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创伤通过动态激素和转录变化引发骨痂形成。

Wounding Triggers Callus Formation via Dynamic Hormonal and Transcriptional Changes.

机构信息

RIKEN Center for Sustainable Resource Science, Tsurumi, Yokohama, Kanagawa 230-0045, Japan

RIKEN Center for Sustainable Resource Science, Tsurumi, Yokohama, Kanagawa 230-0045, Japan.

出版信息

Plant Physiol. 2017 Nov;175(3):1158-1174. doi: 10.1104/pp.17.01035. Epub 2017 Sep 13.

Abstract

Wounding is a primary trigger of organ regeneration, but how wound stress reactivates cell proliferation and promotes cellular reprogramming remains elusive. In this study, we combined transcriptome analysis with quantitative hormonal analysis to investigate how wounding induces callus formation in Arabidopsis (). Our time course RNA-seq analysis revealed that wounding induces dynamic transcriptional changes, starting from rapid stress responses followed by the activation of metabolic processes and protein synthesis and subsequent activation of cell cycle regulators. Gene ontology analyses further uncovered that wounding modifies the expression of hormone biosynthesis and response genes, and quantitative analysis of endogenous plant hormones revealed accumulation of cytokinin prior to callus formation. Mutants defective in cytokinin synthesis and signaling display reduced efficiency in callus formation, indicating that de novo synthesis of cytokinin is critical for wound-induced callus formation. We further demonstrate that type-B ARABIDOPSIS RESPONSE REGULATOR-mediated cytokinin signaling regulates the expression of () and that mutations in and its homologs and cause defects in callus formation. In addition to these hormone-mediated changes, our transcriptome data uncovered that wounding activates multiple developmental regulators, and we found novel roles of ETHYLENE RESPONSE FACTOR 115 and PLETHORA3 (PLT3), PLT5, and PLT7 in callus generation. All together, these results provide novel mechanistic insights into how wounding reactivates cell proliferation during callus formation.

摘要

创伤是器官再生的主要触发因素,但创伤应激如何重新激活细胞增殖并促进细胞重编程仍然难以捉摸。在这项研究中,我们结合转录组分析和定量激素分析,研究了创伤如何诱导拟南芥()愈伤组织的形成。我们的时间过程 RNA-seq 分析表明,创伤诱导了动态的转录变化,从快速的应激反应开始,随后激活代谢过程和蛋白质合成,随后激活细胞周期调控因子。基因本体分析进一步揭示了创伤改变了激素生物合成和反应基因的表达,内源性植物激素的定量分析显示细胞分裂素在愈伤组织形成之前积累。细胞分裂素合成和信号转导缺陷的突变体在愈伤组织形成方面效率降低,表明细胞分裂素的从头合成对于创伤诱导的愈伤组织形成至关重要。我们进一步证明,B 型拟南芥反应调节剂介导的细胞分裂素信号调节()的表达,并且和其同源物和的突变导致愈伤组织形成缺陷。除了这些激素介导的变化外,我们的转录组数据还揭示了创伤激活了多个发育调控因子,我们发现乙烯反应因子 115 和 PLETHORA3(PLT3)、PLT5 和 PLT7 在愈伤组织生成中的新作用。总之,这些结果为创伤如何在愈伤组织形成过程中重新激活细胞增殖提供了新的机制见解。

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