TaFAR5-TaFAR3 module regulates cuticular wax biosynthesis and drought tolerance in wheat

IF 8.1 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2025-08-31 DOI:10.1111/nph.70512
Yuling Liu, Bin Chen, Zhen Qin, Ping Jiang, Yanyan Yang, Chen Wang, Tongfang Xing, Fangfang Li, Linying Du, Shumin Li, Xiaoke Zhang, Xiaojun Nie, Zhensheng Kang, Hude Mao
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引用次数: 0

Abstract

  • Plant cuticular waxes function as a protective barrier to mitigate environmental stresses, especially water deficit, although the molecular mechanisms and natural genetic variations underlying wax accumulation in crops remain unclear.
  • Our genome-wide association study (GWAS) of the contents of cuticular wax components in wheat seedlings demonstrated that allelic variations in TaFAR5, encoding a fatty acyl-CoA reductase, contribute to the differences in leaf cuticular wax accumulation. Molecular and transgenic analyses revealed that variations in the TaFAR5 promoter affect the binding affinity between cis-regulatory elements and several transcription factors, including TaLBD16, TaERF12, TaNAC2, TaWRKY2, TaMYBC1, and TaNAC6, consequently modulating TaFAR5 expression.
  • Interestingly, allelic variations in the TaFAR5 coding sequence induce amino acid substitutions that promote interaction between TaFAR5 and TaFAR3, which in turn significantly boost biosynthesis of primary alcohol components of cuticular wax. Moreover, TaFAR5 or TaFAR3 knockout attenuates drought stress tolerance, while their overexpression remarkably enhances drought tolerance in wheat seedlings by reducing water loss. Additionally, we found that the favorable TaFAR5 allele is widely distributed in tetraploid wheat but has limited distribution in hexaploid accessions, occurring at higher frequency in arid regions.
  • Taken together, this study demonstrates how natural variations in TaFAR5-TaFAR3 regulatory module impact leaf cuticular wax biosynthesis to confer drought tolerance in wheat.

Abstract Image

TaFAR5‐TaFAR3模块调控小麦表皮蜡质生物合成和耐旱性
植物角质层蜡质作为一种保护屏障,可以缓解环境胁迫,尤其是水分亏缺,但目前尚不清楚植物角质层蜡质积累的分子机制和自然遗传变异。我们对小麦幼苗角质层蜡成分含量的全基因组关联研究(GWAS)表明,编码脂肪酸酰辅酶a还原酶的TaFAR5等位基因变异导致了叶片角质层蜡积累的差异。分子和转基因分析表明,TaFAR5启动子的变异会影响顺式调控元件与几种转录因子(包括TaLBD16、TaERF12、TaNAC2、TaWRKY2、TaMYBC1和TaNAC6)的结合亲和力,从而调节TaFAR5的表达。有趣的是,TaFAR5编码序列的等位基因变异诱导氨基酸取代,促进TaFAR5和TaFAR3之间的相互作用,从而显著促进角质层蜡中伯醇成分的生物合成。此外,TaFAR5或TaFAR3基因敲除降低了小麦幼苗的抗旱性,而它们的过表达通过减少水分损失显著提高了小麦幼苗的抗旱性。此外,我们发现TaFAR5等位基因在四倍体小麦中广泛分布,而在六倍体小麦中分布有限,在干旱区出现频率较高。综上所述,本研究证明了TaFAR5 - TaFAR3调控模块的自然变异如何影响小麦叶片角质层蜡的生物合成,从而赋予小麦耐旱性。
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
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