Iron Deficiency Reprograms Lateral Root Growth via TAR2-Dependent Auxin Biosynthesis in Arabidopsis.

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Budha Ratna Rav, Santosh B Satbhai
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引用次数: 0

Abstract

Auxin plays a central role in shaping root system architecture (RSA) by regulating cell division, differentiation, primary root elongation, and lateral root (LR) initiation and emergence. Iron (Fe) is an essential micronutrient required for photosynthesis, chlorophyll biosynthesis, and redox metabolism. Fe availability has a significant impact on plant health, development, and yield. Here, we investigate the role of the auxin biosynthetic gene TRYPTOPHAN AMINOTRANSFERASE RELATED2 (TAR2) in coordinating LR development and Fe homeostasis in Arabidopsis thaliana. Fe deficiency increased auxin accumulation in roots, as observed through DR5rev:GFP reporter activity, and this response required TAR2 function to drive Fe deficiency-induced modifications to RSA. The tar2-1 mutant displayed significantly reduced visible LR numbers, total LR length and LR density. Yeast one-hybrid assays identified several Fe deficiency-responsive bHLH transcription factors, including bHLH34, bHLH38, bHLH39, and PYE, that directly bind the TAR2 promoter, indicating a regulatory link between Fe signaling and auxin biosynthesis. Together, our findings support that TAR2-dependent local auxin biosynthesis is a major contributor to LR development and the adaptive reprogramming of RSA in response to Fe deficiency.

铁缺乏通过tar2依赖性生长素生物合成重编程拟南芥侧根生长。
生长素通过调节细胞分裂、分化、主根伸长和侧根(LR)的形成和萌发,在形成根系结构(RSA)中起核心作用。铁(Fe)是光合作用、叶绿素生物合成和氧化还原代谢所必需的微量营养素。铁的有效性对植物的健康、发育和产量有重要影响。在此,我们研究了生长素生物合成基因色氨酸氨基转移酶相关2 (TAR2)在拟南芥LR发育和铁稳态协调中的作用。通过DR5rev:GFP报告活性观察到,缺铁增加了根中生长素的积累,这种反应需要TAR2功能驱动缺铁诱导的RSA修饰。tar2-1突变体的可见LR数、总LR长度和LR密度显著降低。酵母单杂交实验发现了几种铁缺乏反应的bHLH转录因子,包括bHLH34、bHLH38、bHLH39和PYE,它们直接结合TAR2启动子,表明铁信号传导与生长素生物合成之间存在调控联系。总之,我们的研究结果支持了依赖于tar2的局部生长素生物合成是LR发育和RSA响应铁缺乏的适应性重编程的主要贡献者。
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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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