The transcription factor TGA2 orchestrates salicylic acid signal to regulate cold-induced proline accumulation in Citrus

Wei Xiao, Yang Zhang, Yue Wang, Yike Zeng, Xiangming Shang, Lin Meng, Yu Zhang, Tian Fang, Peng Xiao, Jing Qu, Yilei Wang, Min Wang, Chunlong Li, Ji-Hong Liu
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Abstract

Plants subjected to cold stress have been observed to accumulate proline, but the underlying regulatory mechanism remains to be elucidated. In this study, we identified a pyrroline-5-carboxylate synthetase (P5CS)-encoding gene (CtrP5CS1) from trifoliate orange (Citrus trifoliata L.), a cold-hardy citrus species, as a critical gene for cold-induced proline accumulation. CtrTGA2 bound directly to the TGACG motif of the CtrP5CS1 promoter and activated its expression. Moreover, CtrTGA2 functioned positively in cold tolerance via modulation of proline synthesis by regulating CtrP5CS1 expression. Up-regulation of CtrP5CS1 and CtrTGA2 under cold stress was dependent on salicylic acid (SA) biosynthesis. CtrTGA2 directly regulated the expression of CtrICS1, a gene encoding isochorismate synthase (ICS) involved in SA biosynthesis, forming a positive feedback loop to intensify the CtrTGA2-mediated transcriptional activation of CtrP5CS1. The cold-induced SA receptor NONEXPRESSOR OF PATHOGENESIS-RELATED GENES3 (CtrNPR3) interacted with CtrTGA2 to inhibit its transcriptional activation activity; however, the inhibition was released by SA. Our results uncover the CtrTGA2-CtrP5CS1/CtrICS1 regulatory module that orchestrates the SA signal to regulate proline synthesis, giving important insights into the transcriptional mechanism underlying proline accumulation in plants under cold stress.
转录因子TGA2通过调控水杨酸信号调控冷诱导的脯氨酸积累
植物在低温胁迫下会积累脯氨酸,但其潜在的调控机制尚不清楚。在这项研究中,我们从耐寒柑橘品种三叶橙(Citrus trifoliata L.)中鉴定了一个吡咯啉-5-羧酸合成酶(P5CS)编码基因(CtrP5CS1),该基因是冷诱导脯氨酸积累的关键基因。CtrTGA2直接结合到CtrP5CS1启动子的TGACG基序上并激活其表达。此外,CtrTGA2通过调节CtrP5CS1的表达来调节脯氨酸的合成,从而在耐寒性中发挥积极作用。低温胁迫下CtrP5CS1和CtrTGA2的上调依赖于水杨酸(SA)的生物合成。CtrTGA2直接调控参与SA生物合成的异chorisate synthase (ICS)编码基因CtrICS1的表达,形成正反馈回路,强化CtrTGA2介导的CtrP5CS1的转录激活。冷诱导SA受体致病相关基因3 (CtrNPR3)与CtrTGA2相互作用抑制其转录激活活性;然而,SA释放了抑制作用。我们的研究结果揭示了CtrTGA2-CtrP5CS1/CtrICS1调控模块,该模块通过SA信号调控脯氨酸合成,为揭示低温胁迫下植物脯氨酸积累的转录机制提供了重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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