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NAT1-bHLH110-CER1/CER1L模块调控水稻的耐热性。

The NAT1-bHLH110-CER1/CER1L module regulates heat stress tolerance in rice.

作者信息

Lu Hai-Ping, Liu Xue-Huan, Wang Mei-Jing, Zhu Qiao-Yun, Lyu Yu-Shu, Xu Jian-Hang, Liu Jian-Xiang

机构信息

State Key Laboratory of Plant Environmental Resilience, College of Life Sciences, Zhejiang University, Hangzhou, China.

School of Life Sciences, Fudan University, Shanghai, China.

出版信息

Nat Genet. 2025 Feb;57(2):427-440. doi: 10.1038/s41588-024-02065-2. Epub 2025 Jan 14.

Abstract

Rice production is facing substantial threats from global warming associated with extreme temperatures. Here we report that modifying a heat stress-induced negative regulator, a negative regulator of thermotolerance 1 (NAT1), increases wax deposition and enhances thermotolerance in rice. We demonstrated that the C2H2 family transcription factor NAT1 directly inhibits bHLH110 expression, and bHLH110 directly promotes the expression of wax biosynthetic genes CER1/CER1L under heat stress conditions. In situ hybridization revealed that both NAT1 and bHLH110 are predominantly expressed in epidermal layers. By using gene-editing technology, we successfully mutated NAT1 to eliminate its inhibitory effects on wax biosynthesis and improved thermotolerance without yield penalty under normal temperature conditions. Field trials further confirmed the potential of NAT1-edited rice to increase seed-setting rate and grain yield. Therefore, our findings shed light on the regulatory mechanisms governing wax biosynthesis under heat stress conditions in rice and provide a strategy to enhance heat resilience through the modification of NAT1.

摘要

水稻生产正面临着与极端温度相关的全球变暖带来的重大威胁。在此,我们报告称,对一种热应激诱导的负调控因子——耐热性负调控因子1(NAT1)进行改造,可增加蜡质沉积并增强水稻的耐热性。我们证明,C2H2家族转录因子NAT1直接抑制bHLH110的表达,而bHLH110在热应激条件下直接促进蜡质生物合成基因CER1/CER1L的表达。原位杂交显示,NAT1和bHLH110主要在表皮层表达。通过使用基因编辑技术,我们成功地使NAT1发生突变,以消除其对蜡质生物合成的抑制作用,并在常温条件下提高了耐热性而不影响产量。田间试验进一步证实了经NAT1编辑的水稻提高结实率和谷物产量的潜力。因此,我们的研究结果揭示了水稻在热应激条件下蜡质生物合成的调控机制,并提供了一种通过改造NAT1来增强耐热性的策略。

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