miR156b 靶向 VvSBP8/13 在脱落酸信号下游发挥作用,调节干旱条件下葡萄果实中花青素的生物合成。

IF 7.6 Q1 GENETICS & HEREDITY 园艺研究(英文) Pub Date : 2024-01-02 eCollection Date: 2024-02-01 DOI:10.1093/hr/uhad293
Shuihuan Guo, Meng Zhang, Mingxin Feng, Guipeng Liu, Laurent Torregrosa, Xiaoqing Tao, Ruihua Ren, Yulin Fang, Zhenwen Zhang, Jiangfei Meng, Tengfei Xu
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引用次数: 0

摘要

花青素是葡萄浆果和葡萄酒的主要颜色成分。在栽培实践中,适度缺水可促进红葡萄果皮中花青素的积累。我们之前的研究表明,脱落酸(ABA)在这一过程中起着关键作用。在这里,我们发现了一种微RNA--vv-miR156b,它在葡萄浆果中产生,以应对干旱胁迫,同时增加花青素含量和生物合成结构基因转录本。相比之下,vv-miR156b 短串联靶标模拟(STM)功能缺失胼胝体表现出相反的表型。体内和体外实验结果表明,ABA 信号调控转录因子 VvAREB2 可直接与 MIR156b 启动子的 ABA 响应元件(ABRE)结合,并激活 miR156b 的表达。此外,两个 miR156b 下游靶标 VvSBP8 和 VvSBP13 在它们的过表达株中表现出葡萄花青素含量的降低,但在它们的 CRISPR 编辑株中却出现了相反的结果,花青素含量的降低在 miR156b 和 SBP8/13 双过表达株中得到了挽救。我们进一步证明,编码转录抑制因子的 VvSBP8 和 VvSBP13 都有足够的能力与 VvMYC1 和 VvMYBA1 相互作用,从而干扰 MYB-bHLH-WD (MBW)重复转录复合物的形成,导致花青素生物合成受到抑制。我们的研究结果表明,ABA 信号与 miR156-SBP-MBW 复合物调控模块在驱动干旱诱导的葡萄浆果花青素积累方面存在直接的功能关系。
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miR156b-targeted VvSBP8/13 functions downstream of the abscisic acid signal to regulate anthocyanins biosynthesis in grapevine fruit under drought.

Anthocyanins are the primary color components of grapevine berries and wines. In cultivation practices, a moderate water deficit can promote anthocyanin accumulation in red grape skins. Our previous study showed that abscisic acid (ABA) plays a key role in this process. Herein, we identified a microRNA, vv-miR156b, that is generated in grapevine berries in response to drought stress, along with increasing anthocyanin content and biosynthetic structural gene transcripts. In contrast, vv-miR156b short tandem target mimic (STTM) function-loss callus exhibits the opposite phenotype. Results from in vivo and in vitro experiments revealed that the ABA-signaling-regulated transcription factor VvAREB2 binds directly to the ABA-responsive element (ABRE) of the MIR156b promoter and activates miR156b expression. Furthermore, two miR156b downstream targets, VvSBP8 and VvSBP13, exhibited reduced grape anthocyanin content in their overexpressors but there was a contrary result in their CRISPR-edited lines, the decrease in anthocyanin content was rescued in miR156b and SBP8/13 double overexpressors. We further demonstrated that both VvSBP8 and VvSBP13, encoding transcriptional repressors, displayed sufficient ability to interact with VvMYC1 and VvMYBA1, thereby interfering with MYB-bHLH-WD (MBW) repeat transcriptional complex formation, resulting in the repression of anthocyanin biosynthesis. Our findings demonstrate a direct functional relationship between ABA signaling and the miR156-SBP-MBW complex regulatory module in driving drought-induced anthocyanin accumulation in grape berries.

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