Liu Peipei, Shao Chunxuan, Ren Hang, Yang Wei, Duan Chenbo, Wang Yulin, Liao Liao, Wei Xiaoyu, Zhu Lingcheng, Ma Fengwang, Li Mingjun, Ma Baiquan
State Key Laboratory for Crop Stress Resistance and High-Efficiency Production/Shaanxi Key Laboratory of Apple, College of Horticulture, Northwest A&F University, Yangling 712100, Shaanxi, China.
State Key Laboratory of Plant Diversity and Specialty Crops, Wuhan Botanical Garden of Chinese Academy of Sciences, Wuhan 430074, China.
Int J Biol Macromol. 2025 May;308(Pt 2):142332. doi: 10.1016/j.ijbiomac.2025.142332. Epub 2025 Mar 26.
Malic acid, the most important organic acid component in the ripe apple fruit, is of great importance for the development of the fruit flavor and regulation of the metabolism. Previous studies have demonstrated that the P-ATPase MdMa11 plays a role in determining fruit acidity, and a total of 85 positive clones were identified using yeast one-hybrid screening based on the fragment in MdMa11 promoter. Among these positive clones, the NAM domain protein was designated as MdNAC18.1. The analysis of transgenic apple calli, fruits and tomatoes indicated that MdNAC18.1 induced the organic acids accumulation to regulate fruit acidity. Luciferase (LUC) and glucuronidase (GUS) activation assays showed that MdNAC18.1 binds to the G-box motif (5'-ACGT-3') located 5227 bp upstream of transcription initiation site of the MdMa11, thereby promoting its expression. Meanwhile, the expression of MdWRKY126, MdMDH5, MdtDT, MdMYB1, and MdVHP1 was found to be significantly increased in transgenic apple calli overexpressing MdNAC18.1 and decreased in MdNAC18.1-silenced transgenic apple calli. The G-box was identified in all these five genes. However, the GUS and LUC activation assays exhibited that MdNAC18.1 activated MdWRKY126, MdMDH5, MdtDT, and MdMYB1 expression. Our findings contribute valuable insights into the complex mechanism regulating the accumulation of malate in apple fruits.
苹果酸是成熟苹果果实中最重要的有机酸成分,对果实风味的形成和新陈代谢的调节至关重要。先前的研究表明,P型ATP酶MdMa11在决定果实酸度方面发挥作用,基于MdMa11启动子中的片段,通过酵母单杂交筛选共鉴定出85个阳性克隆。在这些阳性克隆中,NAM结构域蛋白被命名为MdNAC18.1。对转基因苹果愈伤组织、果实和番茄的分析表明,MdNAC18.1诱导有机酸积累以调节果实酸度。荧光素酶(LUC)和葡萄糖醛酸酶(GUS)激活分析表明,MdNAC18.1与位于MdMa11转录起始位点上游5227 bp处的G-box基序(5'-ACGT-3')结合,从而促进其表达。同时,在过表达MdNAC18.1的转基因苹果愈伤组织中,MdWRKY126、MdMDH5、MdtDT、MdMYB1和MdVHP1的表达显著增加,而在MdNAC18.1沉默的转基因苹果愈伤组织中表达下降。在所有这五个基因中都鉴定到了G-box。然而,GUS和LUC激活分析表明,MdNAC18.1激活了MdWRKY126、MdMDH5、MdtDT和MdMYB1的表达。我们的研究结果为苹果果实中苹果酸积累的复杂调控机制提供了有价值的见解。