Transcriptional and functional characterization in the terpenoid precursor pathway of the early land plant Physcomitrium patens.

IF 4.2 3区 生物学 Q1 PLANT SCIENCES Plant Biology Pub Date : 2024-11-27 DOI:10.1111/plb.13741
A Horn, Y Lu, F J Astorga Ríos, H Toft Simonsen, J D Becker
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Abstract

Isoprenoids comprise the largest group of plant specialized metabolites. 1-deoxy-D-xylulose-5-phosphate synthase (DXS) is one of the major rate-limiting enzymes in their biosynthesis. The DXS family expanded structurally and functionally during evolution and is believed to have significantly contributed to metabolic complexity and diversity in plants. This family has not yet been studied in Physcomitrium patens or other bryophytes. Here, we assessed the degree of evolutionary expansion in the DXS family in bryophytes and, more specifically, in P. patens using phylogenetic analysis. Transcriptome profiling was applied to investigate tissue-specific, developmental, and environmental responses, such as salt stress, in the DXS family. Moreover, the effect of salt stress on terpenoid biosynthesis was monitored through metabolomics. The phylogenetic analysis of DXS revealed that a structural expansion occurred in bryophytes, but not in P. patens. Functional complementation assay revealed functional activity in all four copies. Comparative transcriptomics showed tissue- and condition-specific divergence in the expression profiles of DXS copies and demonstrated specific stress responses for PpDXS1D, particularly to salt stress. These findings coincide with increased flux in the pathway towards downstream metabolites under salt stress. Additionally, co-expression network analysis revealed significant differences between the co-expressed genes of the DXS copies and illustrated enrichment of stress-responsive genes in the PpDXS1D network. These results suggest that the DXS family in P. patens is conserved but undergoes differential transcriptional regulation, which might allow P. patens to fine-tune DXS levels under different conditions, such as abiotic stress.

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早期陆生植物 Physcomitrium patens 的萜类前体途径的转录和功能特征。
异戊烯类化合物是植物专一代谢物中最大的一类。1-脱氧-D-木酮糖-5-磷酸合成酶(DXS)是其生物合成过程中的主要限速酶之一。在进化过程中,DXS 家族在结构和功能上都有所扩展,被认为极大地促进了植物代谢的复杂性和多样性。目前还没有人研究过该家族在斑叶树或其他叶绿体中的应用。在此,我们利用系统进化分析评估了 DXS 家族在石蒜科植物中的进化扩展程度,更具体地说,是在棒叶石蒜中的进化扩展程度。转录组分析被用于研究 DXS 家族的组织特异性、发育和环境反应,如盐胁迫。此外,还通过代谢组学监测了盐胁迫对萜类化合物生物合成的影响。DXS 的系统进化分析表明,其结构在叶绿体中发生了扩展,但在冬青叶绿体中却没有。功能互补分析表明所有四个拷贝都具有功能活性。比较转录组学显示,DXS拷贝的表达谱存在组织和条件特异性差异,并证明了 PpDXS1D 的特异性胁迫反应,尤其是对盐胁迫的反应。这些发现与盐胁迫下通向下游代谢物的通量增加相吻合。此外,共表达网络分析显示了 DXS 拷贝的共表达基因之间的显著差异,并说明了 PpDXS1D 网络中应激反应基因的富集。这些结果表明,青枯病菌中的 DXS 家族是保守的,但经历了不同的转录调控,这可能使青枯病菌在非生物胁迫等不同条件下对 DXS 水平进行微调。
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来源期刊
Plant Biology
Plant Biology 生物-植物科学
CiteScore
8.20
自引率
2.60%
发文量
109
审稿时长
3 months
期刊介绍: Plant Biology is an international journal of broad scope bringing together the different subdisciplines, such as physiology, molecular biology, cell biology, development, genetics, systematics, ecology, evolution, ecophysiology, plant-microbe interactions, and mycology. Plant Biology publishes original problem-oriented full-length research papers, short research papers, and review articles. Discussion of hot topics and provocative opinion articles are published under the heading Acute Views. From a multidisciplinary perspective, Plant Biology will provide a platform for publication, information and debate, encompassing all areas which fall within the scope of plant science.
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Transcriptional and functional characterization in the terpenoid precursor pathway of the early land plant Physcomitrium patens. Permeability of postzygotic barriers: embryology of a partially fertile Epidendrum (Orchidaceae) hybrid. Issue Information Modulatory responses of physiological and biochemical status are related to drought tolerance levels in peanut cultivars. Reduced soil moisture drives leaf anatomical shifts more than chronically elevated temperatures in European temperate trees.
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