放牧对转录组学的响应揭示了导致软骨藻酸生物合成的代谢途径,并强调了硅藻的不同防御策略

IF 2.946 Q3 Biochemistry, Genetics and Molecular Biology
Sara Harðardóttir, Sylke Wohlrab, Ditte Marie Hjort, Bernd Krock, Torkel Gissel Nielsen, Uwe John, Nina Lundholm
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引用次数: 22

摘要

浮游植物死亡的一个主要原因是浮游动物的捕食。避免食草动物的策略可能在浮游植物的进化中发挥了重要作用,并影响了水华动力学和营养能量运输。伪nitzschia属的某些物种产生神经毒素软骨藻酸(DA),作为对桡足类食草动物存在的反应,表明DA是一种防御化合物。DA的生物合成包括两种前体,C10类异戊二烯类香叶基焦磷酸和l-谷氨酸的融合。焦磷酸香叶醇(GPP)可能来自细胞质中的甲戊酸异戊二烯(MEV)途径或质体中的甲基赤四醇磷酸(MEP)途径。l-谷氨酸被认为来源于柠檬酸循环。Fragilariopsis是一种在系统发育上相关但无毒的硅藻属,似乎没有?类似的防御机制。我们获得了产毒性伪尼齐亚(pseudonitzschia seriata)合成、前体途径和DA产生调控功能相关基因的信息,以及硅藻对食草动物的反应相关基因的信息,以解决硅藻防御策略的共同反应。当假性nitzschia细胞暴露于捕食者信号时,有几个基因在细胞中表达。当处理相似时,Fragilariopsis中没有基因表达,这表明这两个分类群进化出了不同的策略来避免捕食。参与信号转导的基因表明,伪nitzschia细胞接收来自桡足动物的信号,这些信号转导级联分子前体导致DA的形成。在合成GPP的MEP途径中,7个基因中有5个基因上调,而在传统的MEV途径中没有上调。在DA形成的后期步骤中有五个已知或提示功能的基因被上调。我们的结论是,没有基因调控支持l-谷氨酸来源于柠檬酸循环,我们建议脯氨酸代谢为?做下游先驱。伪nitzschia细胞,而不是Fragilariopsis细胞,接受并响应桡足动物的信号。用于DA生物合成的C10类异戊二烯产物的细胞途径来自MEP代谢途径,我们认为脯氨酸代谢是l-谷氨酸的下游前体。我们认为13个功能未知的基因参与了硅藻对食草动物的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptomic responses to grazing reveal the metabolic pathway leading to the biosynthesis of domoic acid and highlight different defense strategies in diatoms

Transcriptomic responses to grazing reveal the metabolic pathway leading to the biosynthesis of domoic acid and highlight different defense strategies in diatoms

A major cause of phytoplankton mortality is predation by zooplankton. Strategies to avoid grazers have probably played a major role in the evolution of phytoplankton and impacted bloom dynamics and trophic energy transport. Certain species of the genus Pseudo-nitzschia produce the neurotoxin, domoic acid (DA), as a response to the presence of copepod grazers, suggesting that DA is a defense compound. The biosynthesis of DA comprises fusion of two precursors, a C10 isoprenoid geranyl pyrophosphate and l-glutamate. Geranyl pyrophosphate (GPP) may derive from the mevalonate isoprenoid (MEV) pathway in the cytosol or from the methyl-erythritol phosphate (MEP) pathway in the plastid. l-glutamate is suggested to derive from the citric acid cycle. Fragilariopsis, a phylogenetically related but nontoxic genus of diatoms, does not appear to possess a?similar defense mechanism. We acquired information on genes involved in biosynthesis, precursor pathways and regulatory functions for DA production in the toxigenic Pseudo-nitzschia seriata, as well as genes involved in responses to grazers to resolve common responses for defense strategies in diatoms.

Several genes are expressed in cells of Pseudo-nitzschia when these are exposed to predator cues. No genes are expressed in Fragilariopsis when treated similarly, indicating that the two taxa have evolved different strategies to avoid predation. Genes involved in signal transduction indicate that Pseudo-nitzschia cells receive signals from copepods that transduce cascading molecular precursors leading to the formation of DA. Five out of seven genes in the MEP pathway for synthesis of GPP are upregulated, but none in the conventional MEV pathway. Five genes with known or suggested functions in later steps of DA formation are upregulated. We conclude that no gene regulation supports that l-glutamate derives from the citric acid cycle, and we suggest the proline metabolism to?be a downstream precursor.

Pseudo-nitzschia cells, but not Fragilariopsis, receive and respond to copepod cues. The cellular route for the C10 isoprenoid product for biosynthesis of DA arises from the MEP metabolic pathway and we suggest proline metabolism to be a downstream precursor for l-glutamate. We suggest 13 genes with unknown function to be involved in diatom responses to grazers.

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来源期刊
BMC Molecular Biology
BMC Molecular Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Molecular Biology is an open access journal publishing original peer-reviewed research articles in all aspects of DNA and RNA in a cellular context, encompassing investigations of chromatin, replication, recombination, mutation, repair, transcription, translation and RNA processing and function.
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