Distinct domain regions of NIN and NLP1 mediate symbiotic and nitrate signalling in Medicago truncatula.

IF 5.7 2区 生物学 Q1 PLANT SCIENCES Journal of Experimental Botany Pub Date : 2025-05-27 DOI:10.1093/jxb/eraf037
Jiang Wang, Mengdi Fu, Zhenpeng Luo, Jing Liu, Fang Xie
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Abstract

Nodule Inception (NIN) and NIN-like protein 1 (NLP1), both belonging to the RWP-RK type transcription factors, play critical roles in plant development. Specifically, NIN is pivotal in facilitating root nodule symbiosis in nitrogen-starved conditions, while NLP1 coordinates nodulation in response to nitrate level. In this study, we conducted domain swapping experiments between NIN and NLP1 in Medicago truncatula to elucidate the functional significance of their respective domains. The findings reveal that the C-terminal regions, including the RWP-RK and PB1 domains of NIN, can substitute for those of NLP1, whereas reciprocal substitution does not yield equivalent outcomes. Moreover, our results emphasize the critical role of PB1-mediated interactions in the activity of NLP1, a feature not essential for NIN. Additionally, the N-terminal segment, conserved in NLPs but containing deletions or mutations in NIN, is essential for the proper functioning of both NIN and NLP1. Collectively, our research indicates evolutionary divergence of NIN from ancestral NLPs, suggesting specific adaptations that have enabled NIN as a central regulator in root nodulation processes.

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不同结构域的NIN和NLP1介导了苜蓿的共生和硝酸盐信号传导。
NIN和NIN样蛋白1 (NLP1)均属于RWP-RK型转录因子,在植物发育过程中起着至关重要的作用。具体来说,NIN在氮缺乏条件下促进根瘤共生至关重要,而NLP1则在硝酸盐水平下协调根瘤形成。在本研究中,我们进行了苜蓿中NIN和NLP1的结构域交换实验,以阐明其各自结构域的功能意义。研究结果表明,包括NIN的RWP-RK和PB1结构域在内的c端区域可以替代NLP1的结构域,而相互替代不能产生等效的结果。此外,我们的数据强调了pb1介导的相互作用对NLP1活性的关键作用,这对NIN来说不是必需的。此外,在nlp中保守但在NIN中含有缺失或突变的n端片段对于NIN和NLP1的正常功能至关重要。总的来说,我们的研究表明,NIN从祖先的nlp进化分化,表明特定的适应使NIN成为根结瘤过程的中心调节剂。
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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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