大豆的共生结节分带和细胞分化由 NIN2 信号和 GH3 依赖性辅助素平衡决定

IF 10.7 1区 生物学 Q1 CELL BIOLOGY Developmental cell Pub Date : 2024-07-24 DOI:10.1016/j.devcel.2024.07.001
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引用次数: 0

摘要

共生结核包括两类,即不定芽和决定芽,由顶端分生组织和发育带的存在/不存在来定义。目前仍不清楚决定性节上为什么没有分生组织和发育带。在此,我们定义了发育中的大豆结节的细胞类型,强调了未分化感染区和分化固氮区。叶绿素控制感染区的维持GRETCHEN HAGEN 3(GH3)酶通过共轭作用使叶绿素失活,并促进细胞分化。中央共生转录因子 NIN2a 能激活 GH3.1,降低辅素水平,促进细胞分化。高浓度的植物生长素会促进 NIN2a 蛋白的积累并增强信号传导,从而进一步使植物生长素失活并减少感染区。我们的研究结果揭示了驱动大豆结节细胞分化的 NIN2a-GH3-a auxin 模块。这项研究挑战了我们对确定性结节发育的理解,并提出结节分带的调控为了解植物物种细胞分化的更广泛机制提供了宝贵的见解。
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Soybean symbiotic-nodule zonation and cell differentiation are defined by NIN2 signaling and GH3-dependent auxin homeostasis

Symbiotic nodules comprise two classes, indeterminate and determinate, defined by the presence/absence of apical meristem and developmental zonation. Why meristem and zonation are absent from determinate nodules remains unclear. Here, we define cell types in developing soybean nodules, highlighting the undifferentiated infection zones and differentiated nitrogen-fixation zones. Auxin governs infection zone maintenance. GRETCHEN HAGEN 3 (GH3) enzymes deactivate auxin by conjugation and promote cell differentiation. gh3 mutants increased undifferentiated cells and enlarged infection zones. The central symbiosis-transcription factor NIN2a activates GH3.1 to reduce auxin levels and facilitates cell differentiation. High auxin promotes NIN2a protein accumulation and enhances signaling, further deactivating auxin and depleting infection zones. Our findings shed light on the NIN2a-GH3-auxin module that drives soybean nodule cell differentiation. This study challenges our understanding of determinate nodule development and proposes that the regulation of nodule zonation offers valuable insights into broader mechanisms of cell differentiation across plant species.

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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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