Cyclophilin 20‐3 coordinates plant root hair growth and resistance against parasitic nematodes

IF 4.1 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Plant Science Pub Date : 2025-02-19 DOI:10.1016/j.plantsci.2025.112432
Simrandeep Kaur, Ashna Adhikari , Benjamin Welsh, Heather N. Gosse, Izailda Barbosa dos Santos, Wenshan Liu, Kathy S. Lawrence, Sang-Wook Park
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Abstract

Plant parasitic nematodes (PPN) are a major threat to agriculturally important crops, resulting in substantial yield losses and economic repercussions. However, the underlying modes of plant-PPN interactions remain largely elusive. Here, we describe a critical role of cyclophilin (CYP)20–3, a plastid dual enzyme [i.e., peptidyl-prolyl isomerase (PPIase) and reductase) in plant basal resistance against PPN attacks. Originally, in order to define a present working model of whether plant roots deploy hypersensitive response (HR) to restrict PPN infections, we co-imaged the ‘real-time’ interactions of a proposed HR system, cotton LONREN-1 vs. Rotylenchulus reniformis. The root imaginings, however, revealed no clear HR pattern, instead underpinning a negative relationship between PPN populations and extended root hair growth. The latter was then identified to couple with the spatial expression of PPIases, including homologs of CYP20‐3, a known receptor of 12-oxophytodienoic acid (OPDA) signal. To elaborate these findings further, we employed a reverse generic approach using a model plant Arabidopsis, and illuminated that knockout cyp20‐3 mutants i) abnormalize root hair formations and ii) enhance susceptibility to PPN, Meloidogyne hapla, challenges. Nevertheless, M. hapla infections did not induce OPDA synthesis and signaling marker gene expressions in Arabidopsis roots. In parallel, transgenic Arabidopsis plants overexpressing mutant CYP20‐3s defective OPDA-binding/signaling (H140Q) or PPIase (F74L) could still improve plant PPN defenses, whereas the overexpression of CYP20‐3C129S (−reductase) demonstrated WT-level galling formations. Thus, we conclude that OPDA-independent CYP20-3-reductase signaling plays a key role in the plant defense metabolic pathway, fortifying protective barriers and conferring innate resistance against PPN attacks.
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亲环蛋白20-3协调植物根毛生长和抵抗寄生线虫。
植物寄生线虫(PPN)是对重要农业作物的主要威胁,造成大量产量损失和经济影响。然而,植物与ppn相互作用的潜在模式在很大程度上仍然难以捉摸。在这里,我们描述了亲环蛋白(CYP)20-3,一种质体双酶[即肽基脯氨酸异构酶(PPIase)和还原酶)在植物对PPN攻击的基础抗性中的关键作用。最初,为了确定植物根系是否部署超敏反应(HR)来限制PPN感染的当前工作模型,我们共同成像了一个被提出的HR系统,棉花LONREN-1与肾形螺的“实时”相互作用。然而,根系想象没有显示出明确的HR模式,相反,PPN种群与延长的根毛生长之间存在负相关关系。随后发现后者与PPIases的空间表达偶联,包括CYP20-3的同源物,CYP20-3是一种已知的12-氧植物二烯酸(OPDA)信号受体。为了进一步阐明这些发现,我们采用了一种使用模式植物拟南芥的反向泛型方法,并阐明了敲除cyp20-3突变体i)使根毛形成异常,ii)增强对PPN (Meloidogyne hapla)挑战的易感性。然而,M. hapla感染并未诱导拟南芥根系中OPDA的合成和信号标记基因的表达。与此同时,转基因拟南芥植株过表达突变体CYP20-3s缺陷的opda结合/信号(H140Q)或PPIase (F74L)仍能提高植物对PPN的防御能力,而过表达CYP20-3C129S(-还原酶)则表现出wt水平的痛苦形成。因此,我们得出结论,不依赖opda的cyp20 -3还原酶信号在植物防御代谢途径中发挥关键作用,加强保护屏障并赋予对PPN攻击的先天抗性。
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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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