地衣光生物Trebouxia属的成员对强光表现出物种特异性的光生理和转录组水平的反应。

IF 5.7 2区 生物学 Q1 PLANT SCIENCES
Rosa Celia Poquita-Du, Jürgen Otte, Nicolas Herrmann, Claudia Büchel, Imke Schmitt
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引用次数: 0

摘要

从北极到热带,常见的光生地衣Trebouxia成员存在于所有陆地栖息地,然而,Trebouxia对环境胁迫的耐受机制知之甚少。目前,该属的谱系被划分为A、C、I、S、d支系。本文研究了从地衣形成真菌脐藻和U. phaea中分离出来的6种,分别属于Trebouxia的S支系和A支系。其中3种在低海拔(地中海气候)有气候生态位偏好,2种在高海拔(寒温带气候)有气候生态位偏好,1种在两个气候带都有。这些物种表现出广泛的基因组差异,特别是在与光合作用相关的基因组区域。因此,我们假设它们在不同的光照条件下会表现出不同的性能。我们使用受控环境室评估了对高光(HL)(对照组:60µmol光子/m2/s; HL:150µmol光子/m2/s)的生理和转录组反应。我们检测了HL暴露1小时和3天(每天12小时)后培养物的反应。我们测量了光生理参数,包括最大量子产率(Fv/Fm)、非光化学猝灭(NPQ)和叶绿素a (chl a)浓度,并通过RNASeq进行差异基因表达分析。暴露于HL后,Fv/Fm和NPQ的平均水平显著降低,但不同物种之间存在差异。高海拔种(即Trebouxia S12 C0006和A10 C0009)在整个实验过程中表现出较高的NPQ能力。平均chl - a浓度无显著变化。此外,在暴露于HL 1小时后,只有少数差异表达基因(DEGs)在特定物种中被发现,包括与叶绿体类囊体膜、转座子TX1和光呼吸相关的基因。另一方面,暴露于长时间HL环境下的所有Trebouxia物种都有更多的deg,这些deg涉及与DNA生物合成过程、细胞周期和细胞壁组织相关的基因。与NPQ、光系统II修复、出氧组装和光保护色素(类胡萝卜素和chl)的生物合成相关的光保护相关基因也因长期HL而表现出差异表达。总的来说,我们的研究结果表明,在Trebouxia中,承受强光条件的能力是高度物种特异性的,而不是由系统发育相关性或气候生态位偏好驱动的。除了高海拔地区(Trebouxia S12 C0006和A10 C0009)的物种表现出较高的NPQ能力外,我们没有观察到其他物种对相似气候生态位的偏好相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Members of the lichen photobiont genus Trebouxia show species-specific photo-physiological and transcriptome-level responses to high light.

Members of the common lichen photobiont Trebouxia occur in all terrestrial habitats, from the arctic to the tropics, however, the mechanisms of environmental stress tolerance in Trebouxia are little understood. Currently, lineages belonging to this genus are grouped into clades A, C, I, S, D. Here we study six species, which belong to the S-Clade and A-Clade of Trebouxia, and were isolated from the lichen-forming fungi Umbilicaria pustulata and U. phaea. Three of the Trebouxia species have a climatic niche preference at low elevation (Mediterranean climate), two at high elevation (cold temperate climate), and one is found in both climate zones. These species have demonstrated extensive genomic divergence, particularly in genome regions associated with photosynthesis. Therefore, we hypothesize that they will exhibit differential performance under varying light conditions. We assessed physiological and transcriptomic responses to high light (HL) (control: 60 µmol photons/m2/s; HL:150 µmol photons/m2/s) using a controlled environmental chamber. We examined the cultures´ responses after 1 hour and 3 days (12 hours per day) of HL exposure. We measured photo-physiological parameters including maximum quantum yield (Fv/Fm), non-photochemical quenching (NPQ) and chlorophyll a (chl a) concentration in combination with differential gene expression analysis via RNASeq. Average levels of Fv/Fm and NPQ showed significant reduction following HL exposure, however, this varied among species. Species from high elevation (i.e. Trebouxia S12 C0006 and A10 C0009) exhibited relatively high NPQ capacity throughout the experiment. There was no significant change in average chl a concentration. Further, only a few differentially expressed genes (DEGs) were found for specific species following exposure to 1 hour HL, including those associated with chloroplast thylakoid membrane, transposon TX1 and photorespiration. On the other hand, there are more DEGs found for all Trebouxia species exposed to prolonged HL, which involved genes associated to DNA biosynthetic process, cell cycle and cell wall organization. Photoprotection-associated genes related to NPQ, photosystem II repair, oxygen evolving assembly and biosynthesis of photoprotective pigments (carotenoid and chl) also showed differential expression due to prolonged HL. Overall, our findings show that in Trebouxia the capacity to withstand high light conditions is highly species-specific, and not driven by phylogenetic relatedness, or climatic niche preference. We do not observe parallel patterns in species preferring similar climatic niches, with the exception of species from high elevation (Trebouxia S12 C0006 and A10 C0009), which exhibit generally high NPQ capacity.

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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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