discernible in euglenophytes, and the machinery for intraplastidial protein targeting has been simplified by the loss of the cpSRP/cpFtsY system and the SEC2 translocon. Lastly, euglenophytes proved to encode a plastid-targeted homolog of the termination factor Rho horizontally acquired from a Lambdaproteobacteria-related donor. Our study thus further documents a substantial remodelling of the euglenophyte plastid compared to its green algal progenitor.
眼虫是一种常见的藻类群体,具有源自绿藻的次生质体,但对眼虫质体功能和进化的了解仍然非常不完整。考虑到这一点,我们对非光合物种长眼虫的转录组进行了测序和分析。转录组数据证实了缺乏光合作用机制的基因,但提供了候选质体定位蛋白,这些蛋白具有特征性眼虫类型的 N 端双部分靶向信号 (BTS)。进一步的比较分析,包括可用于光合眼虫的转录组组装,使我们能够揭示基本眼虫质体基础设施的显著方面,例如几种蛋白质的质体靶向作为与其他带有 BTS 的蛋白质的 C 端翻译融合,或用古真核生物起源的同源物替代传统的细菌衍生的质体核糖体蛋白 L24。值得注意的是,在眼虫中无法识别 TOC/TIC 系统和质体分裂装置的任何关键组成部分的同源物,并且质体内部蛋白质靶向的机制已经通过 cpSRP/cpFtsY 系统和 SEC2 转运蛋白的丢失而简化。最后,眼虫被证明编码了一种源自 Lambdaproteobacteria 相关供体的终止因子 Rho 的质体靶向同源物。因此,我们的研究进一步证明了与绿藻祖先相比,眼虫质体发生了实质性的重塑。