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CLAVATA3不敏感受体激酶调控拟南芥侧根的起始与间距。

CLAVATA3 INSENSITIVE RECEPTOR KINASEs regulate lateral root initiation and spacing in Arabidopsis.

作者信息

Meng Xianghu, Ye Rui, Cao Jing, Tao Liang, Wang Zhe, Kong Tianzhen, Hu Chong, Yi Jing, Gou Xiaoping

机构信息

Ministry of Education Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University, Lanzhou 730000, China.

出版信息

Plant Physiol. 2024 Dec 23;197(1). doi: 10.1093/plphys/kiae540.

Abstract

The root system architecture is very critical for plants to adapt to ever-changing environmental stimulations and is largely affected by lateral roots (LRs). Therefore, how plants regulate LR initiation and spacing is a key point for root system development. Previous studies have shown that RECEPTOR-LIKE KINASE 7 (RLK7) and its ligand TARGET OF LBD SIXTEEN 2 (TOLS2) control the initiation and spacing of LRs. However, the molecular mechanism underlying the perception and transduction of the TOLS2 signal by RLK7 remains to be elucidated. In this study, we explored whether CLAVATA3 INSENSITIVE RECEPTOR KINASEs (CIKs) are critical signaling components during Arabidopsis (Arabidopsis thaliana) LR development by investigating phenotypes of cik mutants and examining interactions between CIKs and members of the RLK7-mediated signaling pathway. Our results showed that high-order cik mutants generated more LRs because of more LR initiation and defective LR spacing. The cik mutants showed reduced sensitivity to applied TOLS2 peptides. TOLS2 application enhanced the interactions between CIKs and RLK7 and the RLK7-dependent phosphorylation of CIKs. In addition, overexpression of transcription factor PUCHI and constitutive activation of MITOGEN-ACTIVATED PROTEIN KINASE KINASE 4 (MKK4) and MKK5 partially rescued the spacing defects of LRs in cik and rlk7-3 mutants. Moreover, we discovered that auxin maximum in pericycle cells altered subcellular localization of CIKs to determine lateral root founder cells. These findings revealed that CIKs and RLK7 function together to perceive the TOLS2 signal and regulate LR initiation and spacing through the MKK4/5-MPK3/6-PUCHI cascade.

摘要

根系结构对于植物适应不断变化的环境刺激至关重要,并且在很大程度上受侧根(LRs)影响。因此,植物如何调节侧根起始和间距是根系发育的关键要点。先前的研究表明,类受体激酶7(RLK7)及其配体LBD16的靶标2(TOLS2)控制侧根的起始和间距。然而,RLK7对TOLS2信号的感知和转导的分子机制仍有待阐明。在本研究中,我们通过研究cik突变体的表型并检测CIKs与RLK7介导的信号通路成员之间的相互作用,探索了CLAVATA3不敏感受体激酶(CIKs)在拟南芥侧根发育过程中是否为关键的信号成分。我们的结果表明,高阶cik突变体由于更多的侧根起始和有缺陷的侧根间距而产生了更多的侧根。cik突变体对施加的TOLS2肽的敏感性降低。施加TOLS2增强了CIKs与RLK7之间的相互作用以及CIKs的RLK7依赖性磷酸化。此外,转录因子PUCHI的过表达以及促分裂原活化蛋白激酶激酶4(MKK4)和MKK5的组成型激活部分挽救了cik和rlk7 - 3突变体中侧根的间距缺陷。此外,我们发现中柱鞘细胞中的生长素最大值改变了CIKs的亚细胞定位以确定侧根起始细胞。这些发现揭示了CIKs和RLK7共同发挥作用以感知TOLS2信号,并通过MKK4/5 - MPK3/6 - PUCHI级联反应调节侧根起始和间距。

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